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Liver Arginase antibody (AA 1-292)

The Rabbit Polyclonal anti-Liver Arginase antibody has been validated for WB, IHC and IF. It is suitable to detect Liver Arginase in samples from Human.
Catalog No. ABIN1885889

Quick Overview for Liver Arginase antibody (AA 1-292) (ABIN1885889)

Target

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

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This Liver Arginase antibody is un-conjugated

Application

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Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Binding Specificity

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    AA 1-292

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 1 and 292 of arginase I
  • Application Notes

    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunohistochemistry: 1.100-1.500
    Immunofluorescence: 1.100-1.200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Target

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

    Alternative Name

    arginase I

    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.[provided by RefSeq]

    Molecular Weight

    35 kDa

    Gene ID

    383

    NCBI Accession

    NM_000045, NP_000036

    Pathways

    Cellular Response to Molecule of Bacterial Origin
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