Sam:LabNotes/Micro-manipulation/2011-4-29
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Non-fixed E.coli cell cryopreservation test using Glycero and Betaine
Objective
- In my test on 04-26-'11 test, I found that using fresh cell is significantly helpful to SYBR-GOLD or DAPI staining. YOYO-staining is not working probably due to the staining method is not optimized well.
- In order to prepare samples for long term usage, I am trying to cryopreserve them in -80C using Bigelow lab protocol.
- Cyropreservation protocol from Bigelow's lab:
Glycerol cryopreservation
- Grew cell over-night (10mL LB borth + spiked in E.coli K-12 strain glycerol stock)x2 tubes
- Next day. Spin down cells at 3000rpm, RT, for 10min. Remove supernatant. Resuspend in 1mL 1X PBS(0.2um-filtered).
- Transfer 100uL suspension into 1.7-mL tubes. Pellet cells at 8000rpm, 5min, RT. Remove supernatant.
- Leave the cell pellet on ice.
- Prepare 50% glycerol in H2O(adding 20mL H2O with 20mL 100% glycerol in a 40mL tube).
- Resuspend cell pellet with 500uL 1X PBS(0.2um-filtered)
- Add 125uL 50% glycerol into the 500uL cell suspension. Repeat pipetting slowly 10X using 1000p tips.
- Store the cell in -80C. Labeled as E.coli + GC.
Betaine cryopreservation
- Prepare following working solution
- 8X TE buffer: Add 4mL 50X TE with 21mL H2O.
- Betaine working sol.: Dissolve 4.8g Betaine with 8mL 8X TE. Filtered the Betaine solution through 0.2um filter.
- (Using the same batch of cell pellet from the test above)Resuspend cell pellet with 500uL 1X PBS(0.2um-filtered).
- Add 71.5uL filtered Betaine solution into the 500uL cell suspension. Repeat pipetting slowly 10X using 1000p tips.
- Store the cell in -80C. Labeled as E.coli + BT.
Validation
- I will compare the cryopreserved cells with fresh cells using my standard DAPI staining protocol.
File:Pos-BF-10X.png File:Pos-DAPI-10X.png File:GC-BF-10X.png File:GC-DAPI-10X.png File:BT-BF-10X.png File:BT-DAPI-10X.png