Norgen Newsletter 1

Bacterial Extracellular Vesicles: An Emerging Field in Microbiology

In recent years, the scientific community has begun to view bacteria not only as disease-causing microorganisms but also as biological systems capable of communication. This shift in understanding is largely due to the discovery of small lipid-membrane structures known as bacterial extracellular vesicles (bEVs).

These vesicles, ranging from 30–400 nm in size, are actively secreted by bacteria and carry molecules such as DNA, RNA, proteins, and lipids. Thanks to these components, bacteria can communicate with one another and with host cells—acting much like intercellular messengers.

Bacterial Extracellular Vesicles: An Emerging Field in Microbiology

In recent years, the scientific community has begun to view bacteria not only as disease-causing microorganisms but also as biological systems capable of communication. This shift is primarily driven by the discovery of small lipid-membrane structures known as bacterial extracellular vesicles (bEVs).

These 30–400 nm vesicles are actively released by bacteria and carry DNA, RNA, proteins, and lipids. Through these molecules, bacteria communicate with each other and with host cells—acting much like message carriers between cells.


Growing Interest in Research

bEVs have rapidly become a focal point in both fundamental microbiology and applied biotechnology. These vesicles play critical roles in:

  • The transfer of antibiotic resistance genes

  • Host–pathogen interactions

  • Maintenance of microbiome balance

  • Diagnostic and therapeutic development

With these features, bEVs are seen not only as tools for understanding bacterial behavior but also as keys to next-generation diagnostic and therapeutic approaches.

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Challenge: Reliable Isolation

However, isolating bEVs remains a major challenge for many researchers. Traditional methods such as ultracentrifugation or protein precipitation are time-consuming, costly, and have low reproducibility. This limits the reliability of studies aiming to obtain EVs from different bacterial species.

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Letgen’s Solution: The World’s First and Only Bacterial EV Isolation Kit

In response to these challenges, the Norgen Bacterial Extracellular Vesicle Isolation Kit was developed—the first and only kit providing rapid, high-yield EV isolation directly from bacterial culture media.

🔍 Key Features

✅ Purification of intact EVs in the 30–400 nm size range
✅ Flexible sample input volumes (5 mL – 35 mL)
✅ No ultracentrifugation, special syringes, or precipitation steps
✅ Fast, reproducible, slurry-based system
✅ Pure EVs compatible with downstream applications (qPCR, NGS, etc.)

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Performance analyses of the kit demonstrate a clear increase in microRNA yield with larger culture volumes, along with lower Cq values and higher bacterial RNA recovery.


A New Era in bEV Science

This kit marks a new era in bacterial EV research, fully separating it from mammalian EV isolation workflows and offering a bacteria-focused, standardized solution. Researchers studying microbiomes, pathogen interactions, and antibiotic resistance can now work faster and more reliably.

👉 Norgen Bacterial Extracellular Vesicle Isolation Kit — the world’s first and only commercial solution for bacterial EV research.

📦 Order now for Turkey and Azerbaijan:
🔗 www.letgenbio.com
📩 info@letgenbio.com
📞 +908504412987

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Gelecegin Tibbi ve Daha Fazlasi Eksozom Kesif Serimiz Basliyor

The molecular language of cancer is now better understood. One of the silent but powerful words in this language is undoubtedly exosomes. These microscopic vesicles, 30-150 nanometers in size, reveal how tumor cells communicate with their environment, evade the immune system and organize metastasis.


Exosomes To explain its impact with a few scientific findings;


- Increased Proliferation


Lin et al. showed that exosomes derived from adipose tissue-derived mesenchymal stem cells (ADMSC) increased cell proliferation by activating the Wnt/β-catenin signaling pathway in MCF7 breast cancer cells (Lin et al., 2013).


- Immune Suppression


(2023) demonstrated that exosomes promote immune suppression in the tumor microenvironment by directing macrophages to the M2 phenotype. This plays an important role in resistance to immunotherapies (Zhu et al., 2023).


- Metabolic Reprogramming


Wang et al. (2020) showed that exosomes trigger metabolic reprogramming by altering the energy production pathways of tumor cells. This is a critical factor in providing a growth advantage, especially for aggressive tumors (Wang at al., 2020)


- Angiogenesis and Hypoxia Adaptation


Exosomes promote new vessel formation by transporting angiogenic factors such as VEGF and trigger adaptation processes that facilitate cell survival in hypoxic conditions (Teng et al., 2018).



Scientifically, it is now undisputed that exosomes carry a wealth of information. But isolating them in the laboratory in a pure, intact form, suitable for analysis or cancer diagnosis, is still a highly complex process.


Because it is in isolation:


-Lipid contamination can severely impair RNA purity, especially in samples such as plasma and adipose tissue.
-The high protein content clouds the analysis results.
-Conventional precipitation methods are efficient, but they often result in non-specific particles.
- "Traditional gold standards" such asultracentrifugation offer practices that are difficult to achieve in terms of both time and equipment.


And perhaps most importantly: The quality of the isolated material determines the accuracy of all downstream analyses. Behind a qPCR data or miRNA sequencing analysis often lies an unnoticed isolation success (or failure).


Traditional isolation methods can yield time-consuming and variable results. At this point, theinnovative kits developed by Norgen Biotek offer revolutionary solutions in exosome isolation .


-High Purity and Efficiency: Patented Silicon-carbide (SiC) spin column technology enables high purity and efficient exosome and RNA isolation.
-Safety: Provides safe isolation without the need for organic solvents such as phenol and chloroform, Proteinase K treatment or carrier molecules.

- Preservation of Exosome and RNA Integrity: Isolated exosomes and RNA are of high integrity and purity, supporting reliable data acquisition in downstream applications such as RT-qPCR, NGS, WB, NTA.


-Flexible Input Volume: Ensures high throughput even from very low sample volumes. Compatible with flexible sample volumes from 50 µL to 10 mL.
-Specialized kit constructs makeit possible to isolate exosomal RNA and free circulating RNA in separate fractions.

- Time and Equipment Savings: The kits offer a fast and practical isolation process without the need for specialized equipment.


-Wide Product Range: Offers optimized kit options for many different materials

As Letgen Biotechnology, we are proud to offer these superior kits from NorgenBiotek, our distributor in Turkey and Azerbaijan. With our technical consultancy and implementation supportWe help you achieve the best results in your exosome research. Norgen's exosome isolation kits are optimized for many different biological materials such as urine, saliva and blood. There are even kits developed to isolate exosomes from cell cultures that you can use for your in vitro studies. However, this week, you can examine the figure below, which includes the features of 3 of the kits we have selected from the kits used in plasma/serum samples, which are the most preferred among liquid biopsy samples.


You can contact us for more information and support: info@letgenbio.com



Reference:


Lin R, Wang S, Zhao RC. Exosomes from human adipose-derived mesenchymal stem cellspromote migration through Wnt signaling pathway in a breast cancer cell Model. Mol Cell Biochem. 2013;383(1-2):13–20. doi:10.1007/s11010-013-1746-z.


Dong Y, Fu Y, Cai Z, Dai Y, He Z. Recent advances in adipose-derived mesenchymal stem cellexosomes: Immunomodulatory properties and therapeutic applications. Front Immunol. 2025;16:1525466. doi:10.3389/fimmu.2025.1525466.


