ATP2C1 polyclonal, anti-human, mouse, rat

Background:
The protein encoded by this gene belongs to the family of P-type cation transport ATPases. This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of calcium ions. Defects in this gene cause Hailey-Hailey disease, an autosomal dominant disorder. Alternatively spliced transcript variants encoding different isoforms have been identified.

Synonyms: ATP2C1A, BCPM, HHD, PMR1, SPCA1, hSPCA1

Cellular Location: Golgi apparatus membrane Multi-pass membrane protein

Immunogen:
Recombinant protein of human ATP2C1

Gene Symbol: ATP2C1

Gene ID: 27032

Swiss prot: P98194

Calculated MW: 101kDa

Recommended dilution:
WB 1:500-2000, IHC 1:50-200,

Purity:
Affinity purification

Storage Buffer:
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

Storage:
Store at -20℃. Avoid freeze / thaw cycles.