Author Archive
Future Proofing Your Experiments and Files: The Importance of Annotation
Ever find yourself staring at a folder of FCS files and thinking, “Wait, now which tubes did I add PMA to, how much did I add, and which samples were these again?”
Jonathan from Cytobank/Stanford recommends what he calls “future proofing” in order to avoid this problem. He explained this approach during a CYTO 2011 Pre-Congress course in his talk titled “Flood Cytometry: Embracing Single Cell Systems Biology (and coping with large cytometry experiments).” In that talk, he outlined four easy steps that are useful for experiments of all sizes.
When collecting on the cytometer:
- Tag your FCS files with key experiment details (e.g. “Patient-J01 IL-2 15m”)
- Label the channels you are measuring (before collecting data)
- Make sure scales and compensations work (before collecting data)
- Encode clinical sample IDs (don’t use HIPAA sensitive information)
Upcoming Meetings: July – September 2011
Our summer travels are not quite over! Come say hello and tell us how you’re using Cytobank to share and analyze your flow data.
Upcoming Meetings: June 2011
We’re coming to a city near you. Come say hello and tell us how you’re using Cytobank to share and analyze your flow data.
Upcoming Meetings: IMMUNOLOGY 2011 and CYTO 2011
We’re excited to be attending both IMMUNOLOGY 2011 and CYTO 2011 in the next couple weeks. Come say hello and tell us how you’re using Cytobank to share and analyze your flow data.
May 13-17, 2011
IMMUNOLOGY 2011
98th Annual Meeting of the American Association of Immunologists
Moscone Center, San Francisco, CA
Booth 307
May 21-25, 2011
CYTO 2011
XXVI Congress of the International Society for Advancement of Cytometry (ISAC)
Baltimore Convention Center, Baltimore, MD
Booth 322
Mass Cytometry: Vaporizing Cells in the Name of Science
Mass cytometry, a technique developed by DVS Sciences, represents a revolutionary spin on classic fluorescence-based flow cytometry. Instead of using antibodies tagged with fluorophores (in which spectral overlap quickly limits the number of parameters available for simultaneous detection), mass cytometry relies on antibodies tagged with transition element isotopes. Antibody-bound cells are vaporized, ionized, and analyzed on a mass spectrometer.