Zhang Y, Wang X, Wang J, Zhang X, Wang Y. Exosome-mediated metabolic reprogramming: the emerging role in tumor microenvironment remodeling and cancer progression. SignalTransduct Target Ther. 2020;5(1):242. doi:10.1038/s41392-020-00359-5.


Zhou C, Huang YQ, Da MX, Jin WL, Zhou FH. Adipocyte-derived extracellular vesicles: Bridging the communications between obesity and tumor microenvironment. DiscoverOncology. 2023;14(1):92. doi:10.1007/s12672-023-00704-4.


Wang J, Wu Y, Guo J, Fei X, Yu L, Ma S. Adipocyte-derived exosomes promote lung cancermetastasis by increasing MMP9 activity via transferring MMP3 to lung cancer cells. Oncotarget. 2017;8(47):81880–81891. doi:10.18632/oncotarget.18737.

Rochetan Atik Su Gozetiminde Yeni Standart Digital LightCycler dPCR Sistemi

While traditional epidemiological methods often focus on symptomatic individuals, asymptomatic carriers in the wider society can be overlooked. The biological traces that individuals unknowingly leave in their daily lives constitute the invisible health map of society. When read with the right tools, this map opens the door to a world where infections can be stopped before they spread, health systems can become proactive, and even future outbreaks can be predicted in advance. The key to this door is Roche Digital LightCycler® dPCR System technology .

Wastewater offers a large, population-based, passive observation area that is beyond the reach of individual testing. Biological data collected from the entire population includes the viral load, whether symptomatic or asymptomatic. This is where the power of digital PCR technology makes a difference, as it can reliably detect even the weakest molecular signalswithin this complex matrix. In this way, it not only monitors public health, but also turns it into a source of data that can be used to generate strategic insights.

As an authorized dealer of Roche DiagnosticsLightCycler® product group, which is considered a global reference in advanced molecular technologies, Letgen Biotechnology not only offers advanced technology solutions, but also provides scientific guidance, technical consultancy and project-oriented support to researchers in the field applications of these systems. From universities to public institutions, from the private sector to environmental health, many stakeholders can find direction in accessing these advanced molecular technologies through Letgen Biotechnology.

Academic and scientific institutions that want to conduct research can request supportfrom us in the process of integrating digital PCR technology into their projects ; thus, a guiding partnership can be established in accessing and applying the technology.As Letgen Biotechnology, we are proud to be not only a product provider but also a strategic solution partner that contributes to scientific production.

As Letgen, we are able to design unique primer-probe sets and method optimization for microorganisms requested in wastewater sampling. In this way, it becomes possible to analyze the targeted pathogens with high sensitivity and reliability on the Roche Digital LightCycler® dPCR system. In addition, withmultiplex panels developed specifically for user needs , multiple target microorganisms can be detected simultaneously in a single reaction, which offers significant advantages in terms of both time savings and resource optimization .

Roche Digital LightCycler® dPCR High Sensitivity Microorganism Analysis in Wastewater with

In molecular biology, precision, reliability and versatility only make sense when they meet the right technology. At this point, Roche's Digital LightCycler® dPCRSystem goes beyond being just a PCR platform and becomes a reference point in epidemiological surveillance.

Digital PCR is the future. And it is Roche's engineering vision that shapes this future. Here are 6 key capabilities that differentiate this system from the competition and make it unique:

- Strong Resistance to Inhibitors: It is difficult to get reliable results in complex and inhibitor-rich samples such as wastewater. The microreaction-based system developed by Roche minimizes this obstacle and allows you to access the data directly. Molecular clarity no longer depends on sample quality.

- High Input Volume (Large Input Volume): More samples, more confidence. Thanks to the system's high-volume analysis capacity, even low-density viral loads are not missed. This is especially critical in capturing traces from asymptomatic individuals.

- High Sensitivity (High Sensitivity): Detecting preclinical dissemination is no longer a dream. This system, which can detect even low copy numbers of nucleic acids with pinpoint accuracy, serves as a biological radar for early warning mechanisms.

- 3 Different Plate Configurations: Flexibility leads to success in the field. With three different plate options that can be optimized for different applications and sample types, the system adapts to your workflow, not your laboratory environment.

- Advanced Multiplexing with Optical Channel : The digital LightCycler® makes it possible to analyze multiple pathogens simultaneously in a single reaction. Respiratory viruses such as SARS-CoV-2, influenza A/B, RSV can all be reliably measured in the same test.

- 5X Concentrated Master Mix: This condensed formula allows you to load more samples per reaction. Result. Increased sensitivity and stronger statistical reliability.

dPCR-based wastewater surveillance is no longer just a laboratory application - it is a science-based early warning system for public health crises. It is a powerful bridge between different sectors and disciplines, putting data at the center of decision-making.

🎓 For Academic and Scientific Circles

Data sets that can analyze the burden of infection at the societal level over time and space are no longer a dream. dPCR technology enables researchers to go beyond classical modeling and conduct real-time epidemiological analyses. This means not only understanding the spread, but predicting it.

🏛️ For Public Laboratories and Health Authorities

Wastewater surveillance supported by dPCR reflects the pathogen burden in the community independently of traditional testing systems. This enables prioritized response, effective use of resources and proactive outbreak management. Gone are the days of decision-making based on intuition, not knowledge

🧬 For the Biotechnology and Environmental Health Sector

With its high sensitivity, inhibitor resistance and multiplexing capabilities, dPCR is not just an analysis method, but an R&D engine for product development, test kit design and new healthcare technologies. It also provides a strong basis for sustainability-oriented public-private collaborations.

📍 A concrete example of this multidisciplinary approach is the US Centers for Disease Control and Prevention's (CDC) National Wastewater Surveillance System (NWSS) program. It is a global benchmark for integrating dPCR technology into public health infrastructure - and many countries are now starting to integrate similar systems into their national health policies. (See the visualization of the "dPCR-Based Wastewater Surveillance Cycle" below)

You can contact us for detailed information or order.

info@letgenbio.com

+90 850 441 2987

+90 535 830 05 60

Gelecegin Dizileme Platformu Roche Genisleme Yoluyla Dizileme Sequencing by Expansion SBX

Genetic sequencing has become an essential tool in a wide range of applications, from scientific research to clinical diagnosis. However, existing technologies still face significant trade-offs between speed, accuracy, cost and flexibility. This is whereSequencing by Expansion ( SBX) technology developed by Roche comes into play. SBX both offers a solution to the challenges in molecular biology and ushers in a new era in sequencing processes.

How Does SBX Technology Work?

Unlike conventional sequencing systems, SBX (Sequencing by Expansion) technology works with a CMOS sensor-based system that synthesizes and reads Xpandomer, a special molecule that represents the DNA sequence, rather than reading it directly.

1. Preparation of Target DNA

- One of the key features of SBX is that DNA is extracted from the sample and used directly for Xpandomer synthesis. The absence of fragmentation and adapter ligation steps in traditional methods makes this technology different.

2. Xpandomer Synthesis

This is where SBX's key difference begins. The synthesis of Xpandomer, a copy of the DNA sequence, using X-NTPs, the enzyme XP Polymerase and PEM molecules is the heart of SBX. This step allows the DNA information to be encoded into a different molecular form, the Xpandomer.

