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IHC-P analysis of human breast carcinoma tissue using GTX22851 DNMT3B antibody. Right : Primary antibody Left : Negative control without primary antibody Antigen retrieval : 10mM sodium citrate (pH 6.0) microwaved for 8-15 min Dilution : 1:500
IHC-P analysis of human breast carcinoma tissue using GTX22851 DNMT3B antibody. Right : Primary antibody Left : Negative control without primary antibody Antigen retrieval : 10mM sodium citrate (pH 6.0) microwaved for 8-15 min Dilution : 1:500
IHC-P analysis of human breast carcinoma tissue using GTX22851 DNMT3B antibody. Right : Primary antibody Left : Negative control without primary antibody Antigen retrieval : 10mM sodium citrate (pH 6.0) microwaved for 8-15 min Dilution : 1:500

DNMT3B antibody

GTX22851
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman, Mouse
TargetDnmt3b
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Overview

  • Supplier
    GeneTex
  • Product Name
    DNMT3B antibody
  • Delivery Days Customer
    9
  • Antibody Specificity
    This antibody has been used to detect both recombinant and endogenous DNMT3b and recombinant DNMT3a.
  • Application Supplier Note
    WB: 2.0 microg/ml. IHC-P: 1:100-1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID13436
  • Target name
    Dnmt3b
  • Target description
    DNA methyltransferase 3B
  • Target synonyms
    DNA (cytosine-5)-methyltransferase 3B; DNA methyltransferase MmuIIIB; DNA MTase MmuIIIB; MmuIIIB
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDO88509
  • Protein Name
    DNA (cytosine-5)-methyltransferase 3B
  • Scientific Description
    This is one of two related genes encoding de novo DNA methyltransferases, which are responsible for the establishment of DNA methylation patterns in embryos. Loss of function of this gene results in severe developmental defects and loss of viability. Mutation of the related gene in humans causes immunodeficiency-centromeric instability-facial anomalies (ICF) syndrome. There is a pseudogene for this gene located adjacent to this gene in the same region of chromosome 2. Alternatively spliced transcript variants encoding multiple isoforms have been observed. [provided by RefSeq, Nov 2012]
  • Reactivity
    Human, Mouse
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • Protein phosphatase 2A inactivation induces microsatellite instability, neoantigen production and immune response. Yen YT et al., 2021 Dec 15, Nat Commun
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