Anti-Human/Mouse/Rat Alpha Smooth Muscle (αSM) Actin (1A4) – Purified No Carrier Protein
Anti-Human/Mouse/Rat Alpha Smooth Muscle (αSM) Actin (1A4) – Purified No Carrier Protein
Product No.: A460
- -
- -
Clone 1A4 Target α-Smooth Muscle Actin (SMA) Formats AvailableView All Product Type Monoclonal Antibody Isotype Mouse IgG2a k Applications FA , FC , IF , IHC , IHC FFPE , IP , WB |
- -
- -
Antibody DetailsProduct DetailsReactive Species Human/Mouse/Rat Immunogen N-terminal synthetic peptide corresponding to Human alpha smooth muscle actin. Product Concentration ≥1.0 mg/ml Purity ≥90% monomer by analytical SEC and SDS-Page Formulation This monoclonal antibody is aseptically packaged and formulated in 0.01 M phosphate buffered saline (150 mM NaCl) PBS pH 7.2 - 7.4 with no carrier protein, potassium, calcium or preservatives added. State of Matter Liquid Storage and Handling This antibody may be stored sterile as received at 2-8°C for up to one month. For longer term storage, aseptically aliquot in working volumes without diluting and store at -80°C. Avoid Repeated Freeze Thaw Cycles. Regulatory Status Research Use Only Country of Origin USA Shipping 2-8°C Wet Ice Additional Applications Reported In Literature ? FA IHC IF IP WB FC Each investigator should determine their own optimal working dilution for specific applications. See directions on lot specific datasheets, as information may periodically change. DescriptionDescriptionSpecificity Clone 1A4 activity is specific to alpha-smooth muscle actin (αSMA, SMA, smooth muscle aortic alpha‐actin (ACTA2)). Background Myofibroblasts are specialized connective tissue fibroblasts that use actin-based motors to generate contractile forces that are applied to extracellular matrix adhesion receptors 1. Alpha-smooth muscle actin (SMA) is a tissue specific actin isoform involved in myofibroblast differentiation, focal adhesion maturation, actin polymerization, tractional remodeling of the extracellular matrix, and the generation and transmission of mechanical forces in connective tissue, i.e., mechanotransduction. These physical forces are important for wound healing, joint and ligament remodeling due to injury or pregnancy, and the maintenance of tissue structure in the urinary bladder. SMA facilitates the generation of contractile forces in myofibroblasts and may contribute to scar formation and fibrocontractive diseases 1. Additionally, cancer-associated fibroblasts (CAF) play key roles in the tumor microenvironment, affecting tumor development, metabolism, and migration 2. SMA is highly expressed in CAFs and is widely used as a marker to identify CAF populations. However, SMA cannot be used for flow-sorting CAF populations for further functional studies because of its intracellular localization.
1A4 was produced using a synthetic decapeptide as immunogen, consisting of the NH2-terminal peptide of SMA coupled to BSA and a keyhole limpet hemocyanin (Ac-Glu(OBut)-Glu(OBut)-Glu(OBut)-Asp(OBut)-Ser(But)-Thr(But)-Ala-Leu-Val-Cys(Acm)-NHEt) 3. BALB/c mice were immunized and spleen cells were fused with Sp2/0 myeloma cells. Hybridomas were screened by ELISA against bovine aortic actin and further tested by immunofluorescence in chicken gizzard. Antigen Distribution Alpha-smooth muscle actin (SMA) is expressed by myofibroblasts and is the actin isoform typical of vascular smooth muscle cells. SMA is incorporated into stress fibers and focal adhesions and is also expressed by granulation tissue fibroblasts of healing wounds. Additionally, SMA expression is activated during the early stages of embryonic cardiovascular development. Astrocytes can also express SMA in culture. SMA is highly expressed in cancer-associated fibroblasts. Ligand/Receptor Myosins NCBI Gene Bank ID UniProt.org Research Area Cell Biology . Cell Motility/Cytoskeleton/Structure . Neuroscience References & Citations1. Wang J, Zohar R, McCulloch CA. Exp Cell Res. 312(3):205-214. 2006. 2. Nurmik M, Ullmann P, Rodriguez F, et al. Int J Cancer. 146(4):895-905. 2020. 3. Skalli O, Ropraz P, Trzeciak A, et al. J Cell Biol. 103(6 Pt 2):2787-2796. 1986. 4. Schürch W, Skalli O, Seemayer TA, et al. Am J Pathol. 128(1):91-103. 1987. 5. Rudy DE, Yatskievych TA, Antin PB, et al. Dev Dyn. 221(1):61-71. 2001. 6. Franke WW, Moll R. Differentiation. 36(2):145-163. 1987. 7. Chang CY, Chiou PP, Chen WJ, et al. Res Vet Sci. 88(2):285-293. 2010. 8. Lavaud S, Poirier B, Mandet C, et al. Am J Physiol Renal Physiol. 280(4):F683-694. 2001. 9. Li Y, Pan Z, Ji Y, et al. Eur Heart J. 23(7):567-573. 2002. 10. Cinel L, Düşmez D, Nabaei SH, et al. Acta Obstet Gynecol Scand. Technical ProtocolsCertificate of Analysis |
Formats Available
Products are for research use only. Not for use in diagnostic or therapeutic procedures.