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Liver Arginase antibody

This Mouse Monoclonal antibody specifically detects Liver Arginase in ELISA, IHC and FACS. It exhibits reactivity toward Human.
Catalog No. ABIN7193719

Quick Overview for Liver Arginase antibody (ABIN7193719)

Target

See all Liver Arginase (ARG1) Antibodies
Liver Arginase (ARG1) (Arginase, Liver (ARG1))

Reactivity

  • 148
  • 60
  • 45
  • 12
  • 10
  • 5
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 115
  • 60
  • 5
  • 3
  • 2
Mouse

Clonality

  • 109
  • 75
  • 1
Monoclonal

Conjugate

  • 103
  • 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
This Liver Arginase antibody is un-conjugated

Application

  • 111
  • 73
  • 60
  • 31
  • 31
  • 21
  • 20
  • 16
  • 14
  • 13
  • 10
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
ELISA, Immunohistochemistry (IHC), Flow Cytometry (FACS)

Clone

7D1D10
  • Purpose

    ARG1 Antibody

    Purification

    Purified antibody

    Immunogen

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

    Isotype

    IgG1
  • Application Notes

    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.

    Preservative

    Sodium azide

    Precaution of Use

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

    Storage

    4 °C,-20 °C

    Storage Comment

    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))

    Alternative Name

    ARG1

    Background

    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]

    Molecular Weight

    34.7 kDa

    Gene ID

    383

    UniProt

    P05089

    Pathways

    Cellular Response to Molecule of Bacterial Origin
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