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Actin antibody

This anti-Actin antibody is a Rabbit Polyclonal antibody detecting Actin in WB and ELISA. Suitable for Human, Mouse and Rat.
Catalog No. ABIN7000360

Quick Overview for Actin antibody (ABIN7000360)

Target

See all Actin (ACTA1) Antibodies
Actin (ACTA1) (Actin, alpha 1, Skeletal Muscle (ACTA1))

Reactivity

  • 96
  • 50
  • 42
  • 15
  • 10
  • 10
  • 9
  • 7
  • 6
  • 5
  • 5
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 85
  • 32
Rabbit

Clonality

  • 75
  • 39
  • 1
Polyclonal

Conjugate

  • 71
  • 12
  • 11
  • 10
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Actin antibody is un-conjugated

Application

  • 91
  • 64
  • 49
  • 29
  • 28
  • 21
  • 12
  • 11
  • 6
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant protein of human ACTA1

    Isotype

    IgG
  • Application Notes

    WB 1:200-1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.2 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 (ACTA1) (Actin, alpha 1, Skeletal Muscle (ACTA1))

    Alternative Name

    ACTA1

    Background

    The product encoded by this gene belongs to the actin family of proteins, which are highly conserved proteins that play a role in cell motility, structure and integrity. Alpha, beta and gamma actin isoforms have been identified, with alpha actins being a major constituent of the contractile apparatus, while beta and gamma actins are involved in the regulation of cell motility. This actin is an alpha actin that is found in skeletal muscle. Mutations in this gene cause nemaline myopathy type 3, congenital myopathy with excess of thin myofilaments, congenital myopathy with cores, and congenital myopathy with fiber-type disproportion, diseases that lead to muscle fiber defects.

    Molecular Weight

    42 kDa

    UniProt

    P68133

    Pathways

    Caspase Cascade in Apoptosis, Myometrial Relaxation and Contraction, Skeletal Muscle Fiber Development
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