Does anyone have any experience sorting bacteria from stool samples? Specifically, what dyes were used to identify the bacteria, how much debris impacted the sorting, and whether or not you could distinguish between bacteria aggregates and single bacteria? Currently, we are attempting to use a DNA stain like DAPI or PI on fixed samples, but are running into problems with aggregated bacteria due to the presence of biofilms in the sample. I'm sure the fixation process is not helping, but from a biohazard standpoint, we'd prefer to fix. The ability to accurately sort a single bacteria is of most concern. We'd prefer the ability to get rid of any aggregates at the cost of yield. We have a MoFlo with a 488, 633, and an unreliable I90-K and a FACSAria with a 405nm, 488nm and 633nm. Any help would be greatly appreciated thanks, Ryan ----------------------------------------------- Ryan Duggan Technical Director Flow Cytometry Facility University of Chicago Ph: 773.702.9212 or .5582 Web: http://ucflow.uchicago.edu Main Facility 910 E. 58th, Room 037 Chicago, IL 60637 ----------------------------------------------- This email is intended only for the use of the individual or entity to which it is addressed and may contain information that is privileged and confidential. If the reader of this email message is not the intended recipient, you are hereby notified that any dissemination, distribution, or copying of this communication is prohibited. If you have received this email in error, please notify the sender and destroy/delete all copies of the transmittal. Thank you.Received on Tue Feb 12 13:18:00 2008
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