You are viewing an incomplete version of our website. Please click to reload the website as full version.

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

Details for Product anti-ATP2C1 Antibody No. ABIN783438, Supplier: Log in to see
Antigen
  • ATP2C1
  • ATP2C1A
  • BCPM
  • HHD
  • PMR1
  • SPCA1
  • hSPCA1
  • Spca1
  • si:dkey-11p23.6
  • SPCA
  • 1700121J11Rik
  • AW061228
  • D930003G21Rik
  • pmr1
  • ATPase, Ca++ transporting, type 2C, member 1
  • ATPase, Ca++-sequestering
  • ATP2C1
  • atp2c1
  • Atp2c1
Alternatives
anti-Human ATP2C1 antibody for ELISA
Epitope
C-Term
18
9
8
7
5
3
2
1
1
1
Reactivity
Human, Mouse (Murine)
84
31
25
10
3
2
1
1
1
1
1
1
1
1
Host
Rabbit
63
21
Clonality
Polyclonal
Conjugate
This ATP2C1 antibody is un-conjugated
3
3
3
2
2
2
1
1
1
1
1
1
1
1
Application
Enzyme Immunoassay (EIA), Western Blotting (WB)
68
41
22
14
10
6
3
3
2
2
1
Options
Supplier
Log in to see
Supplier Product No.
Log in to see
Request

Get this product for free

It's quick and easy to submit your validation proposal. I want to validate this product

Learn more

Available images

Immunogen 19 amino acid peptide near the carboxy terminus of human ATP2C1
Specificity This antibody detects ATP2C1 (C-term). At least four isoforms of ATP2C1 are known to exist, this antibody will recognize only the three longest isoforms. ATP2C1 antibody will not cross-react with ATP2C2.
Cross-Reactivity (Details) Species reactivity (tested):Human, mouse
Purification Affinity chromatography purified via peptide column
Alternative Name ATP2C1 (ATP2C1 Antibody Abstract)
Background ATP2C1, also known as secretory pathway Ca2+/Mn2+-ATPase (SPCA) 1, 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 from the cytosol to the Golgi lumen. Defects in this gene cause Hailey-Hailey disease, an autosomal dominant disorder characterized by persistent blisters and erosions of the skin. Unlike the related protein ATP2C2, ATP2C1 is ubiquitously expressed and displays a lower maximal turnover rate for overall Ca2+-ATPase reaction and a higher apparent affinity for cytosolic Ca2+ activation of phosphorylation. Recent evidence suggests that ATP2C1 is a key regulator of insulin-like growth factor receptor (IGF1R) processing in tumor progression in basal breast cancers.Synonyms: ATP-dependent Calcium pump PMR1, ATPase 2C1, Calcium-transporting ATPase type 2C member 1, HUSSY-28, KIAA1347, PMR1L
Gene ID 27032
NCBI Accession NP_001001485
UniProt P98194
Research Area Signaling, Metabolism, Enzymes
Pathways Transition Metal Ion Homeostasis, Ribonucleoside Biosynthetic Process
Application Notes Optimal working dilution should be determined by the investigator.
Restrictions For Research Use only
Buffer PBS containing 0.02 % sodium azide
Preservative Sodium azide
Precaution of Use This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Handling Advice Avoid repeated freezing and thawing.
Storage 4 °C/-20 °C
Storage Comment Store at 2 - 8 °C for up to one month or (in aliquots) at -20 °C for longer.
Supplier Images
Western Blotting (WB) image for anti-ATP2C1 antibody (ATPase, Ca++ Transporting, Type 2C, Member 1) (C-Term) (ABIN783438) Western blot analysis of ATP2C1 in mouse brain tissue lysate with ATP2C1 antibody at ...
Background publications Grice, Vetter, Faddy, Kenny, Roberts-Thomson, Monteith: "Golgi calcium pump secretory pathway calcium ATPase 1 (SPCA1) is a key regulator of insulin-like growth factor receptor (IGF1R) processing in the basal-like breast cancer cell line MDA-MB-231." in: The Journal of biological chemistry, Vol. 285, Issue 48, pp. 37458-66, 2010 (PubMed).

Dode, Andersen, Vanoevelen, Raeymaekers, Missiaen, Vilsen, Wuytack: "Dissection of the functional differences between human secretory pathway Ca2+/Mn2+-ATPase (SPCA) 1 and 2 isoenzymes by steady-state and transient kinetic analyses." in: The Journal of biological chemistry, Vol. 281, Issue 6, pp. 3182-9, 2006 (PubMed).

Hu, Bonifas, Beech, Bench, Shigihara, Ogawa, Ikeda, Mauro, Epstein: "Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease." in: Nature genetics, Vol. 24, Issue 1, pp. 61-5, 2000 (PubMed).