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Hexokinase antibody (AA 1-917)

Reactivity: Human WB, ELISA, IF, ICC Host: Mouse Monoclonal 4D7 unconjugated
Catalog No. ABIN7596072
  • 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)
    Purpose
    Human Hexokinase antibody
    Purification
    protein-A affinity chromatography
    Immunogen
    Recombinant human Hexokinase1 (1-917aa) purified from E. coli
    Clone
    4D7
    Isotype
    IgG2a kappa
    Top Product
    Discover our top product Hexokinase Primary Antibody
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    Phosphate-Buffered Saline (pH 7.4) with 0.02% Sodium Azide, 10% glycero
    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 fromATP to glucose to form glucose-6-phosphate and ADP. In mammals, four distinct enzymes-types 1 to 4hexokinases-have been identified. The enzyme is found in most cells, but there is tissue specificity for theparticular type of hexokinase. Hexokinase1 is found in the adipose tissue and liver and encodes a ubiquitous formof hexokinase which localizes to the outer membrane of mitochondria. Mutations in this hexokinase1 have beenassociated with hemolytic anemia due to hexokinase deficiency.
    NCBI Accession
    NP_000179
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