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M00205
CHO-K1/V1B Stable Cell Line
2 vials
Product Name CHO-K1/V1B Stable Cell Line
Full Name
Human Recombinant V1B Vasopressin Receptor Stable Cell Line
Documents
Document-EXAMPLE: 9777_20090520040910.JPG (JPG)
TECHNICAL MANUAL: 9836_20090524233630.PDF (PDF)
Document-MSDS: 10392_20090813065548.PDF (PDF)
Figures
Reference
Species
Human
Description
The antidiuretic hormone arginine vasopressin (AVP) receptors are G protein-coupled receptors which consists of at least three types: V1A (vascular/hepatic) and V1B (anterior pituitary) receptors, which act through phosphatidylinositol hydrolysis to mobilize intracellular Ca2+; and V2 (kidney) receptor, which is coupled to adenylate cyclase. V1B receptors are expressed in anterior pituitary where they mediate the release of ACTH . Its peripheral actions, such as antidiuresis, contraction of vascular smooth muscle, and stimulation of hepatic glycogenolysis are well characterized.
Freeze Medium
45% culture medium, 45% FBS, and 10% DMSO
Culture Medium
Ham's F12, 10% FBS, 400 μg/ml G418
Storage
Liquid nitrogen immediately upon delivery
Application
Functional assay for V1B receptor
Application Examples
Figure 1. AVP-induced concentration-dependent stimulation of intracellular calcium mobilization in CHO-K1/V1B and CHO-K1 cells. The cells were loaded with Calcium-4 prior to stimulation with a V1B receptor agonist, AVP. The intracellular calcium change was measured by FlexStation. The relative fluorescent units (RFU) were plotted against the log of the cumulative doses (10-fold dilution) of AVP (Mean ± SD, n = 2). The EC50 of AVP on V1B in CHO-K1 cells was 0.12 nM. The S/B of AVP on V1B in CHO-K1 cells was 46.
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