Team:TUDelft/24 August 2009
From 2009.igem.org
(Difference between revisions)
(New page: Transformaltion of friday 21-08-2009 looked good. On each plate there were 80-90 kolonies) |
Danielsoes (Talk | contribs) |
||
Line 1: | Line 1: | ||
+ | {{Template:TUDelftiGEM2009}} | ||
+ | |||
+ | {{Template:TUDelftiGEM2009_LabNotebook}} | ||
+ | |||
+ | ='''24 August 2009'''= | ||
+ | |||
Transformaltion of friday 21-08-2009 looked good. On each plate there were 80-90 kolonies | Transformaltion of friday 21-08-2009 looked good. On each plate there were 80-90 kolonies | ||
+ | |||
+ | ===Daniel=== | ||
+ | |||
+ | Digestion of assemblies in order to do the second round of assembly. | ||
+ | Gel 1% (left) for Calin´s PCR and 2% (right) for my digestions and Calin´s PCR | ||
+ | |||
+ | [[Image:Gel240809.jpg|600px]] | ||
+ | |||
+ | '''Right Gel (2%)''' | ||
+ | |||
+ | {| border="1" align="center" | ||
+ | | Well || Assembly || Expected Plasmid Size || Status | ||
+ | |- align="center" | ||
+ | | 1 || [http://www.eurogentec.com/EGT/Images/RESALES/Electrophoresis/Regular%20DNA%20Ladder/7-SmartLadder.jpg DNA Ladder] || || <font color=limegreen>✔</font> | ||
+ | |- align="center" | ||
+ | | 2 || 4A || 824 || ? | ||
+ | |- align="center" | ||
+ | | 3 || 5A || 1040 || <font color=limegreen>✔</font> | ||
+ | |- align="center" | ||
+ | | 4 || 2A || 214 || ? | ||
+ | |- align="center" | ||
+ | | 5 || 3A || 183 || ? | ||
+ | |- align="center" | ||
+ | | 6 || 1A || 1076 || ? | ||
+ | |- align="center" | ||
+ | | 7 || PCR 1 || || | ||
+ | |- align="center" | ||
+ | | 8 || PCR 2 || || | ||
+ | |- align="center" | ||
+ | | 9 || PCR 3 || || | ||
+ | |- align="center" | ||
+ | | 10 || PCR 4 || || | ||
+ | |- align="center" | ||
+ | | 11 || PCR 5 || || | ||
+ | |- align="center" | ||
+ | | 12 || PCR 6 || || | ||
+ | |} | ||
+ | |||
+ | {{Template:TUDelftiGEM2009_end}} |
Revision as of 16:45, 29 August 2009
Lab Notebook
|
|
|
|
24 August 2009
Transformaltion of friday 21-08-2009 looked good. On each plate there were 80-90 kolonies
Daniel
Digestion of assemblies in order to do the second round of assembly. Gel 1% (left) for Calin´s PCR and 2% (right) for my digestions and Calin´s PCR
Right Gel (2%)
Well | Assembly | Expected Plasmid Size | Status |
1 | [http://www.eurogentec.com/EGT/Images/RESALES/Electrophoresis/Regular%20DNA%20Ladder/7-SmartLadder.jpg DNA Ladder] | ✔ | |
2 | 4A | 824 | ? |
3 | 5A | 1040 | ✔ |
4 | 2A | 214 | ? |
5 | 3A | 183 | ? |
6 | 1A | 1076 | ? |
7 | PCR 1 | ||
8 | PCR 2 | ||
9 | PCR 3 | ||
10 | PCR 4 | ||
11 | PCR 5 | ||
12 | PCR 6 |