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Actin, alpha 1, Skeletal Muscle (ACTA1) (N-Term) Peptide

ACTA1 Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN8093870
$145.08
Plus shipping costs $50.00
100 μg
Shipping to: United States
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Quick Overview for Actin, alpha 1, Skeletal Muscle (ACTA1) (N-Term) Peptide (ABIN8093870)

Target

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

Origin

Human

Source

  • 6
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB)
  • Protein Region

    N-Term

    Purpose

    ACTA1 Peptide - N-terminal region

    Sequence

    GQKDSYVGDE AQSKRGILTL KYPIEHGIIT NWDDMEKIWH HTFYNELRVA
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Comment

    This is a synthetic peptide designed for use in combination with anti-ACTA1 Antibody (ARP60969_P050),. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications. Please inquire for more details.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 µL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Buffer

    Lyophilized powder

    Storage

    -20 °C

    Storage Comment

    For longer periods of storage, store at -20 °C. Avoid repeat freeze-thaw cycles.
  • Target

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

    Background

    Background Information: 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.

    Alternative Symbols: ACTA, ASMA, CFTD, CFTD1, CFTDM, MPFD, NEM1, NEM2, NEM3

    Molecular Weight

    42kDa

    Gene ID

    58

    NCBI Accession

    NP_001091

    UniProt

    P68133
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