Hello,

I am planning to conduct an experiment to identify bacteria bound to IgG by flow cytometry. I aim to focus on live bacteria, so I intend to use the LIVE/DEAD BacLight Kit (Syto9 and propidium iodide) to confirm I'm examining live bacteria. Since I need to fix the samples before acquisition on the flow cytometer, my questions are:

  • Is it possible to fix samples when using the LIVE/DEAD BacLight Kit?
  • Should I perform IgG staining before or after the LIVE/DEAD staining?
  • Thanks in advance,

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