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<title>calculated vs measured LJP</title>
<link>http://www.scientistsolutions.com/t22964-calculated+vs+measured+ljp.html</link>
<description> Life Science Discussion</description>
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<item>
<title>calculated vs measured LJP</title>
<link>http://www.scientistsolutions.com/t22964-calculated+vs+measured+ljp.html</link>
<description><![CDATA[ Ok, I have stopped using the agar bridge and instead started using a flowing KCl bridge. With this approach it worked fine. <br />I still don't understand why my agar bridges did not seem to work correctly.]]></description>
<pubDate>Thu, 16 May 2013 09:50:25 GMT</pubDate>
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<item>
<title>calculated vs measured LJP</title>
<link>http://www.scientistsolutions.com/t22964-calculated+vs+measured+ljp.html</link>
<description><![CDATA[Hi guys, I would like to ask a similar question.<br />I used JPCalc to calculate the liquid potential for my experiments, in order to verify the result I measured the liquid junction potential as well.<br />The problem that occurs is that when I change my aCSF bath solution for my internal solution the potential I measured before does not reverse, which it should.<br />Can somebody  give me some advice on this?<br />My measurement procedure is as follows:<br />I start with internal solution i...]]></description>
<pubDate>Tue, 14 May 2013 05:29:23 GMT</pubDate>
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<item>
<title>calculated vs measured LJP</title>
<link>http://www.scientistsolutions.com/t22964-calculated+vs+measured+ljp.html</link>
<description><![CDATA[ I am just curious to know how you calculated the LJP.<br />Would you provide the composition of both intra and bath solutions? I understand Igor is the software, not program.<br />How you measured the LJP? By changing the bath solution to the another one? Do you have the agar bridge between recording chamber and the reference electrode? <br />Thanks.]]></description>
<pubDate>Thu, 26 Apr 2012 16:05:06 GMT</pubDate>
</item>
<item>
<title>calculated vs measured LJP</title>
<link>http://www.scientistsolutions.com/t22964-calculated+vs+measured+ljp.html</link>
<description><![CDATA[I am using two different intracellular pipette solutions and one bath solution (standard ACSF) to measure NMDAR-IV curves in CA1 pyramidal cells. I am trying to correct for the liquid junction potential of my two different internals, but the values I calculated using Igor (10mV and 8.4mV) are very different from what I've measured on my rig (26mV and 22mV). <br />Please advise on which numbers I should use to correct my membrane voltage, and what could be causing such a large discrepancy ...]]></description>
<pubDate>Thu, 26 Apr 2012 13:56:53 GMT</pubDate>
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