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Antibody
Catalog #:

SG-0189R

Product Name : Rabbit Anti-alpha smooth muscle Actin Polyclonal Antibody
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Applications : WB(1:500-2000) ELISA(1:500-1000) Flow-Cyt(1μg /test) Not yet tested in other applications.  Optimal working dilutions must be determined by the end user.
Reactivity : Reacts with:Human,Mouse,Rat,Chicken,Dog,Pig,Cow,Rabbit,Sheep,Fish,Guinea Pig,Hamster,Cat,HMt,Op
Conjugation : KLH conjugated synthetic peptide derived from human Actin alpha:301-375/375
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Source : Rabbit
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Concentration : 1mg/ml
Purification : affinity purified by Protein A
Storage : Store at -20℃ (Avoid repeated freeze/thaw cycles).
Synonyms : alpha sarcomeric Actin; alpha smooth muscle Actin; Actin alpha; ASMA; ASM-A; alpha-SMA; alpha SMA; AAT6; ACTA2; Actin alpha 2 smooth muscle aorta; Actin aortic smooth muscle; ACTSA; ACTVS; Alpha 2 actin; Alpha-actin 2; Cell growth inhibiting gene 46 protein; Growth inhibiting gene 46; ACTA_HUMAN; Actin alpha 2 smooth muscle aorta; Actin aortic smooth muscle; Actin, aortic smooth muscle; Alpha 2 actin; Alpha actin 2; Alpha cardiac actin; Alpha-actin 2; Alpha-actin-2; Cell growth inhibiting gene 46 protein; Cell growth-inhibiting gene 46 protein; Growth inhibiting gene 46; MYMY5  α-Smooth Muscle Actin; α Smooth Muscle Actin;
Background : 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.
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