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HAL Antikörper

Dieses 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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