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TMEM176A antibody

TMEM176A Reactivity: Rat IF, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7075995
  • Target See all TMEM176A products
    TMEM176A (Transmembrane Protein 176A (TMEM176A))
    Reactivity
    • 15
    • 15
    • 7
    • 1
    Rat
    Host
    • 21
    • 1
    Rabbit
    Clonality
    • 21
    • 1
    Polyclonal
    Conjugate
    • 8
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This TMEM176A antibody is un-conjugated
    Application
    • 22
    • 13
    • 13
    • 5
    • 4
    • 3
    • 1
    • 1
    Immunofluorescence (IF), Immunohistochemistry (IHC)
    Cross-Reactivity
    Rat
    Purification
    Affinity purification
    Immunogen
    KLH conjugated Synthetic peptide corresponding to Mouse TMEM176A
  • Application Notes
    IHC/IF (R) 1:500-1:1000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS, pH 7.4, 0.02 % 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
    -20 °C
  • Target
    TMEM176A (Transmembrane Protein 176A (TMEM176A))
    Alternative Name
    TMEM176A (TMEM176A Products)
    Synonyms
    GS188 antibody, HCA112 antibody, 0610011I04Rik antibody, AU040201 antibody, AU041743 antibody, Keg2 antibody, 0610011i04rik antibody, RGD1310725 antibody, CL1 antibody, transmembrane protein 176A antibody, TMEM176A antibody, Tmem176a antibody
    Background
    TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5 % of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance.
    Gene ID
    66058
    UniProt
    Q9DCS1
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