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Actin, gamma 1 antibody (Biotin)

This anti-Actin, gamma 1 antibody is a Rabbit Polyclonal antibody detecting Actin, gamma 1 in WB and ELISA. Suitable for Human.
Catalog No. ABIN6297828

Quick Overview for Actin, gamma 1 antibody (Biotin) (ABIN6297828)

Target

See all Actin, gamma 1 (ACTG1) Antibodies
Actin, gamma 1 (ACTG1)

Reactivity

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  • 20
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  • 5
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  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

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  • 3
Rabbit

Clonality

  • 35
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Polyclonal

Conjugate

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  • 1
  • 1
  • 1
  • 1
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  • 1
  • 1
This Actin, gamma 1 antibody is conjugated to Biotin

Application

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Western Blotting (WB), ELISA
  • Purpose

    Rabbit anti-Human ACTG Biotinylated Antibody

    Immunogen

    This antibody was produced from antiserum of rabbits immunized with a recombinant protein immunogen. The IgG fraction was purified by Protein G/A affinity chromatography.
  • Application Notes

    ELISA (recommended dilution= 1:320,000), Western Blotting (recommended dilution= 1:1,000-5,000)

    Restrictions

    For Research Use only
  • Reconstitution

    A separate vial of dilution buffer is provided for reconstitution. The antibody is supplied lyophilized, originally containing PBS, without preservative stabilizers (e. g. sodium azide). The final amount is indicated on the shipping vial.

    Storage

    4 °C,-20 °C,-80 °C

    Storage Comment

    -20°C
  • Target

    Actin, gamma 1 (ACTG1)

    Alternative Name

    ACTG

    Background

    Target Description: Actins are highly conserved proteins that are involved in various types of cell motility, and maintenance of the cytoskeleton. In vertebrates, three main groups of actin isoforms, alpha, beta and gamma have been identified. The alpha actins are found in muscle tissues and are a major constituent of the contractile apparatus. The beta and gamma actins co-exist in most cell types as components of the cytoskeleton, and as mediators of internal cell motility. Actin, gamma 1, encoded by this gene, is a cytoplasmic actin found in non-muscle cells. Mutations in this gene are associated with DFNA20/26, a subtype of autosomal dominant non-syndromic sensorineural progressive hearing loss. Alternative splicing results in multiple transcript variants.

    UniProt

    P63261

    Pathways

    Myometrial Relaxation and Contraction, Cell-Cell Junction Organization
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