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Liver Arginase anticorps

Cet anticorps Souris Monoclonal détecte spécifiquement Liver Arginase dans ELISA, IHC et FACS. Il présente une réactivité envers Humain.
N° du produit ABIN7193719

Aperçu rapide pour Liver Arginase anticorps (ABIN7193719)

Antigène

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

Reactivité

  • 126
  • 63
  • 47
  • 12
  • 10
  • 5
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 113
  • 41
  • 5
  • 3
  • 2
Souris

Clonalité

  • 107
  • 56
  • 1
Monoclonal

Conjugué

  • 98
  • 11
  • 11
  • 6
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Liver Arginase est non-conjugé

Application

  • 111
  • 57
  • 51
  • 30
  • 23
  • 21
  • 15
  • 14
  • 13
  • 11
  • 10
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
ELISA, Immunohistochemistry (IHC), Flow Cytometry (FACS)

Clone

7D1D10
  • Fonction

    ARG1 Antibody

    Purification

    Purified antibody

    Immunogène

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

    Isotype

    IgG1
  • Indications d'application

    ELISA: 1/10000

    FCM: 1/200-1/400

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified antibody in PBS with 0.05 % 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

    4 °C,-20 °C

    Stockage commentaire

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • 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. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]

    Poids moléculaire

    34.7 kDa

    ID gène

    383

    UniProt

    P05089

    Pathways

    Cellular Response to Molecule of Bacterial Origin
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