August/8 August 2009
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(New page: Today we carried out the following procedures (in rough chronological order): 1. Checked the cell cultures transformed and plated out yesterday (8/7) for colony formation and made an appr...)
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(New page: Today we carried out the following procedures (in rough chronological order): 1. Checked the cell cultures transformed and plated out yesterday (8/7) for colony formation and made an appr...)
Newer edit →
Revision as of 12:56, 8 August 2009
Today we carried out the following procedures (in rough chronological order):
1. Checked the cell cultures transformed and plated out yesterday (8/7) for colony formation and made an approximate count of the number of colonies.
(plate number)-(location on plate) (no. of colonies)
2-12H none 1-12C none 1-12A none 2-24G none 2-18F none 1-6O ~10 1-10K ~10 1-18L ~10
2. Conducted a 'miniprep' to harvest and check concentration of plasmids from 10 sample. (incubated since yesterday 8/7~) Result of Nanodrop concentration check:
(sample No.) (concentration) [260/280] [260/230]
1-23L 24.9 ng/uL 1.77 1.77 2-16F 36.0 ng/uL 1.77 1.99 1-8O 19.3 ng/uL 1.65 1.59 1-2M 18.4 ng/uL 1.64 2.01 1-19B 40.9 ng/uL 1.56 0.83 2-16H 27.7 ng/uL 1.68 1.38 1-14D 9.3 ng/uL 1.66 2.31 2-8M 9.9 ng/uL 1.65 1.90 2-16M 24.6 ng/uL 1.72 1.24 1-14F 2.5 ng/uL 1.11 0.25 ←× 1-23J ×
3. gel electrophoresis
uL | |
EcoRⅠ | 1 |
SpeⅠ | 1 |
10*Buffer No.2 | 2 |
DNA (EpsE) | 5 |
TOTAL | 20 |
↓
37℃,22hr
↓
× (SYBR Safe : 30min???)