• Product NameRecombinant Human ATP2C1
• Brief DescriptionRecombinant Protein
• Immunogen DescriptionFusion protein corresponding to a region derived from 380-650 amino acids of human ATPase, Ca++ transporting, type 2C, member 1
• Target NameATPase, Ca++ transporting, type 2C, member 1
• Alternative Names    HHD; BCPM; PMR1; SPCA1; hSPCA1; ATP2C1A
• Accession No. Swissprot:P98194
  Gene Accession:BC028139
• UniprotP98194
• Gene ID27032;
• Storage -20~-80˚C, pH 7.6 PBS

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.

Note: For in vitro research use only, not for diagnostic or therapeutic use. This product is not a medical device.

• Flow Cytometry (FCM) General Protocol
• Immunofluorescence(IC)
• Immunohistochemistry(Polymer)
• Western Blotting