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The protein encoded by ATP2C1 belongs to the family of P-type cation transport ATPases. Additionally we are shipping ATP2C1 Proteins (7) and ATP2C1 Kits (1) and many more products for this protein.
Showing 10 out of 86 products:
Human Polyclonal ATP2C1 Primary Antibody for EIA, WB - ABIN783438
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 2006
Show all 3 references for ABIN783438
Human Monoclonal ATP2C1 Primary Antibody for IHC, ELISA - ABIN1724719
Majore, Biolcati, Barboni, Cannistraci, Binni, Crisi, Picardo, Grammatico: ATP2C1 gene mutation analysis in Italian patients with Hailey-Hailey disease. in The Journal of investigative dermatology 2005
Show all 2 references for ABIN1724719
Human Monoclonal ATP2C1 Primary Antibody for IF, IP - ABIN565309
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 2010
Show all 2 references for ABIN565309
Human Monoclonal ATP2C1 Primary Antibody for IHC, WB - ABIN2869472
Yokota, Sawamura: Hailey-Hailey disease with affective disorder: report of a case with novel ATP2C1 gene mutation. in Journal of dermatological science 2006
Chicken Polyclonal ATP2C1 Primary Antibody for WB - ABIN2781847
Li, Peng, Xiao, Wang, Liu, Pan, Zhou, Luo: A novel deletion mutation of the ATP2C1 gene in Chinese patients with Hailey-Hailey disease. in Journal of the European Academy of Dermatology and Venereology : JEADV 2008
Two novel ATP2C1 mutations have been found in two unrelated Chinese patients with Hailey-Hailey disease pedigree.
Besides the level of functional ATP2C1 protein, levels of other ATPase (show DNAH8 Antibodies) proteins may influence expressivity of the disease and may also contribute to atypical presentations in three male members of the Hailey Hailey disease family.
This is the first genetic report of HHD from Lebanon in which we identified three novel mutations in ATP2C1 and shed light on the molecular mechanisms and pathogenesis of HHD by linking stress signals like heat shock to the observed phenotypes
We speculate that a novel pathogenic mechanism involving SPCA1, p63 (show RPE65 Antibodies), and IRF6 (show IRF6 Antibodies) may play a role in the skin lesions occurring in HHD.
Data suggest that calcium ATPase (show CA-P60A Antibodies) ATP2C1 gene expression is influenced by an overlapping protein asteroid homolog 1 ASTE1 (show ASTE1 Antibodies) gene.
The CFL-1 (show VPS72 Antibodies)-dependent recruitment of actin to SPCA1 following calcium influx is critical for secretory cargo sorting.
Case Report: haploinsufficiency of ATP2C1 mutations is the causative mechanism of Hailey-Hailey disease.
We report sibling cases of Hailey-Hailey disease with novel mutations in the ATP2C1 gene that showed unique and atypical clinical phenotypes mimicking seborrheic dermatitis, pemphigus vulgaris (show DSG3 Antibodies), or pemphigus foliaceus (show DSG1 Antibodies)
A novel mutation is identified in ATP2C1 linked to Chinese patients with Hailey-Hailey disease.
we report four novel mutations of the ATP2C1 gene involved in HHD, expanding the repertoire of ATP2C1 mutations underlying HHD.
The timing, magnitude of TMEM165 (show TMEM165 Antibodies) expression and its Golgi location supports a role for this Golgi Ca2 (show CA2 Antibodies)+/H+ antiporter as a contributor to mammary Golgi calcium transport needs, in addition to the better-characterized roles of SPCA 1 and 2.
loss of the Golgi Ca(2 (show CA2 Antibodies)+) pump causes Golgi stress, expansion of the Golgi, increased apoptosis, and embryonic lethality and demonstrates that SPCA1 haploinsufficiency causes a genetic predisposition to cancer.
The synthesized siPMR1 can significantly silence the expression of PMR1 and promote the secretion of insulin (show INS Antibodies) in the islet cells in vitro.
Impaired cellular divalent calcium ion Ca2 (show CA2 Antibodies)+ homeostasis and/or the altered targeting of organellar proteins under conditions of SPCA1 knockdown highlight the importance of SPCA1 function for normal neural differentiation.
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.
ATPase, Ca++ transporting, type 2C, member 1
, ATPase 2C1
, Calcium-transporting ATPase type 2C member 1
, calcium-transporting ATPase type 2C member 1-like
, ATP-dependent Ca(2+) pump PMR1
, ATPase, Ca(2+)-sequestering
, calcium-transporting ATPase type 2C member 1
, secretory pathway Ca2+/Mn2+ ATPase 1
, ATPase, Ca++-sequestering
, calcium-transporting ATPase 2C1
, secretory pathway Ca(2+)-ATPase 1
, secretory pathway Ca(2+)-transporting ATPase