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Questions related from Martin Schnitzler
Hello, I use heat-inactivated sera for my cell culture experiments. The main goal of the heat-inactivation is to inactivate the complement system. I have now decided that it would be best to...
23 September 2020 3,203 1 View
Hello, I want to present my cytometry data using histograms/scatter dot plots. I thought I should focus on MFI to export my data. However, in some cases where I see a change in the percentage of...
20 December 2019 4,010 3 View
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Hello, I did some flow cytometry acquisition a week ago. Now, I finally got the chance to analyze the data and I unfortunately discovered that one of my compensation controls didn't work well:...
23 September 2019 6,239 4 View
Hello, I wanted to know if someone could explain to me why gating on negative populations of an unstained sample and a FMO control sample is sometimes different? (see screenshorts below) And...
09 September 2019 3,114 5 View
09 September 2019 9,680 4 View
Hello, I have been told that adjusting PMT voltages to lower compensation values is not a good practice. I found this PDF document (attached below) that is supposed to explain the impact of...
05 May 2019 3,741 1 View
Hello, I am using the LIVE/DEAD™ Fixable Aqua Dead Cell Stain from Thermofisher (https://www.thermofisher.com/order/catalog/product/L34965), to distinguish dead cells. I use it on freshly...
05 May 2019 336 2 View