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DNA/RNA Methylation Reagents for Epigenetic Mapping and Quantification

 

DNA/RNA Methylation covers the reagents used to detect, map, and quantify methylation marks in genomic DNA and RNA, including bisulfite conversion reagents for single-base-resolution cytosine methylation analysis, enzymatic conversion tools as a less damaging alternative, antibody-based MeDIP and 5-hmC detection kits, and RNA methylation assays targeting marks such as m6A. These tools complement the synthetic methylated controls available through modified dNTPs in the sibling subcategory. Academic and core laboratories mapping methylation patterns across the genome or at specific loci can benefit from guidance when selecting the most appropriate detection and analysis method for their experimental goals.

Explore available DNA and RNA methylation reagents or request a quotation by contacting customerservice@mbpinc.net. Our team can help identify the appropriate conversion, enrichment, detection, and analysis tools for your epigenetics research workflow.

DNA/RNA Methylation

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2X Test Reaction PreMix
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2X Test Reaction-Lite PreMix
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5-mC Coating Buffer
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5-mC DNA ELISA Kit (2 x 96 Preps.)
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5-mC DNA ELISA Kit (96 Preps.)
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USD597.17
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Anti-5-Hydroxymethylcytosine Polyclonal Antibody
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USD140.98 - USD780.71
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USD100.70 - USD557.65
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Anti-5-Methylcytosine (Clone 7D21) (0.5 µg/µl)
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USD77.14 - USD751.45
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Bisulfite Converted Universal Methylated Human DNA Standard
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USD194.18
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CT Conversion Reagent
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DNA Controls
D5325-5-1
DNA Controls
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DNA Denaturing Buffer (1 ml)
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E. coli Non-Methylated Genomic DNA (5 µg/20 µl)
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USD159.60
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What is DNA/RNA Methylation as a reagent category?

 

DNA/RNA Methylation covers the detection and quantification side of epigenetics: the reagents used to identify which cytosines in a DNA sample are methylated, distinguish 5-methylcytosine from 5-hydroxymethylcytosine, and detect RNA methylation marks like N6-methyladenosine (m6A). Methods range from bisulfite conversion, the historically standard approach for single-base-resolution cytosine methylation mapping, to enzymatic conversion as a less damaging alternative, to antibody-based immunoprecipitation for broad-scale enrichment of methylated DNA regions, to direct ELISA-based quantification of global methylation levels.

 

What you will find:

 

 

How to choose DNA/RNA methylation analysis reagents

 

Choose bisulfite conversion for single-base-resolution cytosine methylation mapping

Bisulfite conversion converts unmethylated cytosines to uracil while leaving 5-methylcytosine largely unchanged under standard conditions, and after amplification and sequencing, the resulting base-pair difference reveals exactly which cytosines were methylated, making it the approach for single-base-resolution mapping but one that introduces significant DNA damage and degradation.

Consider enzymatic conversion as a less damaging alternative to bisulfite treatment

Enzymatic conversion methods achieve the same cytosine-to-uracil discrimination as bisulfite but through enzymatic rather than harsh chemical reactions, minimizing DNA damage and producing higher-quality libraries from fewer sequencing reads, at potentially higher reagent cost.

Use antibody-based MeDIP for broad methylation enrichment without locus-by-locus resolution

Methylated DNA immunoprecipitation uses an antibody against 5-methylcytosine or 5-hydroxymethylcytosine to enrich methylated DNA regions from a fragmented sample, providing genome-wide enrichment data without the single-base resolution of bisulfite sequencing.

Confirm your method can distinguish 5-mC from 5-hmC if that difference matters for your study

Standard bisulfite conversion cannot reliably distinguish 5-methylcytosine from 5-hydroxymethylcytosine, since both resist bisulfite-mediated deamination under standard conditions, so confirming whether your study requires that distinction helps determine whether a specialized additional step is needed.