3. Expansion Process

The physical enlargement of the Xpandomer is a critical step in making signals easier and clearer to read . This chemical expansion in an acidic environment is a key feature from which the technology gets its name.

4. Loading to CMOS Sensor Module

A CMOS sensor consists of about 8 million microwires. This means that millions of molecules can be sequenced simultaneously. The insertion of extended Xpandomer molecules into these microwells is a critical step for reading large amounts of data in parallel. The CMOS sensor detects the signals emitted from the Xpandomer molecules with high sensitivity.

5. Electrical Readout - Sequencing Begins

Detection and recording of electrical signals generated by the interaction of Xpandomers with sensors is the stage where the sequencing process takes place. The high resolution of the CMOS sensor allows for precise signal detection.

6. Data Analysis

The processing of the acquired electrical signals to reconstruct the DNA sequence is the final, information-converting stage of the sequencing process. The potential for real-time data acquisition and high accuracy increases the efficiency of this stage.

Why the Sequencing Platform of the Future?

Although next-generation sequencing (NGS) technologies have made great advances in recent years, existing systems still have some fundamental limitations: high cost, long processing times, limited accuracy rates and lack of scalability. The SBX technology developed by Roche stands out with its innovative structure targeting these limitations.

Comparing SBX with the General Characteristics of Other Platforms:

-Competitor I offers high sensitivity with short read lengths but is limited by time-consuming preparation processes and optics-based readout systems.-Competitor ON has the advantage of long read capacity and portability, but signal-to-noise separation is poor and raw read accuracy is low.-Competitor P is particularly successful with complex genomes with its HiFi (high-accuracy long read) technology, but the instrument cost and run time are high.-The competing IO is suitable for targeted analysis, but its pH-based signaling system can be problematic, especially in GC-intensive areas.

SBX combines the advantages of existing sequencing platforms while creating a new alternative in areas where they do not offer a solution. This technology

- He works much more efficiently than Rival I during the preparation process,- He's outpacing rival ON in speed ,- It competes with Rival P in accuracy ,- Superior flexibility in scalability than competitive IO.

Which Biological Questions Does It Solve?

SBX technology goes beyond the boundaries of conventional sequencing platforms and makes a difference, especially in the following areas:

-Oncology: Rapid and sensitive genetic profiling of tumor samples.-Rare Diseases: High accuracy for detection of low-frequency variants.-Neurodegenerative Diseases: Broad analysis from single gene level mutations to complex structural variations.-Liquid Biopsy: Fast response time for samples containing low amounts of DNA.-Clinical Research: Efficiency that reduces project time and cost.

SBX technology is an innovation with the capacity to go beyond conventional sequencing platforms and create the genetic analysis infrastructure of the future. Although it will be available in 2026, it has already aroused great interest in scientific circles. Discovering this technology early can take your research one step further.

As Letgen Biotechnology, we closely follow the technologies that remove the barriers to genetic discoveries, and we care about supporting solutions that will take scientists' research one step further.

👉 If you want to take a look at the 10-year development process and technical details of SBX technology: 🔗
More about SBX Technology

NEAT1 ve Genom Stabilitesi DNA Hasar Yanitinda Yeni Bir Perspektif

A new study reveals the surprising role of NEAT1(Nuclear Paraspeckle Assembly Transcript 1) in maintaining the genetic integrity of cells and provides a whole new perspective on the #DNA damage response.

NEAT1 gene transcripts are overexpressed in many tumors and respond to genotoxic stress. However, the mechanism linking NEAT1 to DNA damage response remains unclear. In this study;

The effects of DNA double-strand breaks (DSBs) on genome stability allow us to better understand the role of NEAT1 in the DNA damage response (DDR). Research shows that DNA damage increases NEAT1 levels and N6-methyladenosine (m6A) signaling. This process triggers changes in NEAT1 structure and promotes NEAT1 accumulation at promoter-associated DSBs and DSB signaling.

NEAT1 depletion increases DNA damage by inhibiting DSB foci formation. Through RNA methylation provided by METTL3, NEAT1 interaction with the chromodomain helicase DNA binding protein 4 (CHD4) enhances the DDR mechanism by fine-tuning histone acetylation.

https://genesdev.cshlp.org/content/38/17-20/915

These findings emphasize the genome-protective role of NEAT1 under genotoxic stress.

NEAT1 plays a critical role in promoting the DNA damage response (DDR) under genotoxic stress. It maintains genome stability by promoting structural changes and DSB signaling through m6A methylation.

#You can contact us for products that help you shape the future with these discoveries that shed light on cancer research and DNA repair mechanisms.

Kanatli Sektorunde Tani ve Biyoguvenlik

Poultry diseases often progress silently. A small drop in production, a few days of increased mortality or missed clinical signs can actually indicate the onset of a much more serious infection in the flock. In particular, diseases such as AvianInfluenza (AI), Newcastle Disease(NDV) and Infectious Bursal Disease (IBDV) are threats that directly affect not only animal health but also business sustainability, trade and reputation. According to the World Organization for Animal Health (WOAH), more than 250 million poultry were culled worldwide due to avian influenza in 2023 alone. This has made the economic and epidemiological impacts of Avian Influenzamore critical than ever. (Source: WOAH, 2023)

The common feature of these diseases is that they spread rapidly and cause chain losses if not detected early. However, if the disease can be recognized before it shows clinical symptoms, it can be controlled without a crisis. At this point, ELISA tests play a critical role in identifying risk areas by assessing the level of immunity on a herd basis, while molecular methods such as Real-Time PCR (qPCR) are sensitive and reliable enough to detect viruses even before symptoms begin. The 2013 study by Spackman et al. clearly demonstrated how the use of RT-PCR as the reference method for AI detection revolutionized the diagnostic process. Likewise, the OIE's 2023 guidelines and EFSA's 2022 reports recommend integrating these tests into disease control programs. The H5N1 and H7N9 subtypes in particular pose a high risk to both animal and public health. These subtypes require joint intervention in both veterinary and human health due to their zoonotic potential. (CDC, 2023; FAO, 2022)

At this point, as Letgen Biotechnology, we stand out with the solutions we offer. Turkey, which we represent Innovative Diagnostics brand, we offer a broad diagnostic portfolio including ELISA and qPCR kits. IDVET ELISA and Letgen qPCR test systems are developed in accordance with protocols used in reference laboratories in many countries, including the European Union. This enables Turkish manufacturers to meet global quality, while at the same time contributing to the spread of data-driven decision-making culture in the industry.

The right diagnosis at the right time sets the direction not only for individual animals, but for the entire herd and production chain. Unnecessary antibiotic applications, incorrect vaccinations, delayed quarantine decisions or missed outbreaks are often caused by incomplete or late diagnosis. However, with standardized and validated diagnostic kits, field data and laboratory accuracy can be combined. This secures not only health management, but also economic and logistical decisions.

Biosecurity is often equated with physical measures, whereas true biosecurity starts with data-driven decisions. The biggest difference is seen in businesses that prioritize diagnosis. Because diagnosis is not only a diagnostic tool, but also a control system that guides the future of production. Today, many countries have procedures for the circulation of commercial products that depend on health certificates and negative test results. This means that diagnostics are of strategic value not only for veterinary services, but also for exports and market access .

