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:
1700121J11Rik, AT2C1, ATP dependent Ca(2+) pump PMR1, ATP-dependent Ca(2+) pump PMR1, ATP2C1, ATP2C1A, ATPase 2C1, ATPase Ca(2+) sequestering, ATPase Ca++ transporting type 2C member 1, AW061228, BCPM, Calcium transporting ATPase type 2C member 1, Calcium-transporting ATPase type 2C member 1, D930003G21Rik, HHD, hSPCA1, HUSSY 28, KIAA1347, MGC58010, MGC93231, OTTHUMP00000216066, OTTHUMP00000216068, OTTHUMP00000216069, OTTHUMP00000216071, OTTHUMP00000216072, OTTHUMP00000216073, OTTHUMP00000216074, OTTHUMP00000216075, PMR1, PMR1, rat, homolog of, PMR1L, Secretory pathway Ca(2+) ATPase 1, Secretory pathway Ca(2+)-transporting ATPase, Secretory pathway Ca2+/Mn2+ ATPase 1, SPCA, SPCA1

Immunogen: Recombinant protein of human ATP2C1

Swissprot: P98194
Gene Accession: BC028139

Purification Method: Affinity purification

Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4

Concentration: 0.9 mg/mL
Dilution: IHC 1:50-1:200

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

Alternative for product with catalog number:
sc-12647/sc-12650/sc-5548