glosensor camp kit (Promega)
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Glosensor Camp Kit, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/glosensor+camp+assay/glosensor+camp+assay/pm40670604-246-1-5
Average 90 stars, based on 1 article reviews
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cAMP Assay:Article Title: Antagonists Enhance Cell-Surface Expression of Mammalian Odorant Receptors Article Snippet: All odorants were purchased from FUJIFILM Wako Chemicals (Osaka, Japan) and TCI Chemicals (Tokyo, Japan). .. A Article Title: Compositions and methods for anti-PACAP antibodies Article Snippet: .. In addition, the antibody-independent Article Title: Regulation of CXCR4 function by S1P 1 through heteromerization. Article Snippet: Flow cytometry data were processed with FlowJo software, and relative cell surface expression of GPCRs was expressed as mean fluorescence intensity (MFI). .. Quantification of cAMP production was conducted using the Article Title: Relaxin-2 fusion proteins Article Snippet: Cell Culture and Maintenance HEK293 cells (ATCC CRL-1573) were cultured in DMEM+10% FBS, 1% (1× or 10 U/mL) Pen-Strep in a humidified CO2 incubator at 37 C, 5% CO2 until 80-100% confluency. .. Cells were typically split 1:6 for 3 days and maintained in a sterile T-75 tissue culture flask. cAMP Signaling Assay Protocol This protocol was adapted from the Article Title: Docking 14 Million Virtual Isoquinuclidines against the μ and κ Opioid Receptors Reveals Dual Antagonists–Inverse Agonists with Reduced Withdrawal Effects Article Snippet: .. To assess Gi/omediated cAMP production inhibition we followed a protocol modified from the Article Title: Antagonists Enhance Cell-Surface Expression of Mammalian Odorant Receptors Article Snippet: All odorants were purchased from FUJIFILM Wako Chemicals (Osaka, Japan) and TCI Chemicals (Tokyo, Japan). .. A Article Title: Docking 14 Million Virtual Isoquinuclidines against the μ and κ Opioid Receptors Reveals Dual Antagonists–Inverse Agonists with Reduced Withdrawal Effects Article Snippet: .. To assess G i/o -mediated cAMP production inhibition we followed a protocol modified from the Promega Activation Assay:Article Title: Antagonists Enhance Cell-Surface Expression of Mammalian Odorant Receptors Article Snippet: All odorants were purchased from FUJIFILM Wako Chemicals (Osaka, Japan) and TCI Chemicals (Tokyo, Japan). .. A Article Title: Antagonists Enhance Cell-Surface Expression of Mammalian Odorant Receptors Article Snippet: All odorants were purchased from FUJIFILM Wako Chemicals (Osaka, Japan) and TCI Chemicals (Tokyo, Japan). .. A Ligand Binding Assay:Article Title: Antagonists Enhance Cell-Surface Expression of Mammalian Odorant Receptors Article Snippet: All odorants were purchased from FUJIFILM Wako Chemicals (Osaka, Japan) and TCI Chemicals (Tokyo, Japan). .. A Article Title: Antagonists Enhance Cell-Surface Expression of Mammalian Odorant Receptors Article Snippet: All odorants were purchased from FUJIFILM Wako Chemicals (Osaka, Japan) and TCI Chemicals (Tokyo, Japan). .. A Luciferase:Article Title: Compositions and methods for anti-PACAP antibodies Article Snippet: .. In addition, the antibody-independent other:Article Title: Structural basis of stepwise proton sensing-mediated GPCR activation Article Snippet: The accumulation of cAMP upon proton activation was quantified using the Sterility:Article Title: Relaxin-2 fusion proteins Article Snippet: Cell Culture and Maintenance HEK293 cells (ATCC CRL-1573) were cultured in DMEM+10% FBS, 1% (1× or 10 U/mL) Pen-Strep in a humidified CO2 incubator at 37 C, 5% CO2 until 80-100% confluency. .. Cells were