Data, not intuition, now speaks in poultry health. Success in the fight against diseases lies not only in treating them, but also in seeing them before they occur. Thanks to science-based diagnostic systems, both animal welfare is protected and the producer's hand is strengthened. Seeing the invisible is possible with the right systems. And this is decisive not only for health, but for the entire future of the sector.

References Used:

- Spackman, E. et al. (2013) "Development of real-time RT-PCR for the detection of AvianInfluenza virus." Source: Avian Diseases Journal

- WOAH (World Organization for Animal Health), 2023 "Global situation of avian influenza(HPAI) - Summary 2023." Note: It is stated that more than 250 million birds were culled due to avian influenza in 2023. Web:
www.woah.org

- OIE Terrestrial Manual (World Organization for Animal Health), 2023 "Manual of Diagnostic Tests and Vaccines for Terrestrial Animals - Avian Influenza Chapter." Web: OIE - Terrestrial Manual

- EFSA (European Food Safety Authority), 2022 "Avian influenza Overview December 2021 - March 2022." Web: EFSA Journal

- CDC (Centers for Disease Control and Prevention), 2023 "Avian Influenza in Birds."It was emphasized that especially H5N1 and H7N9 subtypes carry zoonotic risk. Web:
www.cdc.gov/flu/avianflu

- FAO (Food and Agriculture Organization), 2022 "FAO recommendations on avianinfluenza surveillance and control." Web: www.fao.org

Phage DNA Izolasyonu

Advantages and Unique Aspects

Unrivaled Performance: Why? Norgen Biotek ?

As the depth of your bacteriophage research increases, the importance of accurate and efficient DNA isolation increases. As Letgen Biotechnology, we aim to bring you solutions that will make this process faster and more efficient. Norgen Phage DNA Isolation Kit not only provides high quality results, but also saves time and effort in your research.

Fast and Efficient DNA Isolation

Norgen Phage DNA Isolation Kit is a unique product that completes DNA isolation from bacteriophages in just 45 minutes. Using patented silicon-carbide-based column technology, it allows isolation without the need for hazardous chemicals such as phenol and chloroform, which are both harmful to health and can cause inhibition in downstream processes. Thus, it offers a safer, practical and reliable process. In addition to achieving fast results, it guarantees high efficiency at every step.

One of the biggest advantages of this kit is that it offers a wide range of applications. It provides high quality and clean DNA for many advanced analyses such as PCR, qPCR, cloning, NGS sequencing, Southern Blotting. Especially for functional analysis of bacteriophages, the cleanliness and efficiency offered by this kit provides the opportunity to obtain robust and reliable results.

Why is it Different from Others?

While there are many phage DNA isolation kits on the market, the unique results provided by the Norgen Phage DNA Isolation Kit make it stand out. It provides lower host DNA contamination than other kits, making it possible to obtain phage DNA in pure and high yields. This feature is critical for bacteriophage studies because high purity phage DNA is the basis for reliable assays.

Another important difference is the ease of use of the kit. Offering fast and effective isolation, this kit is also user-friendly. The protocol is simple to follow, so you can achieve perfect results every time, regardless of your level of experience.

As Letgen Biotechnology, we have experienced the fast, efficient and reliable results and user satisfaction provided by the Norgen Phage DNA Isolation Kit. Therefore, we believe that it is an indispensable tool in bacteriophage studies. With its practicality and superior efficiency, this kit is an ideal solution for use in all kinds of scientific studies and industrial research involving bacteriophages. Norgen is the reliable and unrivaled choice for high quality DNA isolation.

You can contact us for more information or to place an order.

info@letgenbio.com

Virusler Gorulemez ama Olculebilir

Viruses are among the most interesting structures that question the boundary between the living and the non-living in biology. These organisms, which carry their genetic material in a protein sheath, cannot reproduce on their own; they can survive by utilizing the metabolic mechanisms of host cells. With these characteristics, they have inspired not only infections but also fundamental research in molecular biology.

Throughout history, humanity has witnessed many pandemics. Following the Spanish Flu in 1918, the HIV/AIDS pandemic and the H1N1 pandemic in 2009, the SARS-CoV-2 pandemic that emerged in 2019 has radically changed healthcare systems and scientific priorities on a global scale. COVID-19, in particular, has once again highlighted the need to diagnose viruses at the molecular level and the need for precision in diagnostic technologies. In the first months of the pandemic, there was a huge mismatch between the rate of spread of the virus and diagnostic capacity, clearly demonstrating how critical accurate, rapid and reliable molecular diagnostic methods are.

Clinical symptoms are often insufficient for the detection of viral infections. For this reason, the identification of infections at the molecular level is indispensable both for the diagnosis of diseases and for monitoring the spread. The first and most critical step in the molecular diagnostic process is the reliable isolation of RNA or DNA, the genetic material of the virus. The success of the diagnosis directly depends on the purity and integrity of the nucleic acid obtained at this stage.

At this point, Norgen Biotek and Roche Diagnostics offer reliable and effective solutions for researchers with their kits for viral nucleic acid isolation. Norgen's spin column-based isolation kits are characterized by their flexibility to work with different sample types (such as blood, plasma, saliva, urine) and their high efficiency. Thanks to their patented resins, they offer the opportunity to isolate RNA and DNA simultaneously, which means time savings and increased analysis sensitivity. Roche's products such as Roche's High Pure Viral Nucleic Acid Kit offer reliability in downstream analysis by providing effective isolation even in viral samples with low copy number, thanks to their strong lysis buffers and high binding capacity glass fiber filters. The products of both brands are differentiated from their competitors by their success in removing inhibitors and ease of integration into automation systems. Therefore, the isolation process, which forms the basis of molecular diagnostics, is the first step to error-free and reproducible results.

Following isolation, qPCR (quantitative polymerase chain reaction) and dPCR (digital PCR) technologies are now the two pillars of viral diagnostics. qPCR enables amplification of target nucleic acid sequences and simultaneous quantification through fluorescent signals. Its high specificity and sensitivity have made it the primary diagnostic method during pandemics. However, its sensitivity may be limited at low viral loads as qPCR assays usually quantify on standard curves.

To overcome these limitations, digital PCR (dPCR) technology has been developed to split the sample into thousands of small compartments and perform separate PCR reactions in each. This allows quantification to be done in absolute terms, independent of the standard curve. Numerous studies published in PubMed show that dPCR offers significant advantages in reliably detecting SARS-CoV-2, even in presymptomatic individuals. In addition, dPCR technology is characterized by high-resolution data generation in sensitive situations such as monitoring residual viral load after treatment in chronic viral infections such as HIV, HBV and HCV.

While both methods have strong advantages in their own right, they come with some limitations depending on the application and need. qPCR is a lower-cost, high throughput technology that delivers fast results. In contrast, dPCR, while offering high sensitivity, comes with challenges such as longer analysis time, limited sample capacity and higher cost.

As theLetgen family, we know the potential of these technologies and the needs of laboratory conditions very well. For this reason, we not only offer our digital PCR infrastructure to researchers, but also produce solutions that add scientific value to your projects. By using our dPCR platform with absolute quantification power in your projects, you can interpret your data with confidence and make your analyzes more precise. You can also easily access the Roche and Norgen isolation kits you need for your viral studies on Letgen. With our fast delivery guarantee, we support the entire process without disrupting the rhythm of your research; we bring you together not only with the right product but also with the confidence that arrives on time.