Choose ELISA-based kits for rapid, global methylation quantification without sequencing

A 5-methylcytosine ELISA kit provides a rapid, quantitative readout of the global level of DNA methylation in a sample without requiring bisulfite conversion or sequencing, useful for broad-level comparisons across multiple conditions or samples when single-base resolution isn't needed.

 

Specifications context

 

Bisulfite sequencing is widely regarded as the gold standard for DNA methylation analysis due to its single-base resolution, but it introduces significant technical challenges for amplification and next-generation sequencing library preparation due to DNA degradation, reduced genome complexity, and alignment complexity from the cytosine-to-uracil base conversion. As of 2026, enzymatic conversion is increasingly recommended over bisulfite conversion for methylation analysis specifically because it minimizes these DNA damage and quality issues, enabling improved preservation and detection of cytosine methylation marks from fewer sequencing reads with no change to downstream analysis pipelines.

Contact the expert team at Molecular Biology Products Inc. (MBP) today and get reliable DNA/RNA methylation kits for your lab.

FAQ

Bisulfite conversion uses sodium bisulfite to chemically deaminate unmethylated cytosines into uracil while leaving 5-methylcytosine intact, so after PCR amplification and sequencing, unmethylated cytosines read as thymine while methylated cytosines remain as cytosine, revealing methylation at single-base resolution. It's considered a gold standard because it provides this precise, locus-by-locus view of methylation status, though it introduces significant DNA damage and degradation that can complicate downstream analysis.
Enzymatic conversion achieves the same cytosine discrimination as bisulfite but through enzymatic reactions rather than harsh chemical treatment, minimizing DNA damage and fragmentation and producing higher-quality sequencing libraries from fewer total sequencing reads, while still being compatible with standard downstream bioinformatic analysis pipelines. This quality improvement, without needing to change downstream analysis, is why many labs are making the switch from bisulfite to enzymatic conversion.
Standard bisulfite conversion cannot reliably distinguish 5-methylcytosine from 5-hydroxymethylcytosine because both modifications resist bisulfite-mediated deamination under standard conditions and both read as cytosine after sequencing. Specialized additional steps or alternative methods, such as oxidative bisulfite sequencing or specific enzymatic approaches, are needed when distinguishing between these two marks is important for your specific research question.
Methylated DNA immunoprecipitation is a good choice when you want genome-wide enrichment data without needing the single-base resolution that bisulfite or enzymatic conversion provides, or when you're working with a sample type or experimental design where broad regional enrichment is more informative than precise per-cytosine status. MeDIP also avoids the harsh chemical treatment and DNA damage that bisulfite conversion introduces.
A 5-methylcytosine ELISA kit provides a quantitative measure of the global percentage of DNA methylation across a sample without needing bisulfite conversion or sequencing, making it a rapid, accessible option when broad-level comparison of total methylation across multiple samples or conditions is the goal. It's not suitable when single-base or regional resolution is needed, but for global quantification or high-throughput screening across many samples, it's a practical alternative to sequencing-based approaches.
Methylation-sensitive qPCR uses bisulfite or enzymatic conversion as an upstream step to discriminate methylated from unmethylated cytosines at a specific locus, then uses qPCR with primers specifically designed for the converted sequence to quantify methylation at that targeted region. This approach is well suited to validating a specific locus identified through discovery methods like WGBS or MeDIP, rather than discovering new methylated regions.
N6-methyladenosine (m6A) is the most widely studied RNA methylation mark, present on mRNA and other RNA species, and can be detected via antibody-based immunoprecipitation (m6A-RIP-seq) or ELISA-based global quantification kits, similar in approach to the antibody and ELISA methods used for DNA methylation. Some epigenetics methylation catalogs, including this one, group RNA methylation detection tools alongside DNA methylation reagents given their shared focus on methylation biology.
Yes, MBP offers academic and bulk pricing across bisulfite conversion reagents, enzymatic methylation analysis kits, antibody-based detection tools, and RNA methylation assays, with specialist support for method selection. Orders ship from MBP's US office in Houston, Texas, with stock available in both USD and CAD.
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