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Hexokinase Antikörper (AA 1-917)

Dieses Maus Monoklonal-Antikörper erkennt spezifisch Hexokinase in WB, ELISA, IF und ICC. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN7596072

Kurzübersicht für Hexokinase Antikörper (AA 1-917) (ABIN7596072)

Target

Alle Hexokinase Antikörper anzeigen
Hexokinase

Reaktivität

  • 2
  • 2
  • 1
Human

Wirt

  • 3
  • 2
Maus

Klonalität

  • 3
  • 2
Monoklonal

Konjugat

  • 4
  • 1
Dieser Hexokinase Antikörper ist unkonjugiert

Applikation

Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunocytochemistry (ICC)

Klon

4D7
  • Bindungsspezifität

    AA 1-917

    Verwendungszweck

    Human Hexokinase antibody

    Aufreinigung

    protein-A affinity chromatography

    Immunogen

    Recombinant human Hexokinase1 (1-917aa) purified from E. coli

    Isotyp

    IgG2a kappa
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1 mg/mL

    Buffer

    Phosphate-Buffered Saline (pH 7.4) with 0.02% Sodium Azide, 10% glycero

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    4 °C,-20 °C,-80 °C

    Informationen zur Lagerung

    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

    Hintergrund

    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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