Because we are more than a supplier, we are a true stakeholder in your scientific journey.

Dijital PCR Hassasiyetin Zirvesi

Digital PCR (dPCR) is a technology that enables quantitative measurement of DNA or RNA samples by precisely amplifying them. dPCR is more sensitive than conventional PCR methods and is particularly effective for difficult-to-detect analyses such as rare mutations, low copy number targets and genetic variations. This technology takes place in a large number of small reaction chambers where samples are individually split so that each target molecule is analyzed independently. This results in more precise and quantitative results.

Where the Roche Digital LightCycler® differs from its competitors is its nanowell technology and large sample capacity. Nanowell plates provide smaller-volume reaction chambers during the digital PCR process, enabling more target partitioning and thus exponentially increasing sensitivity. Thanks to high sensitivity, even challenging analyses such as rare mutations or low copy number genes are completed with more reliable and reproducible results. In addition, Roche's optimized dPCR mastermixes show superior performance even in the presence of inhibitors.

Roche's triple nanowell plates allow each DNA or RNA molecule to be isolated and analyzed separately. These plates enable reliable analysis of genetic disorders, cancer detection, prenatal testing and rare genetic variations in clinical research. Thousands of independent reaction chambers in each plate allow a large number of targets to be processed simultaneously for faster and more efficient analysis. In addition, the small reaction volume of these plates reduces reagent usage, lowering costs and resulting in a more efficient process.

The Roche Digital LightCycler® dPCR system has become an indispensable tool for researchers and clinical laboratories by offering the most reliable solutions in sensitive genetic analysis. With its high sensitivity, inhibitor resistance and user-friendly structure, it shapes the future of dPCR technology and exhibits superior performance compared to its competitors. The advantages offered by Nanowell technology allow for faster genetic research and more precise results.

As Letgen, we enable you to achieve the most sensitive and reliable results in your projects with the Roche #Digital LightCycler® dPCR system. By using this advanced technology device in your molecular biology studies, you can increase quantification precision and data accuracy and add additional value to your projects. With our digital PCR service, we support you at all stages while optimizing your analysis processes. Contact us to use our Roche digital PCR device in your projects and discover more; let's achieve success together!


letgenbio
info@letgenbio.com

Likit Biyopsi ve RNA Calismalarinda Karsilasilan Zorluklar EXTRAClean ile Cozumler

Liquid biopsy is a non-invasive diagnostic method that has revolutionized many fields from cancer to neurological diseases. Liquid biopsy materials obtained from samples such as plasma, serum, urine and cell culture media have great potential for early diagnosis and monitoring of diseases. However, RNA from these samples, especially small extracellular RNA (cfRNA), is present in extremely low concentrations. This can lead to target RNA being missed during RNA isolation. Furthermore, background noise, which inevitably occurs in liquid biopsy samples, complicates the RNA sequencing process and poses serious challenges for analysis and interpretation.

Small RNA Sequencing(Small-seq) Problems Encountered

Small RNA is critical for the study of small RNA molecules, especially microRNAs. However, a number of problems are encountered in this process:

1. Background Noise: Background noise from unwanted sources can mask the true biological signals. This is particularly pronounced in liquid biopsy samples due to the low concentration of RNA. 2. High Proportion of Unmapped Sequences: A significant proportion of the reads obtained during sequencing cannot be accurately mapped on the reference genome. That is, these reads are sequences that cannot be identified where they belong in the genome. This is particularly common in liquid biopsy samples due to low RNA concentration and background noise. Unmapped sequences degrade data quality and make it difficult to detect true biological signals. This prevents researchers from obtaining meaningful and reliable results. 3. Wasted Sequencing Capacity: Some of the reads obtained during sequencing do not carry biologically meaningful information. These "meaningless reads" result in wasted sequencing capacity. For example, if a limited number of reads can be taken in a sequencing run and some of these reads are due to background noise or contamination, this is an inefficient use of sequencing capacity. As a result, additional sequencing runs may be necessary to obtain a sufficient amount of meaningful data. This requires more reagents, time and labor, increasing costs and slowing down the research process.

EXTRAClean Series: A Revolutionary Solution

Norgen Biotek's EXTRAClean series is specifically designed to address these challenges in RNA isolation from liquid biopsy samples and small-seq processes. Unlike conventional methods, EXTRAClean minimizes background noise, allowing for better representation of small RNA species. This significantly reduces unmapped reads during sequencing and increases the mapping rate of microRNAs by up to ten times.

EXTRAClean's What is the Difference?

- Advanced Chemistry and SiC Resin Technology: The EXTRAClean series uses the same high quality SiC resin, while greatly reducing background noise due to its improved chemistry. This ensures high throughput even with samples containing particularly low amounts of RNA.
-
Capture All RNA Sizes: EXTRAClean does not discriminate based on the size of the RNA. It effectively isolates both small and long RNA fragments. This allows for a comprehensive analysis of all RNA species in liquid biopsy samples. - Cost Effectiveness: EXTRAClean significantly reduces sequencing costs. Fewer unmapped reads and higher throughput eliminate the need for additional sequencing runs.

At NPP EXTRAClean Advantages of Using

For sensitive applications such as Next-Generation Sequencing (NGS), using EXTRAClean offers great advantages to researchers:


-
High Sensitivity:
Ensures high quality data even from small amounts of RNA samples.
-
Background
Noise
Minimization:
Clean and noise-free RNA samples provide more accurate and reliable results.- Time and Cost Savings: Fewer sequencing runs are required, speeding up the research process and reducing costs.

Frequently Asked Questions

1. How is EXTRAClean different from its competitors? Why should users chooseEXTRAClean? EXTRAClean offers unparalleled performance in small RNA isolation from liquid biopsy samples. By minimizing background noise, it eliminates the problems seen with other kits. This means higher throughput and lower cost. 2. What are the advantages of using EXTRAClean at NGS? Why should users chooseEXTRAClean? EXTRAClean reduces unmapped reads in the NGS process and increases the mapping rate of microRNAs. This results in cleaner and more meaningful data, while at the same time reducing costs. 3. How is EXTRAClean different from other #Norgen #RNA kits? Has the SiCresin used been changed? EXTRAClean uses the same high-quality SiC resin, but with improved chemistry to reduce background noise. This allows for better results, especially with samples containing low amounts of RNA.

#EXTRAClean sets a new standard in liquid biopsy and small-seq studies. For researchers looking for a cleaner, more efficient and more cost-effective solution, EXTRAClean is an indispensable option.

Letgen As Biotechnology Norgen Biotek 's authorized distributor in Turkey and EXTRAClean series products are available to researchers. EXTRAClean's liquid biopsy and small RNA sequencing You can contact us to experience the superior performance it provides in its work, get detailed information about the products and start the order process.

Letgen In addition to supplying the #EXTRAClean series, we also offer technical support and consultancy services to researchers. In this way, EXTRAClean's You can benefit from its advantages at the highest level and carry out your work more efficiently.

