Flow Basics 2.5: Instrument Setup and Automated Compensation

  Рет қаралды 9,986

UChicago Flow

UChicago Flow

Күн бұрын

Flow Basics 2.0 is a series of courses that builds on the original Flow Basics course. This series outlines all of the practical steps for setting up a flow cytometry experiment and highlights factors that impact final results.
This course covers:
-Organizing the experimental layout (1:37)
-Setting Voltages (13:05)
-Automated Compensation (29:34)
-How to identify compensation errors
Download the slides: voices.uchicago.edu/ucflow/pr...

Пікірлер: 4
@florianmarquet4324
@florianmarquet4324 Жыл бұрын
series of high quality presentations, I have been doing cytometry for 15 years, this will allow me to explain with precision what I was doing without sometimes knowing why
@annalau9645
@annalau9645 2 жыл бұрын
Bravo!!!!
@THE_LN_PLAYS
@THE_LN_PLAYS 3 жыл бұрын
Thank you for an excellent course. I am new to flow cytometry - how do you ensure that a single stained control / compensation control is brighter than overall sample, if the cell population we are targeting (in a compensation control tube) has low expression of surface marker? I would assume that a fluorophore-conjugated low expression surface marker would not emit high fluorescence signal due to small number of cells expressing said marker, even if the cell suspension is stained with a bright dye such as PE. Thank you for your help.
@UChicagoFlow
@UChicagoFlow 3 жыл бұрын
Hi! This can be a tricky question. First I want to point out that the frequency and intensity of a marker are distinct features and independent from each other. You can have a low frequency population (
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