This gene encodes one of the SERCA Ca(2+)-ATPases, which are intracellular pumps located in the sarcoplasmic or endoplasmic reticula of muscle cells. This enzyme catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol to the sarcoplasmic reticulum lumen, and is involved in muscular excitation and contraction. Mutations in this gene cause some autosomal recessive forms of Brody disease, characterized by increasing impairment of muscular relaxation during exercise. Alternative splicing results in three transcript variants encoding different isoforms.

Aliases :   ATP2A; SERCA1    

Entrez GeneID :   487    

Swissprot:   O14983        

WB Predicted band size:    110kDa    

Host/Isotype :   Mouse IgG1    

Species Reactivity :   Human,Mouse,Monkey    

Immunogen :   Purified recombinant fragment of human ATP2A1 (AA: 487-631) expressed in E. Coli.    

FCM    1/200 - 1/400    

ELISA    1/10000