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WRB antibody

WRB Reactivity: Mouse, Rat IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7262941
  • Target See all WRB Antibodies
    WRB (Tryptophan Rich Basic Protein (WRB))
    Reactivity
    • 13
    • 2
    • 1
    Mouse, Rat
    Host
    • 8
    • 5
    • 1
    Rabbit
    Clonality
    • 12
    • 2
    Polyclonal
    Conjugate
    • 10
    • 2
    • 1
    • 1
    This WRB antibody is un-conjugated
    Application
    • 10
    • 8
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human WRB (NP_004618.2).
    Isotype
    IgG
  • 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
    WRB (Tryptophan Rich Basic Protein (WRB))
    Alternative Name
    WRB (WRB Products)
    Synonyms
    pwi antibody, wu:ft06h05 antibody, zgc:101856 antibody, chd5 antibody, MGC89989 antibody, WRB antibody, UCP-1 antibody, DKFZp469L094 antibody, wrb antibody, mCHD5 antibody, MGC115192 antibody, CHD5 antibody, 5530402J05Rik antibody, C030018G21Rik antibody, Chd5 antibody, tryptophan rich basic protein antibody, tryptophan rich basic protein L homeolog antibody, WRB antibody, wrb antibody, wrb.L antibody, Wrb antibody
    Background
    This gene encodes a basic nuclear protein of unknown function. The gene is widely expressed in adult and fetal tissues. Since the region proposed to contain the gene(s) for congenital heart disease (CHD) in Down syndrome (DS) patients has been restricted to 21q22.2-22.3, this gene, which maps to 21q22.3, has a potential role in the pathogenesis of Down syndrome congenital heart disease. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
    Gene ID
    7485
    UniProt
    O00258
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