Purified anti-DNMT3B Antibody anti-DNMT3B - W15184A,BioLegend,695202

Based on sequence homology, this antibody should recognize isoforms 1-6 of DNMT3B with MW ranging from 81kD to 96kD. However, according to the immunogen sequence, there is a possibility that the antibody might not recognize isoforms 7 and 8.This clone is not recommended for ChIP (Chromatin Immunoprecipitation) assays (as determined by in-house testing).

Host

Mouse

Reactivity

Human

Application

WB - Quality tested

Platform ID

BAB390835511

BioLegend

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Contact

Tel: 1-858-455-9588
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Product Specifications
Scientific Background

Specifications

NamePurified anti-DNMT3B Antibody anti-DNMT3B - W15184A
Cat. No.695202
HostMouse
RRIDAB_2650802 (BioLegend Cat. No. 695202)
IsotypeMouse IgG1, κ
ReactivityHuman
ApplicationWB - Quality tested
ClonalityMonoclonal
Clone NumberW15184A
Concentration0.5 mg/ml
TargetDNMT3B
ImmunogenPartial human DNMT3B recombinant protein (1-355 a.a.) expressed inE. coli.
PurityThe antibody was purified by affinity chromatography.
FormulationPhosphate-buffered solution, pH 7.2, containing 0.09% sodium azide.
StorageThe antibody solution should be stored undiluted between 2°C and 8°C.
Regulatory StatusResearch Use Only

Scientific Background

DNA (cytosine-5-)-methyltransferase 3 beta, also known as DNMT3B, is an enzyme responsible for establishing DNA methylation patterns. DNA methyltransferases in mammals are comprised of four family members: DNMT1, DNMT3A, DNMT3B, and DNMT3L. DNMT3B, as well as DNMT3A, act as de novo methyltransferases that modify unmethylated DNA, whereas DNMT1 functions in the maintenance of DNA methylation pattern. DNA methylation is a covalent modification that involves the transfer of a methyl group from S-adenosylmethionine to the 5’ cytosine residue at CpG dinucleotides of the genomic DNA. CpG methylation is usually associated with transcriptional repression and is required for embryonic development, imprinting, genomic stability, and X-chromosome inactivation. Defects in DNMT3B gene in human cause the immunodeficiency-centromeric instability-facial anomalies (ICF) syndrome.

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