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ZMYM3 antibody (AA 140-300)

This Rabbit Polyclonal antibody specifically detects ZMYM3 in WB and IHC. It exhibits reactivity toward Human.
Catalog No. ABIN6150453

Quick Overview for ZMYM3 antibody (AA 140-300) (ABIN6150453)

Target

See all ZMYM3 Antibodies
ZMYM3 (Zinc Finger Protein 261 (ZMYM3))

Reactivity

  • 20
  • 10
  • 6
  • 5
  • 5
  • 5
  • 5
  • 3
  • 3
  • 2
Human

Host

  • 18
  • 2
Rabbit

Clonality

  • 18
  • 2
Polyclonal

Conjugate

  • 16
  • 2
  • 1
  • 1
This ZMYM3 antibody is un-conjugated

Application

  • 13
  • 8
  • 6
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Binding Specificity

    • 5
    • 4
    • 3
    • 3
    • 1
    • 1
    AA 140-300

    Sequence

    LLEPLAPDSP ITLQSPHIEE EETTSIATAR RGSPGQEEEL PQGQPQSPNA PPSPSVGETL GDGINSSQTK PGGSSPPAHP SLPGDGLTAK ASEKPPERKR SERVRRAEPP KPEVVDSTES IPVSDEDSDA MVDDPNDEDF VPFRPRRSPR MSLRSSVSQR A

    Cross-Reactivity

    Human

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 140-300 of human ZMYM3 (NP_001164634.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IHC,1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    ZMYM3 (Zinc Finger Protein 261 (ZMYM3))

    Alternative Name

    ZMYM3

    Background

    This gene is located on the X chromosome and is subject to X inactivation. It is highly conserved in vertebrates and most abundantly expressed in the brain. The encoded protein is a component of histone deacetylase-containing multiprotein complexes that function through modifying chromatin structure to keep genes silent. A chromosomal translocation (X,13) involving this gene is associated with X-linked mental retardation. Several alternatively spliced transcript variants have been found for this gene.,ZMYM3,DXS6673E,MYM,XFIM,ZNF198L2,ZNF261,Epigenetics & Nuclear Signaling,ZMYM3

    Molecular Weight

    52 kDa/151 kDa/152 kDa

    Gene ID

    9203

    UniProt

    Q14202
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