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Team:Groningen/Labwork/16 July 2013
From 2013.igem.org
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</table> | </table> | ||
| - | + | <br> Ran the gel 1.5% agarose using the big slots, this posed a couple of problems: | |
| + | <br> The gel was to thick, the slots were still open but the electrophoresis machine needed to be filled up to the brim with 1x KBE buffer. | ||
| + | <br> epje 3. (duplo) opened during the PCR so almost no solution was left. | ||
| + | <br> added 60 uL gene ruler to the first slot, which is way to much. | ||
| + | <br> gel ran ADD 90 V for 45 minutes, started foaming because of to much KBE. | ||
'''Sander''' | '''Sander''' | ||
<br/>did a Restriction digestion for Silk and Signal Sequences. incubation started at 11:00 for the signal sequences and 11:30 for the silk. | <br/>did a Restriction digestion for Silk and Signal Sequences. incubation started at 11:00 for the signal sequences and 11:30 for the silk. | ||
Revision as of 12:24, 16 July 2013
Mirjam
Finally the colonies are growing on LB agar plates with ampicillin. The negative control does not show any colonies, the double negative does??, the positive control shows a lot of red colonies. On one of the four plates there are no colonies present, on two of them only a couple and on one a lot.
The colonies are picked and placed in LB medium with ampicillin to grow further for miniprep.
Inne
Did a PCR with 3 samples in duplo
| Sample | Primer F | Primer R | Annealing temp. |
| 1 | without strep tag | without strep tag | 78 C |
| 2 | with strep tag | without strep tag | 78 C |
| 3 | without strep tag | with strep tag | 80 C |
Protocol:
| amount | compound |
| 28.2 uL | MilliQ |
| 1.5 uL | 5% DMSO |
| 1 uL | each dNTP |
| 10 uL | Phusion GC buffer |
| 2.5 uL | Primer F |
| 2.5 uL | Primer R |
| 1 uL | Silk template BBa_16 |
| 0.3 uL | Phusion polymerase |
Ran the gel 1.5% agarose using the big slots, this posed a couple of problems:
The gel was to thick, the slots were still open but the electrophoresis machine needed to be filled up to the brim with 1x KBE buffer.
epje 3. (duplo) opened during the PCR so almost no solution was left.
added 60 uL gene ruler to the first slot, which is way to much.
gel ran ADD 90 V for 45 minutes, started foaming because of to much KBE.
Sander
did a Restriction digestion for Silk and Signal Sequences. incubation started at 11:00 for the signal sequences and 11:30 for the silk.
