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CRB1001039 - VIP (guinea pig)

CRB1001039

VIP (guinea pig)

Vasoactive intestinal peptide (VIP) is a neuropeptide found throughout the body and the central nervous system. VIP is located within cell bodies and nerve endings of the enteric nervous system, brain and pancreas. VIP neurons in the peripheral ... Read More
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  Strictly for Research Purposes only. Not for Personal or Veterinary use.

Update on Shipping Rates — Effective May, 2026
Synonyms
H-HSDALFTDTYTRLRKQMAMKKYLNSVLN-NH2
gp VIP
HSDALFTDTYTRLRKQMAMKKYLNSVLN-amide
H-His-Ser-Asp-Ala-Leu-Phe-Thr-Asp-Thr-Tyr-Thr-Arg-Leu-A rg-Lys-Gln-Met-Ala-Met-Lys-Lys-Tyr-Leu-Asn -Ser-Val-Leu-Asn-NH2
Beta amyloid
gp VIP
Product Code
CRB1001039
Molecular Weight
3,342.7 g/mol
Long Term Storage
store at <-15°C
Storage
store at <-15°C
Harmonized Tariff Codes
Switzerland: 29337900 - USA: 2933798500 - Slovakia: 2933790090 - UK: 2933790090 - China: 2933790099
Vasoactive intestinal peptide (VIP) is a neuropeptide found throughout the body and the central nervous system. VIP is located within cell bodies and nerve endings of the enteric nervous system, brain and pancreas. VIP neurons in the peripheral system fire to regulate blood vessels, and the? CNS innervate cerebral vasculature. VIP ?binds to G protein-coupled receptors VPAC1 and VPAC2. VIP and VPAC2 are detected in circular smooth muscle cells of cerebral arterioles. VIP and VPAC1 are also found in lymphatic tissue. VIP can block inflammation, modify the Th response favouring Th2 and induce regulatory T cells. Overexpression of each receptor has been linked to various cancers.
VIP administration leads to pancreatic bicarbonate-rich fluid secretion but not to the same degree stimulated by secretin. VIP stimulates insulin secretion in a glucose-dependent manner and also stimulates glucagon secretion. Studies have found that in morbidly obese patients, VIP levels are lowered and work to slow gastric and duodenal motility but increase gastric emptying. Therefore, decreasing VIP levels in obese patients may increase weight gain by accelerating gastric emptying.
VIP has been well studied in pancreatic acini. VIP is a full agonist of amylase secretion and increases cyclic AMP synchronised with an increase in intracellular Ca2+ triggered by stimuli that act through cholecystokinin (CCK) or cholinergic agonists. Most cAMP increases and amylase secretion appears to be mediated via VPAC1.
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MSDS
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TSE / BSE Statement
TSE-BSE declaration VIP (guinea pig) CRB1001039
Retest Statement
Retest Statement VIP (guinea pig) CRB1001039
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