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Reconstitute with 0.2 mL of distilled water to yield a concentration of 500 µg/mL.
Positive Control - WB: human placenta tissue, human Hela whole cell, human HepG2 whole cell, human 293T whole cell, human A431 whole cell, human U87 whole cell, human U937 whole cell, human K562 whole cell, rat heart tissue, rat brain tissue, rat kidney tissue, mouse heart tissue, mouse brain tissue, mouse spleen tissue, mouse kidney tissue. IHC: human breast cancer tissue, human colorectal adenocarcinoma tissue, human placenta tissue, human tonsil tissue, mouse heart tissue, rat heart tissue.
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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: actin alpha 1; Actin, alpha skeletal muscle; Alpha-actin-1; nemaline myopathy type 3
基因别名: AA959943; ACTA; Acta-2; ACTA1; Acts; Actsk-1; ASMA; CFTD; CFTD1; CFTDM; MPFD; NEM1; NEM2; NEM3; SHPM
UniProt ID: (Human) P68133, (Mouse) P68134, (Rat) P68136
Entrez Gene ID: (Human) 58, (Mouse) 11459, (Rat) 29437