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Analysis

Sample Preparation

We strongly reccommend that you filter your cells prior to running on any of our instruments, there are various filter options available, please discuss with a member of the core facility.  This is a great article on ways to prevent clumping:

Flow Cytometry Protocols To Prevent Sample Clumping

Running correct controls are very important, you should come with at least the following:

  • Biological Controls
  • FMO Controls for multi-color experiments to set Negative gates
  • Compensation Controls
  • QC Controls such as beads to take into account instrument changes over time.
  • Proper Panel Design will also ensure you produce excellent data!

The flow core strongly recommends that you use a Live/Dead marker in all of your panels.

How many events should i collect?

Meet the Team


David Archer, PhD

Scientific Director, Pediatric+Winship Flow Cytometry Core and Animal Physiology Core

darcher@emory.edu

Aaron Rae

Core Technical Director, Pediatric+Winship Flow Cytometry Core

ajrae@emory.edu

Igor Albizua-Santin

Flow Cytometry Technologist Supervisor

ialbizu@emory.edu

Ashley Jones, MS

Flow Cytometry Technologist, Sr

ashley.jones@emory.edu

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