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DNMT3B antibody (AA 1-150)

This Mouse Monoclonal antibody specifically detects DNMT3B in ELISA, FACS and ICC. It exhibits reactivity toward Human.
Catalog No. ABIN5542517

Quick Overview for DNMT3B antibody (AA 1-150) (ABIN5542517)

Target

See all DNMT3B Antibodies
DNMT3B (DNA (Cytosine-5-)-Methyltransferase 3 beta (DNMT3B))

Reactivity

  • 94
  • 59
  • 36
  • 7
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 93
  • 6
  • 2
  • 1
Mouse

Clonality

  • 86
  • 16
Monoclonal

Conjugate

  • 47
  • 5
  • 5
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
This DNMT3B antibody is un-conjugated

Application

  • 84
  • 39
  • 29
  • 28
  • 15
  • 13
  • 13
  • 11
  • 8
  • 2
  • 2
  • 1
  • 1
ELISA, Flow Cytometry (FACS), Immunocytochemistry (ICC)

Clone

4D1A2E5
  • Binding Specificity

    • 17
    • 16
    • 8
    • 7
    • 7
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-150

    Purpose

    DNMT3B Antibody

    Purification

    Purified antibody

    Immunogen

    Purified recombinant fragment of human DNMT3B (AA: 1-150) expressed in E. Coli.

    Isotype

    IgG2a
  • Application Notes

    ELISA: 1/10000

    FCM: 1/200 - 1/400

    ICC: 1/200 - 1/1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified antibody in PBS with 0.05 % sodium azide.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Target

    DNMT3B (DNA (Cytosine-5-)-Methyltransferase 3 beta (DNMT3B))

    Alternative Name

    DNMT3B

    Background

    CpG methylation is an epigenetic modification that is important for embryonic development, imprinting, and X-chromosome inactivation. Studies in mice have demonstrated that DNA methylation is required for mammalian development. This gene encodes a DNA methyltransferase which is thought to function in de novo methylation, rather than maintenance methylation. The protein localizes primarily to the nucleus and its expression is developmentally regulated. Mutations in this gene cause the immunodeficiency-centromeric instability-facial anomalies (ICF) syndrome. Eight alternatively spliced transcript variants have been described. The full length sequences of variants 4 and 5 have not been determined.

    Molecular Weight

    95.8 kDa

    Gene ID

    1789

    UniProt

    Q9UBC3
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