MIT Flow Cytometer Core Facility
From OpenWetWare
(Difference between revisions)
| Line 1: | Line 1: | ||
| - | 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 12:43, 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.


