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Liver Arginase Antikörper

Der Maus Monoklonal Anti-Liver Arginase-Antikörper wurde für WB, IHC und FACS validiert. Er ist geeignet, Liver Arginase in Proben von Human zu detektieren.
Produktnummer ABIN2716328

Kurzübersicht für Liver Arginase Antikörper (ABIN2716328)

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

  • 111
  • 74
  • 61
  • 31
  • 31
  • 21
  • 21
  • 17
  • 14
  • 13
  • 10
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Flow Cytometry (FACS)

Klon

4E6
  • Produktmerkmale

    Homo sapiens arginase, liver (ARG1)

    Aufreinigung

    Purified from mouse ascites fluids by affinity chromatography

    Immunogen

    Full length human recombinant protein of human ARG1 (NP_000036) produced in HEK293T cell.

    Isotyp

    IgG1
  • Applikationshinweise

    WB 1:1000~2000, IHC 1:50, FLOW 1:100

    Kommentare

    The concentration of the product may vary between diferrent lots.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    0.5-1.0 mg/mL

    Buffer

    PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % 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

    -20 °C
  • 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.

    Molekulargewicht

    34.6 kDa

    Gen-ID

    383

    NCBI Accession

    NM_000045

    HGNC

    383

    Pathways

    Cellular Response to Molecule of Bacterial Origin
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