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Revision as of 16:28, 21 June 2016
Measurement with Flow Cytometry
This is a general guide for setting up your cells for flow cytometry readings in absolute units. These steps and questions are meant to provide a general protocol and we ask that you follow them to the best of your ability.
In order to carry out this measurement protocol, you will need:
- A flow cytometer with a channel configured for measurement of fluorescein (FITC) or GFP. This channel will typically have a 488nm laser an a 530/30 filter, but the details may vary.
- Fluorescent calibration beads that have been calibrated for Molecules of Equivalent FLuorescein (MEFL) or Molecules of Equivalent GFP (MEGFP). If available, we recommend using SpheroTech Rainbow Calibration Particles RCP-30-5A, as that is what the accompanying spreadsheet has been designed for.
All teams using a flow cytometer to measure GFP must finish the following items to fulfill the InterLab:
- Email your completed Excel file to measurement (AT) igem (DOT) org [note: the empty template file is provided below]
- Fill in the Flow Cytometer Form provided at the bottom of this page
- Create an InterLab study page on your team wiki (please use this format: https://2016.igem.org/Team:YourTeamName/InterLab)
Download the Excel Template file here: TeamName_iGEM2016_Flow_Cytometry_Worksheet.xls
You can see a filled-in example of the worksheet here
Important! If you have used a flow cytometer to measure GFP for the InterLab, please fill out the following Google Form to the best of your ability:
