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M00155
293/FP/Gα15 Stable Cell Line
2 vials
Product Name 293/FP/Gα15 Stable Cell Line
Full Name
Human Recombinant FP Prostanoid Receptor Stable Cell Line
Documents
Document-EXAMPLE: 9778_20090520044926.JPG (JPG)
TECHNICAL MANUAL: 9835_20090524225814.PDF (PDF)
Document-MSDS: 10375_20090813060746.PDF (PDF)
Figures
Reference
Species
Human
Description
Prostaglandin F (2-alpha) is known as a potent luteolytic agent. It is involved in modulating intraocular pressure and smooth muscle contraction in uterus. Its effects on cells are mediated through specific interaction with the Prostanoid receptor FP, which is a 359-amino acid protein. Having 7 putative transmembrane domains, FP resembles the characteristic of G protein coupled receptors. Knockout studies in mice suggest that the interaction of PGF2-alpha with this receptor may initiate parturition in ovarian luteal cells and thereupon induce luteolysis.
Freeze Medium
45% culture medium, 45% FBS, 10% DMSO
Culture Medium
DMEM, 10% FBS, 200 μg/ml Zeocin, 250 μg/ml G418, 100 μg/ml Hygromycin B
Storage
Liquid nitrogen immediately upon delivery
Application
Functional assay for FP receptor
Application Examples
Figure 1. Cloprostenol-induced concentration-dependent stimulation of intracellular calcium mobilization in 293/FP/Gα15 and 293 cells. The cells were loaded with Calcium-4 prior to stimulation with an FP receptor agonist, Cloprostenol. 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 Cloprostenol (Mean ± SD, n = 2). The EC50 of Cloprostenol on FP co-expressing with Gα15 in 293 cells was 25 nM. The S/B of Cloprostenol on FP co-expressing with Gα15 in 293 cells was 31.
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