Bakteriyofajlar Antibiyotik Direncinden Tarim ve Gida Guvenligine Biyoteknolojik Cozumler

Antibiotic resistance has become a growing health problem worldwide. Although antibiotics have long been used as effective weapons against bacteria, their excessive and unconscious use causes bacteria to become resistant to these drugs. This creates a serious crisis that threatens human health. Well, scientists who want to find a solution to this problem may have found the solution inspired by nature: Bacteriophages!

Bacteriophages (phages) are viruses specific to bacteria and can be described as natural enemies that wage war against bacteria. Unlike antibiotics, these small but effective viruses target and destroy bacteria in a highly specific way and do not disrupt the natural flora of the organism. Thanks to these unique properties, they can be a promising alternative to antibiotics, especially in the treatment of infections. Their potential to be particularly effective against bacteria that have developed multi-drug resistance makes bacteriophages one of the treatment modalities of the future.

Uses of Bacteriophages

Bacteriophages are not limited to medical treatments. They are also used in a wide range of different disciplines:

- Agriculture Phages : Bacterial diseases are one of the most important causes of crop losses in agriculture. Especially when harmful bacteria infect plants, they can reduce the quality of crops and reduce yields. Chemical pesticides have been used for many years to combat these bacteria, but their environmental impact and bacterial species developing resistance are driving the need for more natural and sustainable solutions in agriculture. Bacteriophages are highly specific against bacterial pathogens in plants, providing an effective solution that protects plants while not harming the environment. For example, phage applications against agricultural pests such as Xanthomonas and Pseudomonas allow farmers to reduce their chemical use and transition to more sustainable farming methods. Scientific studies on the agricultural use of phages show that they can greatly reduce crop losses and at the same time effectively control plant diseases.

-Phagesin Food Safety : Foodborne pathogens are one of the major threats to public health. Bacteria such as Listeria and Salmonella can spread on the surfaces of foods and cause serious health problems. At this point, phages can provide natural protection by targeting harmful bacteria in foods. For example, phages can be used to detect and eliminate pathogens in meat, milk and fresh produce. This not only reduces food waste, but also allows us to offer safer food. - Medical Treatments: Phage therapy is used for resistant infections where antibiotics are ineffective. While they offer an effective solution against targeted bacteria, they do not harm human cells, making them a safe treatment tool. They have been shown to be particularly effective against antibiotic-resistant bacteria such as Clostridium difficile, MRSA (Methicillin Resistant Staphylococcus aureus) and Klebsiella pneumoniae. - Biotechnology and Genetic Engineering: Phages have also become an important tool in the world of genetic engineering and biotechnology. They are used for transferring genetic material into bacteria, manipulating bacteria and even in environmental cleanup applications. This flexibility shows how versatile they are in the world of science.

Having the right tools is crucial in bacteriophage research. Such studies require the right isolation and purification techniques. However, it is quite difficult to find a well-optimized and high-quality kit specifically developed for phage isolation. As Letgen Biotechnology, we recommend Norgen Biotek's Phage DNA Isolation Kit Norgen Biotek's Phage DNA Isolation Kit , which we distribute in Turkey and Azerbaijan, for your phage studies .

- This kit allows you to obtain pure, high-quality phage DNA in less than 45 minutes without the need for hazardous ingredients such as phenol-chloroform or CsCl.- Host DNA, which can be a problem in phage DNA isolation, is not a problem for this kit because the Norgen patented Silico-carbide columns and solutions in the kit have been developed to isolate only phage DNA.- It allows you to isolateboth single-stranded and double-stranded phage DNA.- You can use the DNA you obtain in PCR, qPCR, Restriction Fragment Length Polymorphism(RFLP), Southern Blot, sequencing, cloning studies without the need for extra cleaning processes.- Offering both precision and efficiency in your bacteriophage research, this kit helps you achieve reliable results. To contact us 👇

info@letgenbio.com

https://letgenbio.com/destek-masasi/

IB asilarinin izlenmesi ve varyantlarin tespitini iyilestirin

Infectious Bronchitis Disease (IBV):

Infectious Bronchitis Disease (IBV) is a highly contagious disease that frequently mutates, leading to the emergence of new variants.

IBV vaccination and diagnosis for the most current strategies:

Vaccination based on classical and/or variant strains is widely used in the fight against this disease.

IBV can be diagnosed using 4 main tools: Virus neutralization, HI test, PCR or ELISA.

Each of these tests has its own advantages and limitations.

ADVANTAGES AND LIMITATIONS OF IBV MONITORING TOOLS

Current limitations encountered

ELISA remains the tool of choice for vaccine monitoring. However, kit performance can be limited for the following reasons:

- The evolution of vaccines, especially live vaccines, to include more and more new variants. These variants are either not detected at all or largely undetectable by commercially available kits.

- Difficulty identifying infection in vaccinated herds.

Our Solution Innovative Diagnostics ID Screen® Infectious Bronchitis Indirect 2.0

Our enhanced ELISA kit addresses the issues mentioned above:

- Using a highly conserved recombinant protein, our new kit enables detection of all available variants (4/91, 793B, Qx, It02, var02, var206, BR1, Is02...).

- It can be used to identify challenge caused by classic strains or variants in vaccinated herds.

Please contact us for more detailed information and inquiries. For more information or to place an order -
info@letgenbio.com
can write an e-mail to our address,
-
https://lnkd.in/dKUDN4tm
can schedule an online interview by clicking on our link,
- You can reach us on +90 850 441 2987, - You can contact us via Whatsapp on +90 535 830 05 60.

DNAnin Gizemini Cozmek

Studying DNA is like unraveling the secrets hidden in a mystery book. Each letter, each sequence, forms the basic building blocks of life. However, the methods used to open the pages of this book determine the accuracy of the information you will obtain. Two methods are used. Dye-based methods offer an approach that stains the entire double-stranded DNA and creates an overall glow. Like a flashlight shining on a crowded party, this method illuminates the entire DNA sequence. But here is the problem: Finding the target DNA is like looking for a specific person in a crowd. Because everything is illuminated, it can be difficult to know which sequence is important. This is where the probe-based methods commonly used in qPCR (quantitative PCR) and dPCR (digital PCR), the super tools of molecular biology, were developed to solve this problem. These state-of-the-art probes are like intelligent guides that know exactly where to bind in a DNA sequence. They lock on to a specific target and mark only that sequence, producing a much sharper and more sensitive signal. So probe-based methods allow you to find the answer directly in the complex sea of DNA letters. In other words, while dye-based methods give a general idea, probe-based methods offer the guarantee of getting to the right address. Let's take a closer look at how these probes work and why they are revolutionizing the world of science.



Probes The DNA you are looking for has been found!

It is not easy to specifically recognize and analyze a DNA sequence. That is why special pieces of DNA called probesare used. When the probes find the target sequence, they fit over it like a "lock". But this process is more complex than solving an ordinary jigsaw puzzle. The probes also work like "detectives", marking a specific target in the DNA sequence and showing scientists where it is. Different types of probe can be chosen according to your expectations in the study. Let's get to know the different probe types briefly.



