Does anyone have any information on sorting micelles, liposomes, or liposome-like compartments? I would like to do in vitro transcription/translation in some sort of compartment (about 1.5 micron diameter) and directly measure properties using flow cytometry (NOT fuse these liposomes to cells, then sort). I found a protocol for doing this sort of transcription/translation in a water/mineral oil emulsion, but I'm pretty sure that I can't run mineral oil through the cytometer. Any ideas? Thanks- Brian Windsor Alan Lloyd Lab ICMB The University of Texas at Austin MBB 1.448B mail code: A4800 Austin, Texas 78713 (512) 471-3553 fax: (512) 232-3432 b.windsor@mail.utexas.edu
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