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ASL Antikörper (AA 86-335)

Der Kaninchen Polyklonal Anti-ASL-Antikörper wurde für WB und IHC validiert. Er ist geeignet, ASL in Proben von Human zu detektieren.
Produktnummer ABIN1886687

Kurzübersicht für ASL Antikörper (AA 86-335) (ABIN1886687)

Target

Alle ASL Antikörper anzeigen
ASL (Argininosuccinate Lyase (ASL))

Reaktivität

  • 60
  • 15
  • 11
  • 6
  • 6
  • 6
  • 6
  • 6
  • 5
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
Human

Wirt

  • 55
  • 5
Kaninchen

Klonalität

  • 57
  • 3
Polyklonal

Konjugat

  • 31
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser ASL Antikörper ist unkonjugiert

Applikation

  • 40
  • 13
  • 13
  • 13
  • 12
  • 12
  • 7
  • 6
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Bindungsspezifität

    • 15
    • 12
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 86-335

    Aufreinigung

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 86 and 335 of Human ASL
  • Applikationshinweise

    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunohistochemistry: 1.50-1.500

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Konservierungsmittel

    Thimerosal (Merthiolate)

    Vorsichtsmaßnahmen

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Lagerung

    4 °C/-20 °C

    Informationen zur Lagerung

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Target

    ASL (Argininosuccinate Lyase (ASL))

    Andere Bezeichnung

    Argininosuccinate Lyase

    Hintergrund

    This gene encodes a member of the lyase 1 family.The encoded protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle.Mutations in this gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency.A nontranscribed pseudogene is also located on the long arm of chromosome 22.Alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq]

    Molekulargewicht

    49 kDa

    Gen-ID

    435

    NCBI Accession

    NP_001020117, NM_001024946

    Pathways

    Response to Growth Hormone Stimulus
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