兔抗ATP2C1多克隆抗体

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.

Applications:

ELISA, IHC

Name of antibody:

ATP2C1

Immunogen:

Fusion protein of human ATP2C1

Full name:

ATPase, Ca++ transporting, type 2C, member 1

Synonyms：

HHD; BCPM; PMR1; SPCA1; hSPCA1; ATP2C1A

SwissProt:

P98194

ELISA Recommended dilution:

1000-5000

IHC positive control:

Human brain and human prostate cancer

IHC Recommend dilution:

50-200