Sam:LabNotes/Micro-manipulation/2011-4-15: Difference between revisions
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>Sam Chiang |
>Sam Chiang |
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===Test of adding final washing with PBTw=== | ===Test of adding final washing with PBTw=== | ||
*Started from the DAPI-stained sample on 4-14-'11 | |||
#Separate the sample into two tubes(250uL/tube) | |||
#Pellet stained cells at 8000rpm, 5min, RT. | |||
#Prepare the PBTw (PBS containing 0.1% Tween20) by adding 40uL Tween20 into 40mL PBS(0.2um filtered). | |||
#Pick up one of the samples. Using 1mL PBTw to wash cells twice. Resuspend the cell pellet in 250uL PBTw. Label the tube as "washed". | |||
#Label the other tube as "non-washed". | |||
==Results== | ==Results== |
Revision as of 01:23, 16 April 2011
Single E.coli cell micromanipulation test on 04-15-'11
Objective
- Further improve the DAPI staining protocol
Experiment design
- Test the following conditions:
- The effect of filtering the fixed E.coli (by 5um-filter)
- Washing and resuspend in PBTw to remove background.
- Using higher amount of DAPI dye.
Procedures
Test of pre-filtering the EtOH-fixed samples
- Starting with EtOH fixed cell (stored in -80C) x2
This cell are about 100uL of OD600=1.0 E.coli, fixed in 500uL 100% EtOH for 3hr.
- Pellet at 5min, 8000 rpm. Wash 1X in 1mL PBS(0.2um-filtered).
- One of the samples was filtered through 5um-filter, and labeled as "F".
- The other one was labeled as "R" following the regular procedure.
- Resuspend in 0.5 mL PBS(0.2um-filtered). Transfer sample in a 1.7mL amber tube.
- Prepare DAPI working solution (5mg/mL -> 1/5 dilution with H2O to 1mg/mL).
- Add DAPI working solution in the E.coli
- Add 1uL dye for "R" tube. Add 4uL dye for the "F" tube.
- Incubate in on the rocking plate/Eppendorf rocking incubator at RT (25C), 400rpm for 15min.
Test of adding final washing with PBTw
- Started from the DAPI-stained sample on 4-14-'11
- Separate the sample into two tubes(250uL/tube)
- Pellet stained cells at 8000rpm, 5min, RT.
- Prepare the PBTw (PBS containing 0.1% Tween20) by adding 40uL Tween20 into 40mL PBS(0.2um filtered).
- Pick up one of the samples. Using 1mL PBTw to wash cells twice. Resuspend the cell pellet in 250uL PBTw. Label the tube as "washed".
- Label the other tube as "non-washed".
Results
Comparisons of different conditions on DAPI-stained E.coli File:Sam 041511-DAPI ecoli 10X-BF-annoated.png File:Sam 041511-DAPI ecoli 10X-DAPI-annoated.png
Discussion
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