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IHC-P analysis of human small bowel tissue using GTX44499 alpha Smooth Muscle Actin antibody [alphasm-1]. Note cytoplasmic staining of the muscularis mucosa, vascular walls and smooth muscle fibers in the lamina propria.
IHC-P analysis of human small bowel tissue using GTX44499 alpha Smooth Muscle Actin antibody [alphasm-1]. Note cytoplasmic staining of the muscularis mucosa, vascular walls and smooth muscle fibers in the lamina propria.
IHC-P analysis of human small bowel tissue using GTX44499 alpha Smooth Muscle Actin antibody [alphasm-1]. Note cytoplasmic staining of the muscularis mucosa, vascular walls and smooth muscle fibers in the lamina propria.

alpha Smooth Muscle Actin antibody [alphasm-1]

GTX44499
GeneTex
ApplicationsImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetACTA2
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Overview

  • Supplier
    GeneTex
  • Product Name
    alpha Smooth Muscle Actin antibody [alphasm-1]
  • Delivery Days Customer
    9
  • Application Supplier Note
    IHC-P: 1:50. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    alphasm-1
  • Concentration
    > 4.5 ug/ml
  • Conjugate
    Unconjugated
  • Gene ID59
  • Target name
    ACTA2
  • Target description
    actin alpha 2, smooth muscle
  • Target synonyms
    actin, alpha 2, smooth muscle, aorta; actin, aortic smooth muscle; ACTSA; alpha-cardiac actin; cell growth-inhibiting gene 46 protein
  • Host
    Mouse
  • Isotype
    IgG2a
  • Protein IDP62736
  • Protein Name
    Actin, aortic smooth muscle
  • Scientific Description
    This gene encodes one of six different actin proteins. Actins are highly conserved proteins that are involved in cell motility, structure, integrity, and intercellular signaling. The encoded protein is a smooth muscle actin that is involved in vascular contractility and blood pressure homeostasis. Mutations in this gene cause a variety of vascular diseases, such as thoracic aortic disease, coronary artery disease, stroke, and Moyamoya disease, as well as multisystemic smooth muscle dysfunction syndrome. [provided by RefSeq, Sep 2017]
  • Storage Instruction
    2°C to 8°C
  • UNSPSC
    12352203

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