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From 2012.igem.org

Contents 1 Morning: Cell counting and sampling 1.1 Protocol: None 2 Afternoon: Cell lysates 2.1 Protocol: None

Morning: Cell counting and sampling

Cell counting

Given our cell density we used a 12x dilution (table). We transfered 6 samples of cells into a 96 well plate, added Trypan blue and analysed each sample with Countess.

[table with results]

Western Blot sampling

Protocol (add to separate page):

1. Centrifugation of the cell samples at 2500xg for 10min. Discard the supernatant (vacuum).
2. Washing: Resuspend the pellet in PBS1x, centrifuge at 2500xg for 10min, discard supernatant.
3. Add at least 1mL PER-M Reagent for 100mg (~100µl) of cell pellet. Pipette up and down to suspend.
4. Shake gently for 10min.
5. Remove cell bedris by centrifugation: ~1400xg for 15min
6. Transfer the supernatant into new tubes for analysis or storage.

• Samples where taken from odd numbered tubes : 1,3,5,7.
• We used 300µl of M-PER Reagent based on the size of our pellets.
• Maximum centrifugation was 10'600xg.

Comments

For samples 3 and 5 we had to repeat step 5 (centrifugation to remove cell debris) because the cell pellet got aspired in the pipette while trying to transfer the supernantant into fresh tubes.

Afternoon: Cell lysates

We prepared cell lysates for future mRNA sampling and for analysing fluorescence the same day. Protocol: Sampling for Tecan machine (add on separate page)

1. Take ~1mio cells in 750 µl PBS
2. Centriguge samples at 450xg for 5min
3. Remove the supernatant (vaccum)
4. Resuspend in 200µl of 1% TritonX in PBS
5. Load onto black well and leave on the shaker for 1 hour.
6. Read fluorescence on Tecan machine

Protocol: Sampling for mRNA (add on separate page)

1. Take ~1mio cells in 750 µl PBS
2. Centriguge samples at 450xg for 5min
3. Remove the supernatant (vaccum) leaving 50µl.
4. Vortex and resuspend.
5. Add 1µl PBS, vortex again.
6. Centrifuge at 450xg for 5min
7. Remove supernatant (pipette) and freeze in liquid nitrogen. Store at -20°C.

Comments