Recombinant Human ATP2C1 cell lysate

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Recombinant Human ATP2C1 cell lysate

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Cat.No. : ATP2C1-148HCL
Description : 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 the calcium. Defects in this gene cause Hailey-Hailey disease, an autosomal dominant disorder. Alternatively spliced transcript variants encoding different isoforms have been identified.
Species : Human
Size : 100 ul
Storage Buffer : 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
Applications : Western Blot;
Gene Name : ATP2C1 ATPase, Ca++ transporting, type 2C, member 1 [ Homo sapiens ]
Official Symbol : ATP2C1
Synonyms : ATP2C1; ATPase, Ca++ transporting, type 2C, member 1; BCPM, benign chronic pemphigus (Hailey Hailey disease); calcium-transporting ATPase type 2C member 1; ATP2C1A; KIAA1347; PMR1; secretory pathway Ca2+/Mn2+ ATPase 1; SPCA1; HUSSY-28; ATPase 2C1; ATPase, Ca(2+)-sequestering; ATP-dependent Ca(2+) pump PMR1; HHD; BCPM; hSPCA1;
Gene ID : 27032
mRNA Refseq : NM_001001485
Protein Refseq : NP_001001485
MIM : 604384
UniProt ID : P98194
Chromosome Location : 3q21.3
Pathway : Ion channel transport, organism-specific biosystem; Ion transport by P-type ATPases, organism-specific biosystem; Transmembrane transport of small molecules, organism-specific biosystem; calcium transport I, organism-specific biosystem;
Function : ATP binding; ATP binding; calcium ion binding; calcium-transporting ATPase activity; NOT calcium-transporting ATPase activity; calcium-transporting ATPase activity; calcium-transporting ATPase activity; hydrolase activity; hydrolase activity, acting on acid anhydrides, catalyzing transmembrane movement of substances; manganese ion binding; manganese-transporting ATPase activity; metal ion binding; nucleotide binding; signal transducer activity;

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