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Human VIPR2/beta-Arrestin Stable Cell Line-CHO

Cat.No.
CSC-RG1613
Abbr
CHO-HuVIPR2/beta-Arrestin
Alias
VIPR2,VPAC2,VPAC2R,VIP-R-2,VPCAP2R,PACAP-R3,DUP7q36.3,PACAP-R-3,C16DUPq36.3,FLJ16511
Growth Properties
Adherent
Host Cell
CHO-K1
Morphology
Epithelial-like
Shipping
Dry ice
Species
Human
Background
Vasoactive intestinal peptide (VIP), a 28 amino acid peptide originally isolated by its vasodilation activity, binds to two class B GPCRs, VPAC1 and VPAC2, to exert its functions in the CNS, vasculature, immune system and adrenal medulla. In the immune system, VPAC2 is expressed on stimulated CD4 T cells, and binding of T cell-derived VIP to VPAC2 induces a shift toward the Th2 pathway. In addition, VPAC2 is an essential regulator of the circadian pacemaker of the hypothalamic suprachiasmatic nuclei.

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