ATP2C1 Polyclonal Antibody

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.

Research Area: Cancer, Metabolism, Signal Transduction

Synonyms:
ATP2C1, ATP2C1A, BCPM, HHD, PMR1, SPCA1, hSPCA1

Immunogen: Recombinant fusion protein of human ATP2C1 (NP_001186114.1).

Swissprot: P98194
Gene ID: 27032

Purification Method: Affinity purification

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

Concentration: 1 mg/mL
Dilution: IHC 1:50-1:200

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