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STK32A antibody

STK32A Reactivity: Human, Mouse WB, ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7247471
  • Target See all STK32A Antibodies
    STK32A (serine/threonine Kinase 32A (STK32A))
    Reactivity
    • 35
    • 28
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Human, Mouse
    Host
    • 45
    • 3
    Rabbit
    Clonality
    • 45
    • 3
    Polyclonal
    Conjugate
    • 21
    • 5
    • 4
    • 4
    • 4
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This STK32A antibody is un-conjugated
    Application
    • 39
    • 30
    • 15
    • 3
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogen
    Fusion protein of human STK32A
    Isotype
    IgG
    Top Product
    Discover our top product STK32A Primary Antibody
  • Application Notes
    WB 1:500-1:2000, IHC 1:100-1:200, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.68 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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
    STK32A (serine/threonine Kinase 32A (STK32A))
    Alternative Name
    STK32A (STK32A Products)
    Synonyms
    YANK1 antibody, A930015B13Rik antibody, serine/threonine kinase 32A antibody, STK32A antibody, Stk32a antibody
    Background
    STK32A (serine/threonine kinase 32A), also known as YANK1, is a 396 amino acid protein that belongs to the superfamily of serine/threonine protein kinases and exists as three isoforms. The gene encoding STK32A maps to human chromosome 5, which is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene.
    Molecular Weight

    Observed_MW: Refer to figures

    Calculated_MW: 46 kDa

    UniProt
    Q8WU08
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