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Last updated: 2014/7/7
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ACTA1 monoclonal antibody, clone 5C5.F8.C7

  • Catalog # : MAB2075
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  • Specification
  • Product Description:
  • Mouse monoclonal antibody raised against synthetic peptide of ACTA1.
  • Immunogen:
  • A synthetic peptide corresponding to N-terminus of human ACTA1.
  • Host:
  • Mouse
  • Theoretical MW (kDa):
  • 42
  • Reactivity:
  • Human
  • Form:
  • Liquid
  • Purification:
  • Protein A purification
  • Concentration:
  • Lot specific
  • Isotype:
  • IgM
  • Quality Control Testing:
  • Antibody Reactive Against Synthetic Peptide.
  • Recommend Usage:
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (Formalin/PFA-fixed paraffin-embedded sections) (1:50)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In 10 mM PBS, pH 7.4 (1% BSA, 0.1% sodium azide)
  • Storage Instruction:
  • Store at 4°C.
  • Note:
  • This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
  • Applications
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemical staining of ACTA1 on formalin fixed, paraffin embedded human skeletal muscle with ACTA1 monoclonal antibody, clone 5C5F8C7 (Cat # MAB2075).
  • Application Image
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • enlarge
  • Gene Information
  • Entrez GeneID:
  • 58
  • Gene Name:
  • ACTA1
  • Gene Alias:
  • ACTA,ASMA,CFTD,CFTD1,CFTDM,MPFD,NEM1,NEM2,NEM3
  • Gene Description:
  • actin, alpha 1, skeletal muscle
  • Gene Summary:
  • 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
  • Other Designations:
  • OTTHUMP00000036123,alpha skeletal muscle actin
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