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Actin, gamma 1 antibody

This Rabbit Polyclonal antibody specifically detects Actin, gamma 1 in WB and ELISA. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN7001540

Quick Overview for Actin, gamma 1 antibody (ABIN7001540)

Target

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

Reactivity

  • 37
  • 19
  • 13
  • 5
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 32
  • 7
  • 3
Rabbit

Clonality

  • 35
  • 7
Polyclonal

Conjugate

  • 26
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Actin, gamma 1 antibody is un-conjugated

Application

  • 30
  • 17
  • 13
  • 9
  • 8
  • 8
  • 7
  • 6
  • 4
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant protein of human ACTG1

    Isotype

    IgG
  • Application Notes

    WB 1:500-1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.4 mg/mL

    Buffer

    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    Actin, gamma 1 (ACTG1)

    Alternative Name

    ACTG1

    Background

    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.

    Molecular Weight

    42 kDa

    UniProt

    P63261

    Pathways

    Myometrial Relaxation and Contraction, Cell-Cell Junction Organization
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