ATPase, Ca++ Transporting, Type 2C, Member 1 (ATP2C1) antibody

Details for Product No. ABIN361612
Request Want additional data for this product?

The Independent Validation Initiative strives to provide you with high quality data. Find out more

Antigen
Synonyms ATP2C1, ATP2C1A, BCPM, HHD, PMR1, SPCA1, hSPCA1, Spca1, si:dkey-11p23.6, SPCA, 1700121J11Rik, AW061228, D930003G21Rik, pmr1
Reactivity
Human
(52), (15), (8), (7), (1), (1), (1), (1), (1)
Host
Mouse
(38), (14)
Clonality
Polyclonal
Conjugate
Un-conjugated
(1), (1), (1), (1), (1), (1)
Application
Western Blotting (WB), Immunofluorescence (IF)
(51), (31), (17), (4), (3), (2), (2), (1), (1), (1)
Pubmed 3 references available
Quantity 50 μg
Shipping to United States (Change)
Availability Will be delivered in 9 to 11 Business Days
Request Want additional data for this product?

The Independent Validation Initiative strives to provide you with high quality data. Find out more

Catalog No. ABIN361612
627.13 $
Plus shipping costs $45.00

Order hotline:

  • +1 404 474 4654
  • +1 888 205 9894 (TF)
Immunogen Recombinant protein of full length Human ATP2C1
Purification Protein A purified
Alternative Name ATP2C1
Background Function: This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of the calcium Subcellular location: Golgi apparatus membrane, Multi-pass membrane protein Tissue specificity: Found in most tissues except colon, thymus, spleen and leukocytes. Most abundant in keratinocytes and kidney Sequence similarities: Belongs to the cation transport ATPase (P-type) family.
Gene ID 27032
Research Area Enzymes
Application Notes WB: 1ug/ml. IF: 10ug/ml
Restrictions For Research Use only
Concentration 0.5 mg/ml
Buffer PBS, pH 7.2
Storage -20 °C
General Hu, Bonifas, Beech et al.: "Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease." in: Nature genetics, Vol. 24, Issue 1, pp. 61-5, 2000 (PubMed).

Sudbrak, Brown, Dobson-Stone et al.: "Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pump." in: Human molecular genetics, Vol. 9, Issue 7, pp. 1131-40, 2000 (PubMed).

Fairclough, Dode, Vanoevelen et al.: "Effect of Hailey-Hailey Disease mutations on the function of a new variant of human secretory pathway Ca2+/Mn2+-ATPase (hSPCA1)." in: The Journal of biological chemistry, Vol. 278, Issue 27, pp. 24721-30, 2003 (PubMed).

Validation Images
Did you look for something else?
back to top