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AB117127

Fast Bisulfite Conversion Kit

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(3 Publications)

Fast DNA modification Kit (ab117127) allows DNA denaturation and bisulfite conversion to be processed at the same time so the complete procedure can be performed in only 30 minutes.
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Functional Studies - Fast Bisulfite Conversion Kit (AB117127)
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Supplier Data

Functional Studies - Fast Bisulfite Conversion Kit (AB117127)

Effective DNA Protection : Fully methylated human genomic DNA at various amounts (0.2 ng-200 ng) were converted using the ab117127. 1 µl of 20 µl eluate was used for real time qPCR and a pair of primers was used to amplify converted DNA. As little as 0.2 ng DNA is sufficient for bisulfite conversion using the ab117127. A : real time PCR; B : starting DNA amount-CT value curve.

Functional Studies - Fast Bisulfite Conversion Kit (AB117127)
  • FuncS

Supplier Data

Functional Studies - Fast Bisulfite Conversion Kit (AB117127)

Complete Cytosine Conversion : 200 ng of genomic DNA isolated from 3 cancer cell lines was treated with ab117127. Next, the unconverted and converted DNA in each treated sample were determined using unconverted DNA-specific and converted DNA-specific primers (ß-actin, 110 bps), respectively. A : real time PCR; B : end-point PCR. The ab117127 treated DNA was completely converted, and no unconverted DNA in the treated samples was determined after 45 cycles.

Key facts

Assay time

30m

Product details

Fast DNA modification Kit (ab117127) allows DNA denaturation and bisulfite conversion to be processed at the same time so the complete procedure can be performed in only **30 minutes**. Furthermore, it prevents more than 90% of DNA loss, completely converting unmethylated cytosine into uracil.Traditional methods involve a separate denaturation step followed by a subsequent sodium bisulfite DNA conversion step - but with ab117127, DNA denaturation status is concurrently sustained throughout the entire bisulfite DNA conversion process. ab117127 is suitable for MS-PCR, real time MS-PCR, bisulfite sequencing, pyrosequencing and methylation microarray.DNA methylation is a covalent modification of the cytosine ring at the 5' position of a CpG dinucleotide which leads to epigenetic inactivation of genes when found in 5'-CpG-3'dinucleotides within promoters or in the first exon of genes. It is well demonstrated that DNA methylation plays an important role in the regulation of gene expression, tumorigenesis, and other genetic and epigenetic diseases.Most methods for DNA methylation detection require a prior bisulfite-based DNA modification. *Bisulfite-based DNA modification* is used to discrimate between cytosine and methylated cytosine, in which DNA is treated with bisulfite salt to convert cytosine residues to uracil in a single-stranded DNA, while methylated cytosine remains the same. Not sure if this is the right kit for you? Check out our for more information.

What's included?

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Properties and storage information

Shipped at conditions
Ambient - Cannot Ship with Ice
Appropriate short-term storage conditions
Ambient
Appropriate long-term storage conditions
Ambient
Storage information
Ambient

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

Publications (3)

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Genome research 32:2079-2091 PubMed36332968

2022

Methyl-SNP-seq reveals dual readouts of methylome and variome at molecule resolution while enabling target enrichment.

Applications

Unspecified application

Species

Unspecified reactive species

Bo Yan,Duan Wang,Romualdas Vaisvila,Zhiyi Sun,Laurence Ettwiller

Journal for immunotherapy of cancer 9: PubMed34413165

2021

Hypermethylation of CD19 promoter enables antigen-negative escape to CART-19 in vivo and in vitro.

Applications

Unspecified application

Species

Unspecified reactive species

Aneta Ledererova,Lenka Dostalova,Veronika Kozlova,Helena Peschelova,Adriana Ladungova,Martin Culen,Tomas Loja,Jan Verner,Sarka Pospisilova,Michal Smida,Veronika Mancikova

PloS one 13:e0199091 PubMed29902267

2018

Evaluation of bisulfite kits for DNA methylation profiling in terms of DNA fragmentation and DNA recovery using digital PCR.

Applications

Unspecified application

Species

Unspecified reactive species

Sam Kint,Ward De Spiegelaere,Jonas De Kesel,Linos Vandekerckhove,Wim Van Criekinge
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