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The protein encoded by PCSK1 belongs to the subtilisin-like proprotein convertase family. Additionally we are shipping PCSK1 Antibodies (30) and PCSK1 Kits (6) and many more products for this protein.
Showing 7 out of 7 products:
Human PCSK1 Protein expressed in Human Cells - ABIN2002138
Jackson, Creemers, Farooqi, Raffin-Sanson, Varro, Dockray, Holst, Brubaker, Corvol, Polonsky, Ostrega, Becker, Bertagna, Hutton, White, Dattani, Hussain, Middleton, Nicole, Milla, Lindley, ORahilly: Small-intestinal dysfunction accompanies the complex endocrinopathy of human proprotein convertase 1 deficiency. in The Journal of clinical investigation 2003
Show all 4 references for ABIN2002138
Pcsk1 has been sequenced and characterized.
these common variants in PCSK1 and POMC (show POMC Proteins) were not the major cause of obesity in the Thai subjects sampled. However, variants in PCSK1 did affect cholesterol level, LDL-C level, and waist circumference.
we demonstrate evidence that common gene variation in PCSK1 contributes to BMI variation and susceptibility to common obesity in the largest known meta-analysis published to date in genetic epidemiology.
Data show that prohormone convertase 1/3 (PC1/3) endoplasmic reticulum-retained mutants induce endoplasmic reticulum stress.
Mechanism of Fine-tuning pH Sensors in Proprotein Convertases: IDENTIFICATION OF A pH-SENSING HISTIDINE PAIR IN THE PROPEPTIDE OF PROPROTEIN CONVERTASE 1/3.
We showed for the first time that a nonsense mutation in PCSK1 was likely to cause dominantly inherited human obesity, due to the inhibiting properties of the propeptide fragment encoded by the null allele
Epistases between single nucleotide polymorphisms within proprotein convertase subtilisin/kexin type 1(PCSK1) and dopamine beta-hydroxylase(DBH (show DBH Proteins)) genes are significantly associated with susceptibility or resistance to premature ovarian failure
FTO (show FTO Proteins)-rs9939609, TMEM18 (show TMM18 Proteins)-rs6548238 and PCSK1-rs6234 polymorphisms are significantly associated with body mass index in a southern Chinese population.
Common genetic variants in PCSK1 are associated with coronary artery disease in Chinese patients with type 2 diabetes.
PC1/3(S357G) exhibited a lower calcium dependence; a higher pH optimum.
PCSK1 is overexpressed in fibrolamellar hepatocellular carcinoma.
Prohormone convertase PC1 expression is up-regulated in a cell-specific manner in bovine neuroendocrine ocular ciliary epithelium.
a model of the membrane topology of the prohomone convertase PC3, where it is anchored to lipid rafts in secretory granule membranes via the transmembrane domain
PC1 and PC2 (show CBX4 Proteins) are involved in the C-terminal processing of protachykinin peptides and suggest a major role in the maturation of the protachykinin-1 (show TAC1 Proteins) protein
Binding of MAGP2 (show MFAP5 Proteins) to microfibrils is regulated by proprotein convertase cleavage.
Data indicate that the mutant PC1/3-N222D protein coimmunoprecipitates with wildtype(WT) prohormone convertase 1/3 (PC1/3) and exerts a modest effect on intracellular retention of the WT enzyme.
proSAAS (show PCSK1N Proteins) as a novel down-regulated target of Pax6 (show PAX6 Proteins)
Loss of PC1 in mice showed a dramatic decrease in the biosynthesis of all proTRH-derived peptides analyzed including TRH (show TRH Proteins) and its immediate precursor TRH (show TRH Proteins)-Gly.
PC1/3 also has an important role in the regulation of the innate immune system, most likely through the regulation of cytokine secretion in macrophages.
Reports demonstrate that mouse proprotein convertase 1/3 (mPC1 (show BRP44L Proteins)/3) has a lag (show STMN1 Proteins) phase of activation by substrates that can be interpreted as a hysteretic behavior of the enzyme for their hydrolysis.
Intraislet production of GLP-1 (show GCG Proteins) by activation of prohormone convertase 1/3 in pancreatic alpha-cells in mouse models of ss-cell regeneration.
Data suggest that PC1/3 and many convertase-specific properties are attributable less to convertase-specific catalytic cleft residues than to convertase-specific domain interactions.
These results demonstrate a prominent role for cathepsin L (show CTSL1 Proteins), jointly with PC1/3 and PC2 (show CBX4 Proteins), for production of dynorphins in brain.
Study identified 14 polymorphisms that were organized in nine haplotypes, clearly distributed in two clades of putative European and Asian origin and showed that the porcine PCSK1 gene is associated with fat deposition.
The protein encoded by this gene belongs to the subtilisin-like proprotein convertase family. The members of this family are proprotein convertases that process latent precursor proteins into their biologically active products. This encoded protein is a type I proinsulin-processing enzyme that plays a key role in regulating insulin biosynthesis. It is also known to cleave proopiomelanocortin, prorenin, proenkephalin, prodynorphin, prosomatostatin and progastrin. Mutations in this gene are thought to cause obesity. This encoded protein is associated with carcinoid tumors. Mutations in this gene have been associated with susceptibility to obesity and proprotein convertase 1/3 deficiency. Multiple transcript variants encoding different isoforms have been found for this gene.
neuroendocrine convertase 1
, prohormone convertase 1
, NEC 1
, prohormone convertase 3
, Protein convertase subtilisin / kexin type I
, Protein convertase subtilisin / kexin, type I
, proprotein convertase 1
, furin homolog
, prohormone convertase 1/3
, propeptide-processing protease
, prohormone convertase