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Pcsk1 has been sequenced and characterized.
findings suggest that the major neuroendocrine features of Prader-Willi syndrome are due to PC1 deficiency
PCSK1 mutations are associated with Obesity.
PCSK1 expression is significantly upregulated in human masticatory mucosa during wound healing
these common variants in PCSK1 and POMC (show POMC ELISA Kits) 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 ELISA Kits)) genes are significantly associated with susceptibility or resistance to premature ovarian failure
FTO (show FTO ELISA Kits)-rs9939609, TMEM18 (show TMM18 ELISA Kits)-rs6548238 and PCSK1-rs6234 polymorphisms are significantly associated with body mass index in a southern Chinese population.
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
These pathways are consistent with previously reported behavioral and biochemical phenotypes that typify mice lacking ENT1 (show SLC29A1 ELISA Kits). Moreover, we validated decreased expression of the SNARE (show VTI1B ELISA Kits) complex protein VAMP1 (synaptobrevin-1 (show VAMP1 ELISA Kits)) in the dHip as well as decreased expression of pro-dynorphin (PDYN (show PDYN ELISA Kits)), neuroendocrine convertase (PCSK1), and Leu-Enkephalin (dynorphin-A (show PDYN ELISA Kits)) in the nucleus accumbens
macrophages from PC1/3 KO mice and rat PC1/3-KD NR8383 macrophages secreted more pro-inflammatory cytokines such as TNF-alpha (show TNF ELISA Kits), IL6 (show IL6 ELISA Kits), IL1alpha (show IL1A ELISA Kits) and CXCL2 (show CXCL2 ELISA Kits).
PC1 and PC2 are involved in the C-terminal processing of protachykinin peptides and suggest a major role in the maturation of the protachykinin-1 (show TAC1 ELISA Kits) protein
Binding of MAGP2 (show MFAP5 ELISA Kits) 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 ELISA Kits) as a novel down-regulated target of Pax6 (show PAX6 ELISA Kits)
Loss of PC1 in mice showed a dramatic decrease in the biosynthesis of all proTRH-derived peptides analyzed including TRH (show TRH ELISA Kits) and its immediate precursor TRH (show TRH ELISA Kits)-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 ELISA Kits)/3) has a lag (show STMN1 ELISA Kits) phase of activation by substrates that can be interpreted as a hysteretic behavior of the enzyme for their hydrolysis.
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