Why not stop the reactions by fixing the cells? Its as easy as keeping on ice. John -----Original Message----- From: Julie Nelson [mailto:jnelson@uga.edu] Sent: Wednesday, December 15, 2004 5:10 PM To: cyto-inbox Subject: Holding phagocytosis assays Hi ya'll, One of my users poses the following question: "In a phagocytosis assay, is there any point in the procedure at which the reaction could be "put on ice" (literally or metaphorically)? I ask this question for a couple of reasons: the animals will be housed at the Savannah River Ecology Lab (2.5 hours drive from Athens), and I will be working with a large number of animals, and even with help, I may not be able to euthanize all the animals on the same day. I haven't found anything in the literature that suggests that it would be okay to have any kind of delays. The protocols include brief incubations, but there seems to be no clear "holding point" in any of the assays." I imagine she'll be using either beads or FITC-labelled bacteria. Can you help? Happy holidays and thanks in advance, Julie Julie Nelson Research Coordinator Flow Cytometry Facility Center for Tropical and Emerging Global Diseases University of GeorgiaReceived on Thu Dec 16 12:38:00 2004
This archive was generated by hypermail 2.1.8 : Fri Dec 17 2004 - 03:12:05 EST