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Also for ACTA1 (NM_001100)
|Recombinant protein fragment contain a sequence corresponding to a region within amino acids 1 and 129 of Human ACTA1|
|0.1M Tris, 0.1M Glycine, 10% Glycerol (pH7). 0.01% Thimerosal was added as a preservative.|
|Purified by antigen-affinity chromatography. (Protein A or G Sepharose)
|Homo sapiens actin, alpha 1, skeletal muscle (ACTA1)|
|ACTA; ASMA; CFTD; CFTD1; CFTDM; MPFD; NEM1; NEM2; NEM3|
|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]|
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Sample(30 ug of whole cell lysate) A:Raji (anti-ACTA1 antibody diluted at 1:1000)
Immunohistochemical analysis of paraffin-embedded Skeletal Muscle , using alpha Actin (skeletal muscle)(anti-ACTA1 antibody) antibody(10 ?g/ml).