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Human Vip Protein expressed in Human Cells - ABIN2005717
Kulick, Chaiseha, Kang, Rozenboim, El Halawani: The relative importance of vasoactive intestinal peptide and peptide histidine isoleucine as physiological regulators of prolactin in the domestic turkey. in General and comparative endocrinology 2005
VIP and CRF (show CRH Proteins) reduce ADAMTS (show ADAMTS13 Proteins) expression and function in osteoarthritis synovial fibroblasts.
a differential effect of VIP on the expression of TNFalpha (show TNF Proteins) and IL-6 (show IL6 Proteins) receptors, since VIP was only able to decreased expression in LPS (show IRF6 Proteins)-stimulated monocytes but not in 4/74-infected monocytes.
VIP promotes Th17 polarization of memory Th cells in early arthritis.
The circadian rhythm amplitude of motor activity in both Alzheimer disease subjects and age-matched controls is correlated with the number of vasoactive intestinal peptide-expressing suprachiasmatic nucleus neurons.
Skin VIP expression, a marker of sudomotor innervation, was significantly lower in patients with familial transthyretin (show TTR Proteins) amyloid neuropathy compared to controls.
Alterations in VIP expression may play a role in irritable bowel syndrome.
Interictal CGRP (show S100A12 Proteins) and, to a lesser degree, VIP levels measured in peripheral blood are of great help in predicting response of chronic migraine patients to Onabotulinumtoxin type A
The antimicrobial peptide, VIP is a neuropeptide with activity against a range of microorganisms from skin, oral, respiratory and gastrointestinal tract sites.
VIP is significantly increased in the patients with chronic obstructive pulmonary disease and pulmonary hypertension.
Serum levels of vasoactive intestinal peptide as a prognostic marker in early arthritis.
High level of co-expression of PACAP (show ADCYAP1 Proteins) with VIP, SP and CGRP (show CALCA Proteins) in the distal ganglia of the vagus sensory perikarya directly implicates studied peptides in their functional interaction during nociceptive vagal transduction.
The present study reports for the first time on the co-localisation of CART and VIP in myenteric neurons of the porcine transverse colon.
Data show that PKA and PKC pathways are involved in the differential regulation of production of the neuropeptides (Met)enkephalin, galanin (show GAL Proteins), somatostatin (show SST Proteins), NPY (show NPY Proteins), and VIP.
The intestinal concentration of VIP increased gradually during development. The levels of VIP and VIPR1 (show VIPR1 Proteins) in liver gradually decreased during development.
in cortical VIP neurons, experience-dependent gene transcription regulates visual acuity by activating the expression of IGF1 (show IGF1 Proteins), thus promoting the inhibition of disinhibitory neurons and affecting inhibition onto cortical pyramidal neurons
Chronic loss of VIP in mice leads to a disruption of certain but not all immunological compartments.
neuropeptides CGRP (show CALCA Proteins) and VIP have an important role in suppressing bone resorptive activities through RANKL/OPG (show TNFSF11 Proteins) pathway, similar to mechanical loading.
The results show in vivo a primary role for VIP chronic exposure in CFTR (show CFTR Proteins) membrane stability and function and confirm in vitro data.
VIP signaling modulates the output from the olfactory bulb to maintain circadian rhythms in the mammalian olfactory system.
VIP neuropeptide-mediated cAMP-PKA signaling has an important role in hepatic homeostasis and cytoprotection in vivo
Loss of the VIP gene orchestrates a panoply of pathogenic genes which are detrimental to both left and right cardiac homeostasis.
Vasoactive intestinal peptide may be an essential factor for Hertwig's epithelial root sheath development.
With cyclophosphamide-induced cystitis,VIP transcript expression significantly increased in the urothelium (48 h) of NGF-OE mice.
Peritoneal cells isolated from VIP KO naive mice produced lower levels of proinflammatory cytokines in response to LPS (show TLR4 Proteins) in vitro.
The protein encoded by this gene belongs to the glucagon family. It stimulates myocardial contractility, causes vasodilation, increases glycogenolysis, lowers arterial blood pressure and relaxes the smooth muscle of trachea, stomach and gall bladder. Alternative splicing occurs at this locus and two transcript variants encoding distinct isoforms have been identified.
, vasoactive intestinal peptide
, histidine-isoleucine/vasoactive intestinal polypeptide
, vasoactive intestinal polypeptide type I
, vasoactive intestinal polypeptide
, vasoactive instestinal peptide
, PHI, peptide histidine isoleucine