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Hexokinase antibody (AA 1-917)

Reactivity: Human WB, ELISA, IF, ICC Host: Mouse Monoclonal 4D7 unconjugated
Catalog No. ABIN306422
  • Target See all Hexokinase Antibodies
    Hexokinase
    Binding Specificity
    AA 1-917
    Reactivity
    • 2
    • 2
    • 1
    Human
    Host
    • 3
    • 2
    Mouse
    Clonality
    • 3
    • 2
    Monoclonal
    Conjugate
    • 4
    • 1
    This Hexokinase antibody is un-conjugated
    Application
    Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunocytochemistry (ICC)
    Purification
    The antibody was purified from mouse ascitic fluids by protein-G affinity chromatography
    Immunogen
    Recombinant human Hexokinase1 (1-917aa) purified from E. coli
    Clone
    4D7
    Isotype
    IgG2a kappa
  • Application Notes
    Recommended dilution 1:1000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    In Phosphate-Buffered Saline (pH7.4) with 0.1% 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
    4 °C,-20 °C,-80 °C
    Storage Comment
    Can be stored at +2°C to +8°C for 1 week. For long term storage, aliquot and store at -20°C to -80°C. Avoid repeated freezing and thawing cycles.
  • Target
    Hexokinase
    Abstract
    Hexokinase Products
    Background
    Hexokinase is the first enzyme in the glycolytic pathway, catalyzing the transfer of a phosphoryl group from ATP to glucose to form glucose-6-phosphate and ADP. In mammals, four distinct enzymes-types 1 to 4 hexokinases-have been identified. The enzyme is found in most cells, but there is tissue specificity for the particular type of hexokinase. Hexokinase1 is found in the adipose tissue and liver and encodes a ubiquitous form of hexokinase which localizes to the outer membrane of mitochondria. Mutations in this hexokinase1 have been associated with hemolytic anemia due to hexokinase deficiency.
    NCBI Accession
    NP_000179
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