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Liver Arginase antibody (Arg1, N-Term)

The Rabbit Polyclonal anti-Liver Arginase antibody has been validated for WB and IHC. It is suitable to detect Liver Arginase in samples from Human, Rat and Dog.
Catalog No. ABIN629657

Quick Overview for Liver Arginase antibody (Arg1, N-Term) (ABIN629657)

Target

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

Reactivity

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Human, Rat, Dog

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)
  • Binding Specificity

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    Arg1, N-Term

    Specificity

    Arginase 1 antibody was raised against the N terminal of ARG1

    Purification

    Purified

    Immunogen

    Arginase 1 antibody was raised using the N terminal of ARG1 corresponding to a region with amino acids HSLAIGSISGHARVHPDLGVIWVDAHTDINTPLTTTSGNLHGQPVSFLLK
  • Application Notes

    WB: 5 µg/mL, IHC: 4-8 µg/mL
    Optimal conditions should be determined by the investigator.

    Comment

    Arginase 1 Blocking Peptide, (ABIN939241), is also available for use as a blocking control in assays to test for specificity of this Arginase 1 antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of ARG1 antibody in PBS

    Concentration

    Lot specific

    Buffer

    PBS

    Handling Advice

    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Target

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

    Alternative Name

    Arginase 1

    Background

    Arginase catalyzes the hydrolysis of arginine to ornithine and urea. The type I isoform of ARG1, 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.

    Molecular Weight

    35 kDa (MW of target protein)

    Pathways

    Cellular Response to Molecule of Bacterial Origin
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