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Actin antibody

The Rabbit Monoclonal anti-Actin antibody has been validated for WB and IF. It is suitable to detect Actin in samples from Human.
Catalog No. ABIN1680683

Quick Overview for Actin antibody (ABIN1680683)

Target

See all Actin Antibodies
Actin

Reactivity

  • 102
  • 78
  • 74
  • 27
  • 21
  • 20
  • 12
  • 11
  • 6
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 88
  • 42
  • 3
  • 1
  • 1
  • 1
Rabbit

Clonality

  • 80
  • 56
Monoclonal

Conjugate

  • 79
  • 6
  • 4
  • 4
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
This Actin antibody is un-conjugated

Application

  • 108
  • 42
  • 32
  • 29
  • 28
  • 27
  • 26
  • 22
  • 18
  • 16
  • 15
  • 3
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthesized peptide derived from human alpha-Actin-1 (ACTA1)

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IF,1:50 - 1:200

    Restrictions

    For Research Use only
  • Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    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

    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. [provided by RefSeq, Jul 2008],ACTA, ASMA, CFTD, CFTD1, CFTDM, MPFD, NEM1, NEM2, NEM3, SHPM,Cardiovascular,Cell Biology & Developmental Biology,Cytoskeleton,Cytoskeleton_Actins,Cytoskeleton_Microfilaments,Heart,Heart_Contractility,Signal Transduction,Actin

    Molecular Weight

    42 kDa

    Gene ID

    58

    UniProt

    P68133
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