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.
仕様
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
Host：Rabbit
Reactivity：Human,Mouse,Rat
Applications：WB,IHC
Concentration：1mg/ml
Immunogen：Recombinant protein of human ATP2C1
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：Buffer： PBS with 0.02％ sodium azide, 50％ glycerol, pH7.3.
Dilution：WB1：500 - 1：2000 IHC1：50 - 1：200
Gene_ID（human）：27032
Swissprot：P98194
Isotype：IgG
Research Areas：Cancer, Metabolism, Signal transduction