Dual-labeled Probes (TaqMan Probes)

Dual-labeled probes are like a balance where light and darkness meet. These probes have two special molecules at their ends: a fluorescent reporter and aquencher. The fluorescent reporter is a molecule with the potential to emit light; like a flashlight, it "lights up" whether DNA is bound or not. The quencher absorbs the light emitted by the reporter and prevents it from escaping, like a curtain in front of a flashlight. So, under normal conditions, no light can be seen. But during PCR, the magic begins. The probe binds to its target in the DNA and is cleaved by the enzyme polymerase. This cleavage separates the reporter from the quencher and the reporter is freed. At that moment, the reporter molecule begins to emit fluorescence, just as the light from a lantern shines out when the curtain is opened. This glow "lights up", letting scientists know that the target DNA has been found and can be analyzed. Thanks to these properties, double-labeled probes are reliably used in many fields, from diagnosing genetic diseases to detecting viruses. For example, COVID-19 tests use such probes to detect the RNA of the virus.



Double-quencher (Double With extinguisher) Probes Clearer and Sharper Results

Dual-quencher probes are like a special lens that a detective uses to get a sharper and clearer view. They differ from ordinary dual-labeled probes in that they contain two quencher molecules. Normally, a reporter (the molecule that produces fluorescent light) and a quencher (the molecule that absorbs this light) are side by side. The quencher is so close to the reporter that the light from the reporter is absorbed before it is emitted and cannot reach the outside. So, even if the reporter is present, no signal is seen. With dual-quencher probes, however, a second quencher is added to the system, further shortening the distance between the reporter and the quencher. What does this achieve? The shorter the distance, the more unwanted small light that can escape from the reporter is completely absorbed. Thus, unnecessary background light (fluorescence) is largely eliminated. As a result, the signal becomes clearer, stronger and more reliable. This is a great advantage, especially when analyzing long DNA sequences, because the sharpness of the signal makes it easier to identify the right target. Double-quenched probes are like a focusing tool that eliminates blurring when detecting DNA. They are particularly preferred in applications such as the detection of genetic variations (SNPs) and the analysis of rare mutations.



MGB Probes: Short, Sharp and Strong

Molecules called Minor Groove Binders (MGB) grip the DNA by holding tightly to the small grooves on its surface. MGB grips the tiny folds of the DNA like a key fitting snugly into a lock, allowing the probe to bind to the DNA much more strongly. This tight grip increases the melting temperature (Tm) of the probe, meaning it is harder for the probe to detach from the DNA sequence.

What does this mean? Normally, for a probe to bind to DNA, the sequences need to be long so that the binding is strong. But MGB probes bind so strongly to DNA that the sequence doesn't need to be long. Even short sequences become very stable and perfectly recognize the target sequence. In short, thanks to MGB probes, scientists can confidently detect the target DNA sequence with shorter and more precise probes.

This is a great advantage, especially in complex systems such as multiplex PCR. Multiplex PCR is a process where multiple DNA sequences are analyzed simultaneously and accuracy is vital. MGB probes provide accurate and reliable results even when analyzing complex sequences because they clearly recognize the target sequence. Therefore, MGB probes are frequently preferred especially for amplification of regions with high GC content.




LNA Probes: To Solve the Toughest Mysteries in DNA

Some DNA sequences are more complex than others and detecting small changes in these sequences is not always easy. In particular, genetic variations- when even a single letter in DNA is different (these changes are called polymorphisms) - are a challenge, like finding the missing piece of a puzzle. For such challenges, scientists use special probes called Locked Nucleic Acid(LNA). The power of LNA probes comes from the fact that they are different and more robust than ordinary DNA building blocks. While normal DNA forms flexible and loose bonds, LNA building blocks form tight and stable bonds, like a locked door. This structure allows LNA probes to attach much more strongly to the DNA sequence. Just like a strong magnet sticks firmly to a metal surface, LNA probes grip the target DNA tightly. What does this achieve? LNA probes can detect even very small changes in the DNA sequence. For example, if only a single base (one of the letters A, T, C, G) is different in a sequence, the LNA probe will pick up this difference and signal correctly. This makes LNA probes ideal for highly sensitive and accurate applications, such as the detection of genetic diseases. LNA probes work like a detective, capturing even the finest details in DNA, allowing us to solve difficult targets with confidence. They are frequently used in applications such as multiplex PCR, detection of single base polymorphisms (SNPs), microRNA analysis and gene expression studies. LNA probes also have the potential to be used in antisense technology studies.



Molecular Beacons: The Power of Hairpin Structure

Molecular beacons get their name from their unique structure; they curl like a hairpin. These special probes are like a sensitive detector that tracks DNA and only activates when it finds its target. Normally, molecular beacons form a closed structure in the shape of a hairpin. At the ends of this closed structure are a fluorescent reporter and a quencher. The reporter molecule wants to emit light, but the quencher is so close to it that it absorbs it immediately. Therefore, when the beacon is off, fluorescence cannot be seen through the quencher. When the beacon is fully aligned to the target, the hairpin structure opens and the reporter and quencher move away from each other. At that moment, the reporter molecule is released and starts to emit fluorescent light. This signal indicates that the target DNA has been successfully detected. The most important feature of molecular beacons is that they are extremely sensitive. They can even detect a change in a single DNA base, such as the letter G instead of A. This is a huge advantage, especially in genetic analysis, where even very small differences are important. Beacons wait until they find the right target, and when they do, they signal just like a light bulb going on. They are widely used in areas such as gene expression analysis, pathogen detection and genetic diagnosis.



Tm(Melting Temperature) Enhancing Modifications: DNA Specific Tuning

The secret to success in PCR is to get the DNA to open at the right temperature. Tm (melting temperature) is the temperature at which the double helix structure of DNA dissolves and becomes a single helix. In other words, it is the temperature at which the two DNA strands are separated. The Tm value affects how tightly the primer binds to the target DNA. If the Tm value of the primer is too low, the primer will not bind strongly enough to the target DNA, which can lead to false results. Therefore, depending on the needs of your study, it is sometimes necessary to increase the Tm value to increase the binding strength of the primer to the target DNA. This is where "Tm-enhancing modifications" can be a great help. These modifications aim to increase the Tm value by adding special chemical groups to the structure of the primer. For example, modifications such as propynyl-dC(pdC) and propynyl-dU(pdU) strengthen the bonds between DNA and primer. These modifications increase hydrogen bonds between DNA molecules, allowing the double helix structure to unwind at higher temperatures. Just as a magnet sticks more firmly to a stronger magnet, modified primers bind more firmly to the target DNA. pdC increases the Tm value by about 2.8°C, while pdU increases it by 1.7°C.



As for the benefits of Tm-enhancing modifications;

- It enables primers to bind more specifically and strongly to the target DNA, reducing the risk of false positive or false negative results.

- Increases the sensitivity of PCR by enabling detection of even low amounts of target DNA.

- It gives better results in challenging PCR applications, for example when amplifying regions with high GC content or when multiple targets are amplified simultaneously, such as multiplex PCR.

Conclusion: Decoding DNA

Molecular biology is the process of decoding DNA, and probes are scientists' most reliable assistant in this process. With technologies such as qPCR and dPCR, these probes reveal genetic information in the most accurate and precise way. Advanced probe types, especially innovations such as LNA and MGB, ensure success even with complex and difficult targets. Therefore, analyzing DNA has become more precise, more reliable and faster.

In conclusion, the probes used in qPCR and dPCR technologies are the most powerful tools at our disposal to unlock the secrets of DNA. Each probe type, with its unique advantages, opens new doors for researchers, clinicians and the entire scientific world. These molecular keys are revolutionizing science by enabling us to understand the codes of life.

