ra1ar membranes (Revvity)
Structured Review
![Figure 1. (A) Functional activity of agonists 2 and 7, in stimulation of guanine nucleotide binding at the <t>rA1AR</t> (recombinant A1AR membrane preparations from CHO-K1 cells, PerkinElmer, compared to 2). (B) Effects of agonists 7 and 16 in inhibition of cAMP accumulation at hA3AR (in A3AR-expressing CHO cells, treated with 10 μM forskolin, compared to 16). 100% value is defined as effect of 1 μM 16. Also, functional assays at the hA1AR are shown for several derivatives (EC50 or IC50 in nM): stimulation of [35S]GTPγS binding (C, 9, 28.0 ± 9.0; 16, 0.12 ± 0.05; 40, 758 ± 175); inhibition of forskolin-stimulated cAMP production (D, 9, 0.14; 40, 87); β-arrestin2 recruitment (E, 9, 209 ± 90; 16, 5.03 ± 2.84; 40, 2460 ± 800).](https://doi-unpaywalled-images-cdn.bioz.com/6428/10__1021_slash_acs__jmedchem__8b01662/10__1021_slash_acs__jmedchem__8b01662____page9_image1.jpg)
Ra1ar Membranes, supplied by Revvity, used in various techniques. Bioz Stars score: 90/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ra1ar+membranes/10__1021_slash_acs__jmedchem__8b01662-483-14-16?v=Revvity
Average 90 stars, based on 2 article reviews
Images
1) Product Images from "Design and in Vivo Characterization of A1 Adenosine Receptor Agonists in the Native Ribose and Conformationally Constrained (N)-Methanocarba Series"
Article Title: Design and in Vivo Characterization of A1 Adenosine Receptor Agonists in the Native Ribose and Conformationally Constrained (N)-Methanocarba Series
Journal: Journal of Medicinal Chemistry
doi: 10.1021/acs.jmedchem.8b01662
Figure Legend Snippet: Figure 1. (A) Functional activity of agonists 2 and 7, in stimulation of guanine nucleotide binding at the rA1AR (recombinant A1AR membrane preparations from CHO-K1 cells, PerkinElmer, compared to 2). (B) Effects of agonists 7 and 16 in inhibition of cAMP accumulation at hA3AR (in A3AR-expressing CHO cells, treated with 10 μM forskolin, compared to 16). 100% value is defined as effect of 1 μM 16. Also, functional assays at the hA1AR are shown for several derivatives (EC50 or IC50 in nM): stimulation of [35S]GTPγS binding (C, 9, 28.0 ± 9.0; 16, 0.12 ± 0.05; 40, 758 ± 175); inhibition of forskolin-stimulated cAMP production (D, 9, 0.14; 40, 87); β-arrestin2 recruitment (E, 9, 209 ± 90; 16, 5.03 ± 2.84; 40, 2460 ± 800).
Techniques Used: Functional Assay, Activity Assay, Binding Assay, Recombinant, Membrane, Inhibition, Expressing