Anti-Smooth muscle actin CE/IVD for IHC - Soft tissue pathology

Anti-Smooth muscle actin CE/IVD for IHC - Soft tissue pathology


Alpha Smooth Muscle Actin (α-SMA), encoded by the ACTA2 gene, is a 42 kDa actin isoform that constitutes a major component of the thin filaments of the contractile apparatus in vascular and visceral smooth muscle cells. In addition to its role in contractility, α-SMA contributes to cytoskeletal organization, mechanotransduction, cellular migration, extracellular matrix remodeling, and tissue repair through its expression in activated myofibroblasts. In normal tissues, α-SMA expression is predominantly observed in smooth muscle cells, pericytes, myofibroblasts, and myoepithelial cells, making it a sensitive marker of smooth muscle and myofibroblastic differentiation in diagnostic pathology.

Biological Significance of α-SMA

  • Major component of the thin filaments of the smooth muscle contractile apparatus.
  • Regulates cellular contractility through interactions with myosin motor proteins.
  • Marker of activated myofibroblasts involved in wound healing, fibrosis, and tissue remodeling.
  • Participates in mechanosensing, cellular migration, and extracellular matrix deposition.

Diagnostic Utility of α-SMA in Soft Tissue Pathology

α-SMA immunohistochemistry is routinely employed for the identification and classification of neoplasms exhibiting smooth muscle or myofibroblastic differentiation. It is particularly useful in the evaluation of:

  • Leiomyoma and leiomyosarcoma.
  • Myofibroblastic neoplasms, including inflammatory myofibroblastic tumor and myofibroma.
  • Perivascular tumors such as glomus tumors and myopericytic neoplasms.
  • Spindle cell lesions when interpreted in conjunction with desmin, h-caldesmon, calponin, and muscle-specific actin.
  • Stromal myofibroblast activation and tumor microenvironment remodeling.

Because α-SMA expression is not restricted to smooth muscle cells, it is considered a sensitive but relatively non-specific marker and is typically interpreted as part of a broader immunohistochemical panel.

Key Features of CE/IVD α-SMA Antibodies

  • Validated for formalin-fixed paraffin-embedded (FFPE) tissues.
  • Optimized for standardized and reproducible IHC workflows.
  • Commonly available as highly specific monoclonal antibodies, including the widely used clone 1A4.
  • Characteristic cytoplasmic staining pattern with minimal background reactivity under optimized conditions.
  • Compatible with automated staining platforms and routine diagnostic laboratories.
  • Designed to support CE/IVD-compliant clinical pathology applications requiring high analytical reproducibility and manufacturing consistency.

 

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