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Liver Arginase antibody (C-Term)

This anti-Liver Arginase antibody is a Mouse Monoclonal antibody detecting Liver Arginase in WB, IHC and IF. Suitable for Human.
Catalog No. ABIN6295107

Quick Overview for Liver Arginase antibody (C-Term) (ABIN6295107)

Target

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

Reactivity

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  • 1
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Human

Host

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Mouse

Clonality

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  • 75
  • 1
Monoclonal

Conjugate

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  • 1
  • 1
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  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Liver Arginase antibody is un-conjugated

Application

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

    • 32
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    • 16
    • 13
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    C-Term

    Purpose

    Mouse anti-Human Arginase 1 Antibody [Sodium Azide Free]

    Specificity

    Cytoplasmic

    Purification

    A C-terminal recombinant protein fragment from ARG1 was used as the immunogen for the Arginase 1 antibody.

    Immunogen

    A C-terminal recombinant protein fragment from ARG1 was used as the immunogen for the Arginase 1 antibody.
  • Application Notes

    Immunofluorescence: 1-2 μg/mL
    Western blot: 0.5-1 μg/mL
    Immunohistochemistry (FFPE): 2-4 μg/mL for 30 min at RT (1)
    Prediluted format: incubate for 30 min at RT (2)

    Restrictions

    For Research Use only
  • Buffer

    In 1X PBS, BSA free, sodium azide free

    Preservative

    Azide free

    Storage

    4 °C,-20 °C

    Storage Comment

    2-8°C. The azide-free format should be aliquoted and stored at -20°C or colder.
  • Target

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

    Alternative Name

    Arginase-1

    Background

    Target Description: 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 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. [RefSeq]

    Gene Symbol: ARG1

    Gene ID

    383

    UniProt

    P05089

    Pathways

    Cellular Response to Molecule of Bacterial Origin
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