typically split 1:6 for 3 days and maintained in a sterile T-75 tissue culture flask. cAMP Signaling Assay Protocol This protocol was adapted from the Inhibition:Article Title: Docking 14 Million Virtual Isoquinuclidines against the μ and κ Opioid Receptors Reveals Dual Antagonists–Inverse Agonists with Reduced Withdrawal Effects Article Snippet: .. To assess Gi/omediated cAMP production inhibition we followed a protocol modified from the Article Title: Docking 14 Million Virtual Isoquinuclidines against the μ and κ Opioid Receptors Reveals Dual Antagonists–Inverse Agonists with Reduced Withdrawal Effects Article Snippet: .. To assess G i/o -mediated cAMP production inhibition we followed a protocol modified from the Promega Modification:Article Title: Docking 14 Million Virtual Isoquinuclidines against the μ and κ Opioid Receptors Reveals Dual Antagonists–Inverse Agonists with Reduced Withdrawal Effects Article Snippet: .. To assess Gi/omediated cAMP production inhibition we followed a protocol modified from the Article Title: Docking 14 Million Virtual Isoquinuclidines against the μ and κ Opioid Receptors Reveals Dual Antagonists–Inverse Agonists with Reduced Withdrawal Effects Article Snippet: .. To assess G i/o -mediated cAMP production inhibition we followed a protocol modified from the Promega Cell Culture:Article Title: Docking 14 Million Virtual Isoquinuclidines against the μ and κ Opioid Receptors Reveals Dual Antagonists–Inverse Agonists with Reduced Withdrawal Effects Article Snippet: .. To assess Gi/omediated cAMP production inhibition we followed a protocol modified from the Transfection:Article Title: Docking 14 Million Virtual Isoquinuclidines against the μ and κ Opioid Receptors Reveals Dual Antagonists–Inverse Agonists with Reduced Withdrawal Effects Article Snippet: .. To assess Gi/omediated cAMP production inhibition we followed a protocol modified from the |
![( A ) An inhibition of 5-HT 1A R–mediated cAMP accumulation is observed for serotonin, befiradol, and ST171. The stimulation of cAMP accumulation in the presence of PTX suggests an additional G s response for befiradol and serotonin (serotonin: EC 50 = 52 ± 6 nM; befiradol: EC 50 = 25 ± 11 nM) but not for ST171. Data were obtained in three to five independent experiments with a CAMYEL assay in CHO-K1 cells. ( B ) Inhibition of cAMP accumulation by serotonin, befiradol, and ST171 in HEK293A cells deficient of G s proteins and ( C ) accumulation of cAMP by serotonin and befiradol but not ST171 in HEK293A cells deficient of G i/o proteins. Data were obtained with a <t>GloSensor</t> in n = 6 experiments, each performed in triplicates. ( D ) ST171 inhibits cAMP accumulation caused by 1 μM serotonin in HEK293AΔG i/o cells and thus demonstrates functional antagonism for the activation of G s proteins (IC 50 = 3.9 ± 0.8 nM). Data were obtained with the GloSensor in n = 3 independent experiments, each performed as triplicates. ( E ) β-Arrestin 1 and ( F ) β-arrestin 2 recruitment is monitored by bystander BRET in HEK293T cells with elevated GRK2 levels [ n = 4 to 6 (β-arrestin 1) or 11 to 14 (β-arrestin 2) independent experiments]. ( G ) ST171 is a functional antagonist (IC 50 = 3.9 ± 0.5 nM) for 5-HT 1A R–mediated β-arrestin 2 recruitment stimulated with serotonin (1 μM, ~EC 80 ). Data were obtained with the PathHunter assay in the absence of GRK2 in three independent experiments, each performed in triplicates. All data were normalized to the maximum response of serotonin and are indicated as the means ± SEM of n independent experiments.](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_5894/pmc12175894/pmc12175894__sciadv.adv9267-f2.jpg)