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Liver Arginase antibody (AA 1-292)

The Rabbit Polyclonal anti-Liver Arginase antibody is suitable to detect Liver Arginase in samples from Human. It has been validated for WB, IHC and IF.
Catalog No. ABIN1885889
$526.90
Plus shipping costs $50.00
100 μL
Shipping to: United States
Delivery in 6 to 9 Business Days

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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