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ZMYM3 antibody

ZMYM3 Reactivity: Human IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7256508
  • Target See all ZMYM3 Antibodies
    ZMYM3 (Zinc Finger Protein 261 (ZMYM3))
    Reactivity
    • 21
    • 10
    • 6
    • 5
    • 5
    • 5
    • 5
    • 3
    • 3
    • 2
    Human
    Host
    • 19
    • 2
    Rabbit
    Clonality
    • 19
    • 2
    Polyclonal
    Conjugate
    • 17
    • 2
    • 1
    • 1
    This ZMYM3 antibody is un-conjugated
    Application
    • 14
    • 8
    • 6
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human ZMYM3 (NP_001164634.1).
    Isotype
    IgG
    Top Product
    Discover our top product ZMYM3 Primary Antibody
  • Application Notes
    IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    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 (ZMYM3 Products)
    Synonyms
    ZNF261 antibody, si:ch211-173p18.2 antibody, DXS6673E antibody, MYM antibody, XFIM antibody, ZNF198L2 antibody, 9030216B10Rik antibody, AW122925 antibody, DXS6673El antibody, Zfp261 antibody, zinc finger MYM-type containing 3 antibody, si:ch211-173p18.3 antibody, zinc finger, MYM-type 3 antibody, ZMYM3 antibody, si:ch211-173p18.3 antibody, Zmym3 antibody
    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.
    Gene ID
    9203
    UniProt
    Q14202
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