Unlock the Epigenetic Secrets of DNA Demethylation
Discover how 5fC, a pivotal intermediate in DNA demethylation, regulates gene expression and plays a crucial role in cellular reprogramming. Our advanced detection services provide high-resolution, genome-wide profiling of 5fC, empowering your research in epigenetics.
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5-Formylcytosine (5fC) is a critical epigenetic mark involved in gene regulation and cellular identity. It is central to understanding the underlying mechanisms in cancer, neurodegeneration, and development. Traditional 5fC detection methods often lack the necessary sensitivity and resolution for genomic-scale analysis. At CD Genomics, we provide advanced 5fC sequencing that delivers single-base resolution profiling, enabling precise mapping of 5fC across various biological contexts—from tumorigenesis to neurodegeneration and stem cell differentiation.
Our technologies, including fC-Seal and fCAB-Seq, offer high sensitivity and accurate genome-wide analysis, even from low-abundance samples. These technologies allow you to track dynamic changes in 5fC and link them directly to gene expression in your research.
At CD Genomics, we understand that accurate and reliable 5fC detection is essential for your research. To support this, we utilize advanced technologies that ensure precision, sensitivity, and resolution, enabling you to gain deeper insights into 5fC's role in epigenetics.
What Makes It Unique:
The fC-Seal method is a highly specialized approach designed to provide targeted detection of 5fC without the complexity of antibody-based systems. This method chemically reduces 5fC to 5-hydroxymethylcytosine (5hmC), then tags it using a specific enzyme to enrich the 5fC sites for further sequencing. This technique eliminates the potential for cross-reactivity, providing precise and reliable results.
Why Choose fC-Seal:
This method is particularly suited for projects requiring high sensitivity and accuracy at every step, from initial detection to final analysis.
What Makes It Unique:
The fCAB-Seq method stands out by combining the power of bisulfite sequencing with a unique chemical stabilization process. During bisulfite treatment, 5fC could normally convert to thymine, but our approach stabilizes 5fC, ensuring it can be accurately detected through sequencing. This means you can trust that no valuable data will be lost, even when working with large datasets.
Why Choose fCAB-Seq:
With this method, you can confidently explore the intricacies of 5fC in your research, whether you're focusing on a few key genes or conducting large-scale studies.
Both of these methods provide the tools needed to accurately map, quantify, and understand the dynamic role of 5fC in epigenetic regulation. Whether working with limited sample sizes or large genomic datasets, our technologies ensure you get the most reliable, actionable insights.
Understanding 5fC's genomic role is critical for deciphering complex biological processes. At CD Genomics, our 5fC detection services enable research across diverse fields—from cancer to neurodegenerative diseases—by delivering insights into underlying molecular mechanisms.
5fC plays a pivotal role in regulating genes linked to tumor development. Our services help map 5fC in cancer cells, revealing how it drives gene expression changes associated with tumorigenesis and progression. Key areas of support include:
Altered 5fC patterns are linked to conditions like Alzheimer's and Parkinson's. Our detection methods enable researchers to explore how 5fC influences gene regulation changes that contribute to neurodegeneration. Applications include:
5fC is essential for maintaining stem cell pluripotency and guiding differentiation. Our services support studies on how 5fC modifications shape stem cell fate and developmental processes. Key research areas include:
5fC participates in epigenetic reprogramming, a process tied to age-related cellular changes. Our services help researchers investigate how 5fC modifications drive age-related gene expression and functional alterations. Applications include:
Once your 5fC detection analysis is complete, we provide a detailed, easy-to-understand report that highlights the key findings. Our goal is to deliver actionable insights that can drive your research forward, with clear visualizations, bioinformatics analysis and expert analysis.
With our detailed reports, you can confidently move forward in your research, knowing you have clear, reliable, and interpretable data to guide your next steps.
When it comes to 5fC detection, CD Genomics offers the precision, reliability, and expertise you need to support your research. Here's why we are the right choice for your 5fC analysis:
We employ state-of-the-art technologies, including fC-Seal and fCAB-Seq, to provide precise and high-resolution 5fC mapping. Our methods ensure that you get the most accurate data for exploring gene regulation, epigenetic reprogramming, and other biological mechanisms.
At CD Genomics, we recognize that every research project is unique. That's why we offer tailored services to suit your specific study requirements. Whether working with smaller sample sets or large-scale genomic analysis, we adjust our approach to provide you with the best results.
We are committed to supporting your research with expert advice and guidance throughout the entire process. From initial consultations to post-analysis discussions, our team is always available to ensure your study's success.
Our services go beyond just delivering raw data. We assist in interpreting your results, offering in-depth analysis and insights that help you gain a better understanding of the biological significance of 5fC modifications in your research. We also provide ongoing support to help you integrate these insights into your work.
We understand the importance of timely results in research. Our efficient process is designed to deliver high-quality data without delays. You can rely on us for consistent, dependable results every time.
We prioritize your needs and are dedicated to ensuring you receive the highest level of service. We communicate clearly at every stage of the project and are flexible in adapting to any changing research requirements. Our goal is to support your work in every way possible.

| Criteria | Details |
|---|---|
| Sample Types | Genomic DNA from tissues, cells, or blood (fresh or frozen) |
| DNA Quality | DNA concentration: Minimum 1 µg per sample; Purity: A260/A280 ratio between 1.8-2.0 |
| Shipping Instructions | Store samples at -20°C or -80°C and ship on dry ice |
| Sample Preparation Tips | Avoid contamination from phenol, salts, or other chemicals; ensure proper extraction |
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