Anti-Human/Mouse/Rat ATP2C1 Polyclonal Antibody

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.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA12550
Size 100μl
Host Type Rabbit
Immunogen Recombinant protein of human ATP2C1
Specificity Found in most tissues except colon, thymus, spleen and leukocytes. Most abundant in keratinocytes and kidney.
Isotype IgG
Reacitivity Human,Mouse,Rat
Clone
Uniprot P98194
Concentration 0.9 mg/mL
Dilution IHC 1:50-1:200
Formulation
Application IHC,ELISA
Other Names 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
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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