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		<title>Molecular Biology Forum Life Science Forums - Flow Cytometry Forum</title>
		<link>http://www.molecularstation.com/forum/</link>
		<description>Flow Cytometry Forum. Discuss FACS cell sorting, flow cytometry, analysis and cell staining.</description>
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			<title>Molecular Biology Forum Life Science Forums - Flow Cytometry Forum</title>
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			<title>Autofluoresent macrophages</title>
			<link>http://www.molecularstation.com/forum/flow-cytometry-forum/71876-autofluoresent-macrophages.html</link>
			<pubDate>Thu, 19 Nov 2009 22:02:08 GMT</pubDate>
			<description>Are all murine macrophages autofluoresent? 
or do they differ depending on tissue?</description>
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<div>Are all murine macrophages autofluoresent?<br />
or do they differ depending on tissue?</div>


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			<category domain="http://www.molecularstation.com/forum/flow-cytometry-forum/">Flow Cytometry Forum</category>
			<dc:creator>hes</dc:creator>
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			<title>variable cell counts for staining</title>
			<link>http://www.molecularstation.com/forum/flow-cytometry-forum/71872-variable-cell-counts-staining.html</link>
			<pubDate>Thu, 19 Nov 2009 12:23:07 GMT</pubDate>
			<description>Dear all, 
 
I am using FACS to evaluate receptor expression on PMN. For each experiment, I got different groups (they only differ in the volatile...</description>
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<div>Dear all,<br />
<br />
I am using FACS to evaluate receptor expression on PMN. For each experiment, I got different groups (they only differ in the volatile anesthetic they are incubated with, the rest of the procedure is standardised and remains the same for all PMN). I therefore assume that there should not be any significant changes in cell count between groups. Regarding the AB-staining, would changes in PMN-counts (say +/- 30%) be a problem for further inter-group analysis? PMN are washed after staining...<br />
<br />
Thanks</div>


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			<category domain="http://www.molecularstation.com/forum/flow-cytometry-forum/">Flow Cytometry Forum</category>
			<dc:creator>brettsportler</dc:creator>
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			<title>Quantification?!</title>
			<link>http://www.molecularstation.com/forum/flow-cytometry-forum/71097-quantification.html</link>
			<pubDate>Wed, 04 Nov 2009 15:25:17 GMT</pubDate>
			<description>Dear all, 
 
how do you quantify or standardise your FACS results? I know there are several forms of quantification beads, e.g. Quantibrites from BD...</description>
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<div>Dear all,<br />
<br />
how do you quantify or standardise your FACS results? I know there are several forms of quantification beads, e.g. Quantibrites from BD for this purpose. But as I am using the same FACS-machine all the times and make sure that the voltage for the channel I´m looking at is constant, e.g. 600 for APC-Cy7, do I really need this???<br />
<br />
Thanks for your help, cheers<br />
<br />
Björn</div>


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			<category domain="http://www.molecularstation.com/forum/flow-cytometry-forum/">Flow Cytometry Forum</category>
			<dc:creator>brettsportler</dc:creator>
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			<title>flow cytometry help with scattergram</title>
			<link>http://www.molecularstation.com/forum/flow-cytometry-forum/70760-flow-cytometry-help-scattergram.html</link>
			<pubDate>Sun, 27 Sep 2009 22:31:40 GMT</pubDate>
			<description>Any help with a diagnosis would be appreciated.  Thanks.  
See attached scattergram picture.</description>
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<div>Any help with a diagnosis would be appreciated.  Thanks. <br />
See attached scattergram picture.</div>


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			<category domain="http://www.molecularstation.com/forum/flow-cytometry-forum/">Flow Cytometry Forum</category>
			<dc:creator>pathstudent</dc:creator>
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