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	<id>https://bridgeslab.sph.umich.edu/protocols/index.php?action=history&amp;feed=atom&amp;title=Rab5_FRET_Assay</id>
	<title>Rab5 FRET Assay - Revision history</title>
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	<updated>2026-06-02T00:36:39Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<id>https://bridgeslab.sph.umich.edu/protocols/index.php?title=Rab5_FRET_Assay&amp;diff=519&amp;oldid=prev</id>
		<title>Davebrid: wrote initial protocol</title>
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		<updated>2010-09-16T14:18:46Z</updated>

		<summary type="html">&lt;p&gt;wrote initial protocol&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;[[Category:FRET]]&lt;br /&gt;
[[Category:Swanson]]&lt;br /&gt;
[[Category:CLCI]]&lt;br /&gt;
&lt;br /&gt;
==Materials==&lt;br /&gt;
*mCitrine-Rab5BD (from EEA1/NT)&lt;br /&gt;
*mCFP-Rab5A&lt;br /&gt;
*Acid etched Coverslips (see [[Acid Etching Coverslips]])&lt;br /&gt;
*Cells of interest&lt;br /&gt;
&lt;br /&gt;
==Protocol==&lt;br /&gt;
*Plate out ~150 000 cells per well in a 6 well dish with an acid etched coverslip&lt;br /&gt;
*The next morning transfect cells with [[Fugene Transfection of 293T/COS Cells|Fugene]], [[Lipofectamine Plasmid Transfection|Lipofectamine]] or other protocol&lt;br /&gt;
*That evening replace with fresh media (and serum starve if doing insulin/growth factor stimulation&lt;/div&gt;</summary>
		<author><name>Davebrid</name></author>
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