JavaScript is currently not supported/disabled by this browser. Please enable JavaScript for full functionality.
Loding Loading ....

Solutions for Methylation Library Preparation

Published On 01/23/2025 11:23 AM


Solutions for Methyl-seq DNA Library Preparation


DNA methylation—a better tumor early screening marker

Cancer is one of the leading causes of morbidity and death in the world, and about 1 out of every 6 deaths worldwide is due to cancer. According to the "2022 National Cancer Data Report", there are 4.064 million new cases of cancer in the country, and almost 8 people suffer from cancer every minute. Combined with the latest 2020 global cancer burden data previously released by the WHO.

The development of cancer is a multi-stage slow process, which generally takes 10 to 15 years from normal to precancerous lesions. Early detection, early intervention, and early treatment are currently the best means of cancer prevention and treatment. At the same time, early detection, early intervention, and early treatment can also greatly improve the effective treatment and survival of patients.

Studies have found that the occurrence of cancer is accompanied by changes in DNA methylation patterns, including retroelements, centromeres, and hypomethylation of proto-oncogenes. Changes in methylation patterns play a key role in the occurrence and development of tumors, and exist almost throughout the development of tumors including precancerous lesions. Therefore, more and more studies will use DNA methylation detection as a marker for early screening of cancer.

At Biohippo, we partner with Yeasen Biotechnologies, a leading provider of molecular diagnostics products, to offer the research tools necessary for detecting DNA methylation.

 

NO.1 DNA Methylation Bisulfite Kit—— Cat No. BHN20800024


The Hieff Superfast DNA Methylation Bisulfite Kit (Column-based) rapidly converts unmethylated cytosines in DNA samples to uracil, while leaving methylated cytosines unchanged. During high-temperature bisulfite treatment, double-stranded DNA denatures into single strands. In the presence of HSO3-, cytosine residues undergo deamination and are converted into uracil, with methylated cytosines remaining unaltered. In subsequent PCR amplification, uracil is replaced by thymine (T). The conversion process takes only 5 minutes, accommodating DNA input ranging from 100 pg to 2 ug, and achieves a conversion efficiency of >=99% for unmethylated cytosines. The converted DNA is suitable for downstream applications such as PCR amplification and NGS sequencing.


Product Highlights:

- Low input: can meet the conversion of 500 pg-2 μg samples
- High conversion efficiency: conversion rate ≥ 99%
- Easy to operate: conversion can be completed within 3 hours


Figure 2. conversion rate of λDNA C in gDNA of 293T cells with different inputs

   

NO.3 ssDNA Assay Kit——12645ES

 Product Highlights:

Good linear range: R2>0.99;
High sensitivity and wide application range: quantification of 1~200 ng samples;
Strong tolerance: good tolerance to conventional pollutants such as proteins, salts, detergents, etc.  Product orderingProduct

CAT

Product application

MolPure® Magnetic Cell-Free DNA Kit 

18381ES

cfDNA extraction

Hieff superfast DNA Methylation Bisulfite Kit

12225ES

Methylation conversion

ssDNA Assay Kit

12645ES

Single stranded DNA (ssDNA) quantification

1×dsDNA HSAssay Kit

12642ES

Double stranded DNA (dsDNA) quantification