Probe By : Letgen Biotechnology & Microsynth

In our mission to provide the best service to the scientific community, Letgen Biotechnology has a strong collaboration with Microsynth, one of Europe's leading nucleic acid synthesis and analysis companies. Thanks to this partnership, we are able to offer researchers the highest quality probes at competitive prices.

Why? Microsynth Should You Choose Probes?

Microsynth probes have a number of advantages to ensure you get the most accurate and reliable results for your genetic research:

- Fast Production Times: You can have your probes in just 3-7 working days. We understand how valuable time is and offer fast delivery to ensure your research goes smoothly. - Customizable Coupling Affinity: With MGB, LNA and other Tm enhancers, you can customize the binding affinity according to your project's requirements, or even use multiple enhancers together for optimal results. Just like a tailor tailors an outfit, you can design the probes specifically for your project. - Wide Fluorescent Reporter-Extinguisher Options: We offer a wide range of options from which you can choose the combination that best suits your experimental needs. You can optimize your experiments by choosing between fluorescent reporters and quenchers in different colors. - Expert Design Support: With Microsynth&Letgen's professional probe design service, you can ensure that your experiments are on the right track from the very beginning. Our expert teams analyze the requirements of your project and provide you with the most suitable probe designs.
-
Certified Quality:
With our EN ISO 13485:2016 certified manufacturing process, we offer the assurance of using probes manufactured to the highest quality standards. Quality is the cornerstone of your research and Microsynth gives you full assurance. - Comprehensive Services: By entrusting your qPCR and digital PCR assay development, validation, manufacturing and testing to Microsynth&Letgen, you can have a seamless experience. We manage the entire process for you from start to finish, so you can focus on your research.

Presented in collaboration with Letgen Biotechnology and Microsynth, these high quality probes will accelerate your scientific discoveries and open new horizons in your research. With our competitive prices, you can get the best quality without breaking your budget. Letgen Biotechnology and Microsynth are always with you on your path to scientific success.


MikroRNAlarin Sessiz Devrimi

Seemingly small in size but big in impact, miRNAs are quietly revolutionizing the biological world. These molecules, which are at the root of many diseases by controlling the expression of genes, are opening the doors to new treatment and diagnosis methods in the medical world. Perhaps in the near future, we will be able to fight many diseases much more effectively thanks to microRNA-based therapies!

Now think about it, isn't it exciting to know how deeply such a small molecule can affect our cells and our health? If you say, "It's not enough to just know, I want to study it too",
Letgen
Biotechnology
we encourage you to take a look at our premium quality brands, where you can discover microRNA for yourself.

microRNA: The Hidden Rulers of Cells and New Hope for Fighting Disease

It is well known that structures such as DNA and mRNA, which carry genetic information, are behind many of the complex events that take place in our cells. However, microRNA (miRNA), one of the hidden heroes of biology, has a key role in regulating all these processes! miRNAs, which are not talked about much but accomplish great things, almost secretly manage the control center of the cell. Thanks to Victor Ambros and Gary Ruvkun, who received the 2024 Nobel Prize for their work on microRNAs, interest in microRNAs has increased. Let's get to know these small but effective molecules briefly!

microRNA What is it?

Briefly defined, microRNAs (miRNAs) are small RNA molecules, approximately 22 nucleotides in length, that are located inside the cell. They do not code for proteins but indirectly control protein production. How? miRNAs bind to mRNAs carrying genetic messages and prevent them from doing their job. In a way, they determine when genes are active and how much protein is produced. It is hard not to be surprised to learn that they have such a say in the functioning of the cell!

microRNA What does it do?

Here's the kicker: miRNAs bind to mRNA and either degrade and destroy it or stop protein synthesis. This is a critical step to control gene expression and maintain balance in the cell. They even regulate many biological processes by influencing the behavior of the cell. These processes range from cell division to death.

In other words, these small molecules act like a "control panel" inside the cell, regulating which genes are "on" or "off". This is exactly why miRNAs are referred to as "silent rulers" in the biological world.

microRNA and Diseases: The Hidden Link in the World of Health

The gene regulatory role of microRNAs places them at the center of diseases. In particular, miRNAs have been strongly associated with many diseases such as cancer, heart disease, neurodegenerative disorders (e.g. Alzheimer's) and metabolic diseases. Here are a few striking examples:


-
Cancer:
miRNAs can often be either overactive or completely repressed in cancerous cells. Some miRNAs function as tumor suppressors, while others may act as oncogenes (cancer-forming). Therefore, analyzing miRNA profiles becomes crucial in diagnosing cancer and monitoring response to treatment.
-
Heart Disease:
Certain miRNAs play important roles in conditions such as healing damage after a heart attack. Events such as the growth or death of heart muscle cells are complex processes governed by miRNAs. - Neurological Diseases: In diseases such as Alzheimer's and Parkinson's, miRNAs can affect the function of brain cells. Research shows that some miRNAs play a role in maintaining or disrupting the health of nerve cells.

miRNA in the Future: New Horizons in Treatment and Diagnosis

This controlling role of microRNAs in cells makes them a powerful tool in the medical field. miRNA-based therapies are promising in the prevention or treatment of many diseases. For example, studies on suppressing or activating target genes in cancer treatment with the help of miRNAs continue rapidly.

- MicroRNA Inhibitors: If a miRNA is overactive and causes disease, inhibitors can be developed to stop this miRNA. This prevents the suppression of disease-causing genes.
-
miRNA
Supplements:
On the other hand, the balance in the cell can be restored by replacing missing or inadequately functioning miRNAs with synthetic miRNAs produced in the laboratory.

miRNAs can also be used as biomarkers in complex diseases such as cancer. Measuring the levels of specific miRNAs in blood tests has great potential for early diagnosis and monitoring disease progression.

miRNA and Personalized Medicine

In the field of personalized medicine, which we have heard of frequently in recent years, miRNAs are in the lead role! By analyzing the genetic and miRNA profiles of patients, it becomes possible to tailor treatment options to the individual. Especially in cancer treatment, more targeted and effective treatments are expected to be developed thanks to these personalized approaches.

Mikro Dunyada Tasarim Zamani

It's time to design high quality and reliable primers and probe designs for your molecular biology studies!

Even if you don't know how to design,
Microsynth
AG
&
Letgen
Biotechnology
we open the doors of the micro world to you.

If you have limited knowledge and work you want to do, you can realize your work in a short time thanks to Microsynth's and Letgenbio's expert team!

Experience hassle-free primer/probe design and synthesis with a comprehensive product range, fast delivery and expert support from Microsynth, a Swiss-based company.

In Microsynth's high-capacity synthesis facilities in Switzerland, your orders are prepared by hand in fully automated systems and delivered to you as soon as possible with the lowest carbon emissions under the assurance of Letgen.

Microsynth offers oligonucleotides to suit your needs with a wide range of modifications and purification options. DNA & RNA Oligonucleotides, Locked Nucleic Acid (LNA), MGB, Internal Quencher (IQ-500) modifications and more.

Get ready to take your research to the next level with the ease and assurance of working with Microsynth and Letgen!

For detailed information and order:

oligo@letgenbio.com