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<p class=MsoNormal>Hi, <o:p></o:p></p>
<p class=MsoNormal>What are the optical sedimentation observation boundaries
for the fluorescence detector? I do not have access to the system currently. A
friend sent me his data. I have the impression that in this particular run the
entire signal is shifted toward smaller radii. My impression was always, that
the cell gets illuminated to about 7.1 cm before the bottom gets visible due to
the dye quenching. My suspicion is that the radial calibration is off on this
machine. <o:p></o:p></p>
<p class=MsoNormal>Thanks for your help<o:p></o:p></p>
<p class=MsoNormal>Best, <o:p></o:p></p>
<p class=MsoNormal>Titus<o:p></o:p></p>
<p class=MsoNormal><o:p> </o:p></p>
<p class=MsoNormal>Titus M. Franzmann<o:p></o:p></p>
<p class=MsoNormal><o:p> </o:p></p>
<p class=MsoNormal><o:p> </o:p></p>
<p class=MsoNormal>University of Michigan<o:p></o:p></p>
<p class=MsoNormal>Molecular, Cellular, <o:p></o:p></p>
<p class=MsoNormal> Developmental and Biology (MCDB)<o:p></o:p></p>
<p class=MsoNormal><span lang=DE>4140 Nat. Sci. Bldg<o:p></o:p></span></p>
<p class=MsoNormal><span lang=DE>830 North University<o:p></o:p></span></p>
<p class=MsoNormal><span lang=DE>Ann Arbor, Mi, 48109<o:p></o:p></span></p>
<p class=MsoNormal><span lang=DE>USA<o:p></o:p></span></p>
<p class=MsoNormal><span lang=DE><o:p> </o:p></span></p>
<p class=MsoNormal><span lang=DE>Tel: +1 (734) 647 2291<o:p></o:p></span></p>
<p class=MsoNormal><span lang=DE>eMail: <a href="mailto:tmfr@umich.edu"
title="send an email to tmfr@umich.edu">tmfr@umich.edu</a><o:p></o:p></span></p>
<p class=MsoNormal><span lang=DE>web: <a
href="http://www.mcdb.lsa.umich.edu/labs/walter/"
title="click to visit the walter lab web sites">walter lab website</a><o:p></o:p></span></p>
<p class=MsoNormal><o:p> </o:p></p>
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