Product Name	Recombinant Rabbit Anti-ACTA1 Monoclonal Antibody
Cat No.	SLA0791M
Alias	ACTA; ASMA; CFTD; CFTD1; CFTDM; CMYO2A; CMYO2B; CMYO2C; CMYP2A; CMYP2B; CMYP2C; MPFD; NEM1; NEM2; NEM3; SHPM; Acta-2; Acts; Actsk-1; ACTS_CHICK; ACTA1; Alpha-actin-1; 3.6.4.-; ACTS_BOVIN; ACTS_HUMAN; ACTS_MOUSE; ACTS_PIG; ACTS_RABIT; ACTS_RAT; actin alpha 1, skeletal muscle; nemaline myopathy type 3
Host Species	Mouse
Isotype	IgG1/Kappa
Clonality	Monoclonal
Clone No.	7C8
React Species	Human,Mouse,Rat,Pig,Chicken,Bovine
Applications	WB (1:500-2000) IHC-P (1:100-500) IHC-F (1:100-500) IF (1:100-500) ELISA (1:5000-10000) Not yet tested in other applications. Optimal working dilutions must be determined by the end user.
Immunogen	Synthesized peptide derived from human Actin, sarcomeric muscle
Purification	affinity purified by Protein G
Concentration	1mg/ml
Predicted MW.	42 kDa
Swiss-Prot	P68133
Storage	0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
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. [provided by RefSeq , Jul 2008]
Attention	This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

 

FOR RESEARCH USE ONLY. Not for use in diagnostic or therapeutic procedures.