Endy:FACS protocols: Difference between revisions
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==Media== | ==Media== | ||
As | As described in the standard protocol we often use [[M9_medium/supplemented|Supplemented M9 media]] although we are now switching to using [[Neidhardt_EZ_Rich_Defined|EZ media]] where possible. | ||
==Bead calibration== | ==Bead calibration== | ||
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==Data analysis== | ==Data analysis== | ||
We do all our analysis using [http://www.flowjo.com/ | We do all our analysis using [http://www.flowjo.com/ FlowJo] and [http://mathworks.com Matlab]. | ||
''Information aggregated by [[Barry Canton]].'' | |||
[[Category:Protocol]] [[Category:Flow cytometry]] |
Latest revision as of 07:51, 5 September 2007
Protocol
Here is a basic standard protocol that we try and use in the Endy and Knight labs. Exact conditions may depend on the strain, induction conditions etc.
Equipment
When we are doing flow experiments, we normally use a FACScan cytometer, described here. Some lab members have experience using the MoFlo machines also. We also have an NPE flow cytometer that we use in our lab for some experiments.
Media
As described in the standard protocol we often use Supplemented M9 media although we are now switching to using EZ media where possible.
Bead calibration
We calibrate results from day to day using this bead protocol.
Data analysis
We do all our analysis using FlowJo and Matlab.
Information aggregated by Barry Canton.