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Liver Arginase anticorps

L’anticorps Souris Monoclonal anti-Liver Arginase a été validé pour WB, IHC et FACS. Il convient pour détecter Liver Arginase dans des échantillons de Humain.
N° du produit ABIN2716328

Aperçu rapide pour Liver Arginase anticorps (ABIN2716328)

Antigène

Voir toutes Liver Arginase (ARG1) Anticorps
Liver Arginase (ARG1) (Arginase, Liver (ARG1))

Reactivité

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Humain

Hôte

  • 113
  • 41
  • 5
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  • 2
Souris

Clonalité

  • 107
  • 56
  • 1
Monoclonal

Conjugué

  • 98
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  • 1
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Cet anticorp Liver Arginase est non-conjugé

Application

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Western Blotting (WB), Immunohistochemistry (IHC), Flow Cytometry (FACS)

Clone

4E6
  • Attributs du produit

    Homo sapiens arginase, liver (ARG1)

    Purification

    Purified from mouse ascites fluids by affinity chromatography

    Immunogène

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

    Isotype

    IgG1
  • Indications d'application

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

    Commentaires

    The concentration of the product may vary between diferrent lots.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5-1.0 mg/mL

    Buffer

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

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    -20 °C
  • Antigène

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

    Autre désignation

    ARG1

    Sujet

    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.

    Poids moléculaire

    34.6 kDa

    ID gène

    383

    NCBI Accession

    NM_000045

    HGNC

    383

    Pathways

    Cellular Response to Molecule of Bacterial Origin
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