<p>In these experiments K69C expressing oocytes were first exposed to the test compound (50 µM, 5 minutes), then tested for responses to zinc, pH 6.5 and ATP, then exposed to the challenge compound (50 µM, 5 minutes). The purpose of the challenge compound application was to verify that the test compound had successfully bound to the K69C receptors. If it had not, then responses after the challenge compound would have been similar to the challenge compound given alone. Data for the MTSEA control are also shown in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0047147#pone-0047147-g001" target="_blank">Figure 1</a> and data for the AM546 control are also shown in <a href="http://www.plosone.org/article/info:doi/10.1371/...
Quantitative pharmacological studies were done to determine the properties of excitatory amino acid ...
Background/Purpose: Inward rectifying potassium channel 6.2 (Kir6.2 Δ C26 channel) is closely relate...
<p>HEK293 cells were co-transfected with expression constructs for either the <i>Am</i>DOP2 receptor...
<p>A–B: Sample traces from oocytes expressing either wild type rP2X2 (WT) or K69C as they were expos...
<p>A: Effect of suramin on an oocyte expressing wild type rP2X2 when applied without exogenous ATP. ...
<p>A: Responses of an oocyte before and after AM546 (50 µM, 15 minutes). The cell was then treated w...
<p>A: Responses to acidic pH and zinc before and after AM546 treatment. The dashed lines indicate th...
<p>(A,B) Representative Kir6.2/SUR1 currents recorded at -60mV from cell-attached patches on <i>Xeno...
<p>(A) Representative ramp tracings from an oocyte expressing ASIC1a before and after diminazene. Ra...
<p>(<i>A</i>) Current responses elicited by (10<i>E</i>,12<i>Z</i>)-hexadecadien-4-yn-1-ol (<b>10</b...
<p>Figure 2C Data. Current responses of oocytes expressing Cqui\Orco to 30µM OLC12 (~EC5) in the pre...
<p>The traces in (A) are examples of inward currents elicited by low agonist concentrations (in µM) ...
<p>(<b>A</b>) Representative current traces of oocytes expressing WT or mutant BmOr-1 or BmOrco. Bom...
<p>A) Oocytes injected with <i>Asu- unc-38</i> or <i>Asu-unc-29</i> cRNAs alone produced no function...
<p>The inhibition efficiency of each compound was examined at the concentration of 100 μM. The value...
Quantitative pharmacological studies were done to determine the properties of excitatory amino acid ...
Background/Purpose: Inward rectifying potassium channel 6.2 (Kir6.2 Δ C26 channel) is closely relate...
<p>HEK293 cells were co-transfected with expression constructs for either the <i>Am</i>DOP2 receptor...
<p>A–B: Sample traces from oocytes expressing either wild type rP2X2 (WT) or K69C as they were expos...
<p>A: Effect of suramin on an oocyte expressing wild type rP2X2 when applied without exogenous ATP. ...
<p>A: Responses of an oocyte before and after AM546 (50 µM, 15 minutes). The cell was then treated w...
<p>A: Responses to acidic pH and zinc before and after AM546 treatment. The dashed lines indicate th...
<p>(A,B) Representative Kir6.2/SUR1 currents recorded at -60mV from cell-attached patches on <i>Xeno...
<p>(A) Representative ramp tracings from an oocyte expressing ASIC1a before and after diminazene. Ra...
<p>(<i>A</i>) Current responses elicited by (10<i>E</i>,12<i>Z</i>)-hexadecadien-4-yn-1-ol (<b>10</b...
<p>Figure 2C Data. Current responses of oocytes expressing Cqui\Orco to 30µM OLC12 (~EC5) in the pre...
<p>The traces in (A) are examples of inward currents elicited by low agonist concentrations (in µM) ...
<p>(<b>A</b>) Representative current traces of oocytes expressing WT or mutant BmOr-1 or BmOrco. Bom...
<p>A) Oocytes injected with <i>Asu- unc-38</i> or <i>Asu-unc-29</i> cRNAs alone produced no function...
<p>The inhibition efficiency of each compound was examined at the concentration of 100 μM. The value...
Quantitative pharmacological studies were done to determine the properties of excitatory amino acid ...
Background/Purpose: Inward rectifying potassium channel 6.2 (Kir6.2 Δ C26 channel) is closely relate...
<p>HEK293 cells were co-transfected with expression constructs for either the <i>Am</i>DOP2 receptor...