Function
Key regulator of striated muscle performance by acting as the major Ca(2+) ATPase responsible for the reuptake of cytosolic Ca(2+) into the sarcoplasmic reticulum. Catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol to the sarcoplasmic reticulum lumen. Contributes to calcium sequestration involved in muscular excitation/contraction.
Biological Context
Subcellular Location: Endoplasmic reticulum membrane (Multi-pass membrane protein); Sarcoplasmic reticulum membrane (Multi-pass membrane protein)
Tissue Specificity: Skeletal muscle, fast twitch muscle (type II) fibers
Disease Association: Brody disease (BROD) : An autosomal recessive muscular disorder characterized by exercise-induced muscle stiffness and cramps primarily affecting the arms, legs, and eyelids, although more generalized muscle involvement may also occur. [The disease is caused by variants affecting the gene represented in this entry]
Product Specifications
Recombinant Human Sarcoplasmic/endoplasmic reticulum calcium ATPase 1 (ATP2A1), partial Protein is a recombinant protein from Homo sapiens (Human), expressed in in vitro E.coli expression system, covering amino acids 10-450aa, with N-terminal 10xHis-tagged tag, molecular weight 49.5kDa, purity Greater than 90% as determined by SDS-PAGE.. Suitable for ELISA and Western Blot applications.
