McClean: Fixation of Yeast (P. Xu Protocol): Difference between revisions
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*Incubate the tube at room temperature for 15-20 minutes. | *Incubate the tube at room temperature for 15-20 minutes. | ||
*Spin down at 8000rpm for 1 minute. | *Spin down at 8000rpm for 1 minute. | ||
*Wash cells with 1X PBS 3 times, spin at 8000rpm for 1 minute each time (can be longer if you need). | *Wash cells with ice cold 1X PBS 3 times, spin at 8000rpm for 1 minute each time (can be longer if you need). | ||
*Resuspend cell pellet in 100ul of 1X PBS. | *Resuspend cell pellet in 100ul of 1X PBS. | ||
*Store samples at 4°C until you are ready to image. | *Store samples at 4°C until you are ready to image. |
Revision as of 12:46, 25 July 2013
Overview
This is the protocol used by P. Xu for fixing yeast cells for GFP fluorescence.
Materials
- Yeast cells
- Formaldehyde 37% (Sigma-Aldrich, #252549)
- Phosphate buffered saline??
Protocol
- Prepare eppendorf tubes with 50μL of 37% formaldehyde, one per sample.
- Add 450μL of culture to 50μL of formaldehyde in an eppendorf tube and mix by inversion. (The goal is to have a final concentration of formaldehyde around 3.7%. So you can adjust the cell and formaldehyde volumes accordingly, as long as you end up with 3.7% formaldehyde).
- Incubate the tube at room temperature for 15-20 minutes.
- Spin down at 8000rpm for 1 minute.
- Wash cells with ice cold 1X PBS 3 times, spin at 8000rpm for 1 minute each time (can be longer if you need).
- Resuspend cell pellet in 100ul of 1X PBS.
- Store samples at 4°C until you are ready to image.
Notes
Please feel free to post comments, questions, or improvements to this protocol. Please sign your name to your note by adding '''*~~~~''': to the beginning of your tip.
References
Contact
Ping Xu 3:12, 25 July 2013 (EDT)
or instead, discuss this protocol.