Team:Stockholm/11 October 2010
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Revision as of 12:49, 14 October 2010 by AndreasConstantinou (Talk | contribs)
Contents |
Andreas
Removal of insertion in BioBrick suffixes
Plasmid prep
From 8/10 stored pellet
- 50 μl elution buffer.
DNA concentration | ||
---|---|---|
Sample | Conc [ng/μl] | A260/A280 |
pSB1C3.SOD | 163.1 | 1.94 |
Digestion
pSB1C3. SOD | |
---|---|
10X FastDigest buffer | 2 |
DNA (1 μg) | 12.3 |
dH2O | 3.7 |
FD EcoRI | 1 |
FD SpeI | 1 |
20 μl |
- Incubation: 37 °C, 30 min
Gel verification
1 % agarose, 140 V
Expected bands
- Vector: 2175 bp
- Insert: 495 bp
Results
Band slightly larger than expected, but this may also be due to bound restriction enzymes and/or other disturbances. Proceeded to gel extraction.
Gel extraction
Digested pSB1C3.SOD separated on 1 % agarose gel at 110 V, 17 μl sample volume. SOD band extracted and DNA, as well as DNA from samples stored in -20 °C 7/10, were purified using the E.Z.N.A. Gel Extraction kit.
DNA measurements extremely low, but proceeded to ligation/cloning anyway.