Apoptosis Notebook
Contents
8-02-2010
8-03-2010
Some test text in bold
We created following tests:
8-04-2010
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8-05-2010
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8-06-2010
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8-07-2010
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8-08-2010
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8-09-2010
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8-10-2010
Transforming competent cells
- eGFP Biobrick: BBa_I714891 SDY_eGFP (Kanamycin)
- TEV recogn N Degron SF3 = pDS7 (Ampicillin)
- TEV p14 recogn = 190-6 (Ampicillin)
-> Protocol: https://www.openwetware.org/wiki/Transforming_chemically_competent_cells_protocol (3 Transformation)
- We added 2 µl DNA
- We plated out 200 µl
Plasmid Isolation
- CMV-Promoter Biobrick: BBa_J52034
-> Protocol: http://www.promega.com/protcards/9fb093/fb093.pdf (4 Plasmid extraction from cells)
- Prepared overnight culture, measured concentration of DNA
-> Poor results -> thrown away
8-11-2010
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8-12-2010
- plasmid extraction of pDS7 (458ng/µl), eGFP (55ng/µl), 190-6 (193ng/µl)
-> Protocol: (4 Plasmid extraktion from cells)
- Restriction digest with EcoRI and PstI in buffer H (for testing DNA is correct)
10µg DNA: pDS7 (2µl), eGFP (15µl), 190-6 (10µl)
-> Protocol: (5 Restriction digest)
- Colony for Plasmidextraktion (CMV, eGFP, pDS7, 190-6) plated
- PhiC31o plated on Ampicillin-Agar, stored at 37°C
- 50% Glycerol made (for the glycerolstock PhiC31o)
8-13-2010
- Agarosegelelectrophoresis with the digestions (CMV, eGFP, pDS7, 190-6), 125V for 30 minutes and then for 20 minutes;
expected DNA bands: 190-6 (4840bp, 1903bp), pDS7 (8027bp, 6bp), CMV (654 bp (Insert), 2079bp (Plasmid)), eGFP (720bp (Insert), 2750bp (Plasmid))
- Correct DNA bands for 190-6 (~4800bp, ~1900bp, ~6700bp (undigested plasmid)) and eGFP (~2000bp (Plasmid), ~750 bp (Insert)); CMV probably not digested (two bands; one probably normal, one supercoiled) and pDS7 not clear
- Restriction digest from CMV (EcoR1, Pst1; 6µl DNA, buffer H) and pDS7 (EcoR1, Spe1; 2µl DNA, buffer B)
Expected DNA bands: CMV see above, pDS7 (3647bp, 3369bp, 1011bp, 6bp)
8-14-2010
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8-15-2010
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8-16-2010
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8-17-2010
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8-18-2010
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8-19-2010
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8-20-2010
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8-21-2010
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8-22-2010
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