MIT Flow Cytometer Core Facility: Difference between revisions
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This information is largely gleaned from the [http://web.mit.edu/flowcytometry/www/ Flow Facility Homepage] | {{stub}} | ||
This information is largely gleaned from the [http://web.mit.edu/flowcytometry/www/ Flow Facility Homepage]. As well as conversations with Glenn Paradis. | |||
==Flow Cytometers== | |||
==FACS== | |||
There are 4 cell sorters in the facility: | |||
Excitation Wavelengths | |||
#488,633 | |||
#407,488,633 | |||
#? | |||
#? | |||
There FACS-Aria machines (2 of the 4) have a system for creating the droplet which allows for smaller cells (i.e. bacteria) to be resolved. The MOFLO machines are not as capable in this regard. |
Revision as of 09:43, 31 May 2005
This information is largely gleaned from the Flow Facility Homepage. As well as conversations with Glenn Paradis.
Flow Cytometers
FACS
There are 4 cell sorters in the facility:
Excitation Wavelengths
- 488,633
- 407,488,633
- ?
- ?
There FACS-Aria machines (2 of the 4) have a system for creating the droplet which allows for smaller cells (i.e. bacteria) to be resolved. The MOFLO machines are not as capable in this regard.