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Cat. No.
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M00431
CHO-K1/NPFF1/Gα15 Stable Cell Line
2 vials
Product Name CHO-K1/NPFF1/Gα15 Stable Cell Line
Full Name
Human Recombinant Neuropeptide FF Receptor 1 Stable Cell Line
Documents
Document-EXAMPLE: 12926_20100611025015.JPG (JPG)
TECHNICAL MANUAL: 13098_20100712065828.PDF (PDF)
Document-MSDS: 13229_20100815212507.PDF (PDF)
Figures
Reference
Species
Human
Description
The neuropeptide FF receptors are members of the G-protein coupled receptor superfamily of integral membrane proteins which bind the pain modulatory neuropeptides AF and FF. These neuropeptides are thought to be involved in modulation of opioid receptor function in the brain and spinal cord, and can either reduce or increase opioid receptor function depend which tissue they are released in, reflecting a complex role for neuropeptide FF in pain responses.
Freeze Medium
45% culture medium, 45% FBS, 10% DMSO
Culture Medium
Ham's F12, 10% FBS, 200 μg/ml Zeocin, 100 μg/ml Hygromycin B
Storage
Liquid nitrogen immediately upon delivery
Application
Functional assay for NPFF1 receptor
Application Examples
Figure 1. RFRP-3-induced concentration-dependent stimulation of intracellular calcium mobilization in CHO-K1/NPFF1/Gα15 and CHO-K1/Gα15 cells. The cells were loaded with Calcium-4 prior to stimulation with an NPFF1 receptor agonist, RFRP-3. The intracellular calcium change was measured by FlexStation. The relative fluorescent units (RFU) were plotted against the log of the cumulative doses (5-fold dilution) of RFRP-3 (Mean ± SD, n = 2). The EC50 of RFRP-3 on NPFF1 co-expressing with Gα15 in CHO-K1 cells was 22 nM. The S/B of RFRP-3 on NPFF1 co-expressing with Gα15 in CHO-K1 cells was 6.
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