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Human Cholecystokinin Kit ELISA pour Competition ELISA - ABIN1979281
Gurda, Guo, Lee, Molkentin, Williams: Cholecystokinin activates pancreatic calcineurin-NFAT signaling in vitro and in vivo. dans Molecular biology of the cell 2008
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Guinea Pig Cholecystokinin Kit ELISA pour Competition ELISA - ABIN1383607
Pagani, Pranzo, Galante: [Determination of cholylglycine in alcoholic hepatopathies. Clinical usefulness]. dans Minerva dietologica e gastroenterologica 1985
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Rat (Rattus) Cholecystokinin Kit ELISA pour Sandwich ELISA - ABIN368055
Duraisamy, Bayen, Saini, Sharma, Vats, Singh: Changes in ghrelin, CCK, GLP-1, and peroxisome proliferator-activated receptors in a hypoxia-induced anorexia rat model. dans Endokrynologia Polska 2015
Human Cholecystokinin Kit ELISA pour Competition ELISA - ABIN415079
Biberoglu, Kirbas, Iskender, Dirican, Daglar, Demirtas, Doganay, Uygur, Biberoglu: Disturbed release of cholecystokinin in pregnant women with hyperemesis gravidarum. dans The journal of obstetrics and gynaecology research 2015
The CCK polymorphism have reported significant association of -45C>T polymorphism with the presence of hallucinations.
CCK does not appear to play a unique independent role in satiety/satiation.
CCK release has been found to be halved in pregnant women with hyperemesis gravidarium, which supports the hypothesis that gastrointestinal motility is increased in pregnant women with hyperemesis gravidarium.
CCK in plasma is an independent marker of cardiovascular mortality in elderly female patients.
These data offer preliminary evidence supporting an association between the rs1799923 polymorphism in the CCK gene and PTSD
Data suggest that endocrine responses differ between jejunal and gastric enteral feeding, with higher peak plasma CCK (cholecystokinin), PYY (peptide YY), and GLP-1/2 (glucagon-like peptides 1/2) concentrations being attained after jejunal feeding.
active GLP-1 (Montrer GCG Kits ELISA) produced in the islet stimulates cholecystokinin production and secretion in a paracrine manner via cyclic AMP (Montrer APRT Kits ELISA) and CREB (Montrer CREB1 Kits ELISA).
Cardiac expression of pro-cholecystokinin is cell-specific, which differentiates the expression from that of intestinal endocrine cells and cerebral neurons. Plasma Pro-CCK is a prognostic marker in patients with stable heart failure.
CCK binding modulates the contractile function of the lower esophageal sphincter through differential binding to the CCK-A receptor (Montrer CCKAR Kits ELISA) on the sling and clasp (Montrer CLASRP Kits ELISA) fibers
Data suggest that up-regulation of plasma CCK levels is 50% higher following breakfast of meal replacement beverage containing fat emulsion of rapeseed oil with droplet size of 0.1 um (versus 0.3 um); satiety response and food intake are unaffected.
These studies reemphasize the beneficial effects imparted by co-administration of obestatin and CCK8 and their potential use towards countering obesity.
that Rip2 modifies VEGF-induced signalling and vascular permeability in myocardial ischaemia
new information on the cell specific localization of NUCB2/nesfatin-1 (Montrer NUCB2 Kits ELISA) in the intestinal mucosa, and a novel function for nesfatin-1 (Montrer NUCB2 Kits ELISA) in modulating intestinal CCK and PYY expression and secretion
Results showed that CCK is important for lipid transport and energy expenditure to control body weight in response to dietary lipid feeding
SP1 (Montrer SP1 Kits ELISA) results in a CCK response deficiency that may contribute to the increased meal size and overall hyperphagia in synphillin-1 transgenic mice
serves as a novel positive modulator of ventricular remodelling after myocardial infarction via the regulation of NF-kappaB (Montrer NFKB1 Kits ELISA) and p38 (Montrer CRK Kits ELISA) signalling
active GLP-1 (Montrer GCG Kits ELISA) produced in the islet stimulates cholecystokinin production and secretion in a paracrine manner via cyclic AMP (Montrer TMPRSS5 Kits ELISA) and CREB (Montrer CREB1 Kits ELISA).
Data (including data from studies using transgenic mice) suggest that enhanced Cck expression in pancreatic beta-cells protects these cells from the cell-withering effects of aging, apoptotic stress, and (streptozotocin-induced) diabetes type 2.
Deoxynivalenol induced cholecystokinin and glucagon-like peptide 1 (Montrer GCG Kits ELISA) release by enteroendocrine cells in mediated by casR (Montrer CASR Kits ELISA)/TRPA1 (Montrer TRPA1 Kits ELISA) signaling.
Bacterial polysaccharide-responsive miR (Montrer MLXIP Kits ELISA)-150 and miR (Montrer MLXIP Kits ELISA)-143 RIPK2 (Montrer RIPK2 Kits ELISA) and TAK1 (Montrer NR2C2 Kits ELISA) to suppress NOD2 (Montrer NOD2 Kits ELISA)-induced immunomodulators.
We conclude that only a small fraction of neuronal CCK is nonsulfated. The intracellular distribution of nonsulfated CCK in neurons suggests that they contribute only modestly to the CCK transmitter activity.
Cardiac expression of pro-cholecystokinin is cell-specific, which differentiates the expression from that of intestinal endocrine cells and cerebral neurons.
This review explores the role of luminal cholecystokinin on the regulation of exocrine pancreatic secretion in author's studies of neonatal pigs.
This review explores the role of luminal cholecystokinin on the regulation of exocrine pancreatic secretion in author's studies of newborn calves.
Cholecystokinin is a brain/gut peptide. In the gut, it induces the release of pancreatic enzymes and the contraction of the gallbladder. In the brain, its physiologic role is unclear. The cholecystokinin pro-hormone is processed by endo- and exo-proteolytic cleavages. Two transcript variants encoding the same protein have been found for this gene.
, cholecystokinin triacontatriapeptide
, receptor-interacting serine/threonine-protein kinase 2
, tyrosine-protein kinase RIPK2