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Liver Arginase Antikörper

Dieses Anti-Liver Arginase-Antikörper ist ein Maus Monoklonal-Antikörper zur Detektion von Liver Arginase in ELISA und IHC. Geeignet für Human.
Produktnummer ABIN7193718

Kurzübersicht für Liver Arginase Antikörper (ABIN7193718)

Target

Alle Liver Arginase (ARG1) Antikörper anzeigen
Liver Arginase (ARG1) (Arginase, Liver (ARG1))

Reaktivität

  • 148
  • 61
  • 46
  • 12
  • 10
  • 5
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 115
  • 61
  • 5
  • 3
  • 2
Maus

Klonalität

  • 109
  • 76
  • 1
Monoklonal

Konjugat

  • 104
  • 13
  • 11
  • 6
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser Liver Arginase Antikörper ist unkonjugiert

Applikation

  • 112
  • 74
  • 60
  • 32
  • 31
  • 21
  • 21
  • 17
  • 14
  • 13
  • 10
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
ELISA, Immunohistochemistry (IHC)

Klon

6B4B11
  • Verwendungszweck

    ARG1 Antibody

    Aufreinigung

    Purified antibody

    Immunogen

    Purified recombinant fragment of human ARG1 (AA: (1-322)) expressed in E. Coli.

    Isotyp

    IgG1
  • Applikationshinweise

    ELISA: 1/10000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    Purified antibody in PBS with 0.05 % sodium azide.

    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

    Informationen zur Lagerung

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Target

    Liver Arginase (ARG1) (Arginase, Liver (ARG1))

    Andere Bezeichnung

    ARG1

    Hintergrund

    Arginase catalyzes the hydrolysis of arginine to ornithine and urea. At least two isoforms of mammalian arginase exist (types I and II) which differ in their tissue distribution, subcellular localization, immunologic crossreactivity and physiologic function. The type I isoform encoded by this gene, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]

    Molekulargewicht

    34.7 kDa

    Gen-ID

    383

    UniProt

    P05089

    Pathways

    Cellular Response to Molecule of Bacterial Origin
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