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<title>Partial adherent cell fixation</title>
<link>http://www.scientistsolutions.com/t1183-partial+adherent+cell+fixation.html</link>
<description> Life Science Discussion</description>
<language>en-us</language> 
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<sy:updateBase>2005-05-05T12:00+00:00</sy:updateBase>
<item>
<title>Partial adherent cell fixation</title>
<link>http://www.scientistsolutions.com/t1183-partial+adherent+cell+fixation.html</link>
<description><![CDATA[We use 4% PFA for all our ICC and don't seem to have any problems.<br />We did try methanol/acetone 1:1 at one point &amp; that seemed to work fine as well (we were trying to troubleshoot a particular antibody that was giving us a headache).<br />I don't know if the addition of acetone would assist your situation, but might be worth a try if the PFA doesn't work.]]></description>
<pubDate>Mon, 10 Oct 2005 06:33:03 GMT</pubDate>
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<item>
<title>Partial adherent cell fixation</title>
<link>http://www.scientistsolutions.com/t1183-partial+adherent+cell+fixation.html</link>
<description><![CDATA[[quote=frasermoss]I always fixed with 4% paraformadahyde  (in PBS or TBS) without problems.  As long as you do the appropriate postitive and negative controls you should not have a problem either.[/quote]<br />Agreed.... 4% PFA has always worked for me too...  you might need to rinse off the PFA/PBS with whatever buffer base you are using for the stain IF there is some reaction or irregular staining with the PBS by the staining reagent.<br />The cells shrink due to the methanol being too 'drying'......]]></description>
<pubDate>Tue, 30 Aug 2005 03:38:10 GMT</pubDate>
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<item>
<title>Partial adherent cell fixation</title>
<link>http://www.scientistsolutions.com/t1183-partial+adherent+cell+fixation.html</link>
<description><![CDATA[I always fixed with 4% paraformadahyde  (in PBS or TBS) without problems.  As long as you do the appropriate postitive and negative controls you should not have a problem either.]]></description>
<pubDate>Wed, 10 Aug 2005 15:22:37 GMT</pubDate>
</item>
<item>
<title>Partial adherent cell fixation</title>
<link>http://www.scientistsolutions.com/t1183-partial+adherent+cell+fixation.html</link>
<description><![CDATA[Thanks to your suggestion first.<br />Fix with paraformaldehyde may be help, but if it compatible to staining solution? As I need to fix the cell and then stain the nucleus and cytoplasm. THX!]]></description>
<pubDate>Wed, 10 Aug 2005 01:43:31 GMT</pubDate>
</item>
<item>
<title>Partial adherent cell fixation</title>
<link>http://www.scientistsolutions.com/t1183-partial+adherent+cell+fixation.html</link>
<description><![CDATA[Why not use 0.02%-0.1% Triton X-100 instead (dissolved in your regular buffer e.g. PBS or TBS pH 7.4)? Incubate for about 15 min to get permableization.<br />Inclusion of small amounts of glutaraldehyde (0.1%) along with paraformaldehyde in the fixation step usually helps in preservation of cell structure and surface membrane proteins following permeabilisation by Triton X-100. In this case it may be necessary to determine if antigenicity is also maintained after glutaraldehyde is added.<br />If Tri...]]></description>
<pubDate>Tue, 09 Aug 2005 15:23:45 GMT</pubDate>
</item>
<item>
<title>Partial adherent cell fixation</title>
<link>http://www.scientistsolutions.com/t1183-partial+adherent+cell+fixation.html</link>
<description><![CDATA[Hi friends,<br />I am now doing with a cell line PU5-1.8, a marcophage like cell line. I want to fix it on cell culture treated coverslip and take to observe under microscope. But when I add mentanol to fix it, the cells turn to shrink and look ugly, just like a debris. Do anyone can give me some advice?<br />]]></description>
<pubDate>Tue, 09 Aug 2005 10:03:07 GMT</pubDate>
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