Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

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

ACTA1 Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN972856
  • Target See all Actin (ACTA1) products
    Actin (ACTA1) (Actin, alpha 1, Skeletal Muscle (ACTA1))
    Protein Region
    N-Term
    Origin
    Human
    Source
    • 4
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Sequence
    GQKDSYVGDE AQSKRGILTL KYPIEHGIIT NWDDMEKIWH HTFYNELRVA
    Characteristics
    This is a synthetic peptide designed for use in combination with anti-ACTA1 Antibody. 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.
    Purification
    Purified
  • Application Notes
    Each Investigator should determine their own optimal working dilution for specific applications.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Concentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Handling Advice
    Avoid repeated freeze-thaw cycles.
    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
    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.

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

    Protein Interaction Partner: ABL1,ACTA1,ACTR10,ACTR1B,ADSS,AFAP1,AIF1,CCIN,CCT4,CCT5,CFL1,CLIC5,CNN1,CORO2B,COTL1,CTNND1,CTTN,CYFIP1,CYTH1,DLG1,DMD,DNASE1,DNMBP,DTNA,EGFR,EPB41,EPB41L2,EPS8,FGD4,FHOD1,FSCN1,GAS2,GAS7,GC,GSN,HCLS1,HIP1R,IQGAP1,ITGA2,ITPKA,JUB,KIF23,KLHL20,LASP1,MACF1,

    Protein Size: 377
    Molecular Weight
    42 kDa
    Gene ID
    58
    NCBI Accession
    NM_001100, NP_001091
    UniProt
    P68133
You are here:
Support