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HAL Antikörper

Dieser Anti-HAL Antikörper ist ein Kaninchen Polyklonal Antikörper zur Detektion von HAL in WB. Geeignet für Human.
Produktnummer ABIN7466882

Kurzübersicht für HAL Antikörper (ABIN7466882)

Target

Alle HAL Antikörper anzeigen
HAL (Histidine Ammonia-Lyase (HAL))

Reaktivität

  • 19
  • 9
  • 8
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Wirt

  • 16
  • 3
Kaninchen

Klonalität

  • 18
  • 1
Polyklonal

Konjugat

  • 15
  • 2
  • 1
  • 1
Dieser HAL Antikörper ist unkonjugiert

Applikation

  • 14
  • 9
  • 6
  • 3
  • 1
  • 1
Western Blotting (WB)
  • Kreuzreaktivität

    Maus

    Aufreinigung

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein encompassing a sequence within the center region of human HAL. The exact sequence is proprietary.

    Isotyp

    IgG
  • Applikationshinweise

    WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Kommentare

    Positive Control: Mouse liver

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1 mg/mL

    Buffer

    1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.01 % Thimerosal

    Konservierungsmittel

    Thimerosal (Merthiolate)

    Vorsichtsmaßnahmen

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Target

    HAL (Histidine Ammonia-Lyase (HAL))

    Andere Bezeichnung

    histidine ammonia-lyase

    Hintergrund

    Histidine ammonia-lyase , HIS , HSTD,Histidine ammonia-lyase is a cytosolic enzyme catalyzing the first reaction in histidine catabolism, the nonoxidative deamination of L-histidine to trans-urocanic acid. Histidine ammonia-lyase defects cause histidinemia which is characterized by increased histidine and histamine and decreased urocanic acid in body fluids [provided by RefSeq]

    Molekulargewicht

    73 kDa

    Gen-ID

    3034

    UniProt

    P42357
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