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Actin, alpha 1, Skeletal Muscle (ACTA1) Peptid

ACTA1 Reaktivität: Säugetier Wirt: Synthetic BP, WB, IHC
Produktnummer ABIN936401

Kurzübersicht für Actin, alpha 1, Skeletal Muscle (ACTA1) Peptid (ABIN936401)

Target

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

Spezies

Säugetier

Quelle

  • 4
Synthetic

Applikation

Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
  • Protein-Typ

    Synthetic

    Sequenz

    STMKIKIIAP PERKYSVWIG GSILASLSTF QQMWITKQEY DEAGPSIVHR

    Produktmerkmale

    A synthetic peptide for use as a blocking control in assays to test for specificity of ACTA1 antibody,
    Alternative Names: ACTA1 control peptide, ACTA1 antibody Blocking Peptide, Anti-ACTA1 Blocking Peptide, actin, alpha 1, skeletal muscle Blocking Peptide, ACTA Blocking Peptide, ASMA Blocking Peptide, CFTD Blocking Peptide, CFTD1 Blocking Peptide, CFTDM Blocking Peptide, MPFD Blocking Peptide, NEM1 Blocking Peptide, NEM2 Blocking Peptide, NEM3 Blocking Peptide, ACTA1, ACTA-1, ACTA 1, ACTA-1 Blocking Peptide, ACTA 1 Blocking Peptide
  • Applikationshinweise

    Optimal conditions should be determined by the investigator

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.

    Buffer

    PBS

    Handhabung

    Avoid repeated freeze/thaw cycles.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at -20 °C long term.
  • Target

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

    Hintergrund

    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.

    Molekulargewicht

    42 kDa
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