Team:TUDelft/5 August 2009
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='''5 August 2009'''= | ='''5 August 2009'''= | ||
+ | ===Sriram=== | ||
+ | Today I did the restiction along with Daniel. After lot of calculation and discussion we did it successfully. Then I prepared a gel and loaded all the restricted samples in the gel and it could be seen in below image: | ||
+ | |||
+ | [[Image:igemdelay060809.jpg|thumb|center|450px]] | ||
+ | |||
+ | Then we decided to continue the assembly tomorrow. Daniel gave me the instruction and he decided to check with how to do the GFP expression experiments. | ||
===Tim Weenink=== | ===Tim Weenink=== | ||
- | [[Image:Tim050809.png| | + | [[Image:Tim050809.png|center|400px]] |
+ | |||
+ | |||
+ | [[Image:Tim050809!Dandcalin.png|center|400px]] | ||
+ | |||
+ | |||
+ | {| border="1" align="center" | ||
+ | | Well || Part || Expected Plasmid Size || Status | ||
+ | |- align="center" | ||
+ | | 1-8 || !D PCR products (wrong primer) || 1100 || <font color=red>✖</font> | ||
+ | |- align="center" | ||
+ | | 9 || [http://www.eurogentec.com/EGT/Images/RESALES/Electrophoresis/Regular%20DNA%20Ladder/7-SmartLadder.jpg DNA Ladder] || || <font color=limegreen>✔</font> | ||
+ | |- align="center" | ||
+ | | 10 || pSB1AK3 linear || 3864 || <font color=limegreen>✔</font> | ||
+ | |- align="center" | ||
+ | | 11 || pSB4C5 linear || 3896 || <font color=limegreen>✔</font> | ||
+ | |- align="center" | ||
+ | | 12 || strong promoter || 2983 || <font color=limegreen>✔</font> | ||
+ | |- align="center" | ||
+ | | 13 || oriT-R linear || ? || <font color=limegreen>✔</font> | ||
+ | |} | ||
+ | |||
+ | ===Orr=== | ||
+ | Prepared 1 liter of LB medium, and helped Calin with the Conjugation procedure. | ||
+ | |||
+ | ===Calin=== | ||
+ | |||
+ | Made test plate for Trimpethoprim. | ||
+ | |||
+ | Ran conjugation test with R751 (TRI) as donor and DH5 α cells with GFP plasmid and AMP as recipients. | ||
+ | |||
+ | Ran three conjugations in parallel, with a conjugation time of 1 hour. | ||
+ | |||
+ | Starting OD for recipients 0.502, for donors 0.542. | ||
+ | |||
+ | Made a total of 40 plates: | ||
+ | |||
+ | |||
+ | {| border="1" align="center" | ||
+ | |- | ||
+ | | <b>Set 1</b> | ||
+ | |- align="center" | ||
+ | | Plate ID || Antibiotics || Dilution || | ||
+ | |- align="center" | ||
+ | | D1 || TRI || 10<sup>0</sup> || | ||
+ | |- align="center" | ||
+ | | D2 || TRI || 10<sup>-2</sup>|| | ||
+ | |- align="center" | ||
+ | | D3 || TRI || 10<sup>-4</sup>|| | ||
+ | |- align="center" | ||
+ | | D4 || TRI || 10<sup>-5</sup>|| | ||
+ | |- align="center" | ||
+ | | D5 || TRI || 10<sup>-6</sup>|| | ||
+ | |- align="center" | ||
+ | | T1 || TRI + AMP || 10<sup>0</sup> || | ||
+ | |- align="center" | ||
+ | | T2 || TRI + AMP || 10<sup>-1</sup>|| | ||
+ | |- align="center" | ||
+ | | T3 || TRI + AMP || 10<sup>-2</sup>|| | ||
+ | |- align="center" | ||
+ | | T4 || TRI + AMP || 10<sup>-3</sup>|| | ||
+ | |- align="center" | ||
+ | | T5 || TRI + AMP || 10<sup>-4</sup>|| | ||
+ | |- align="center" | ||
+ | | T6 || TRI + AMP || 10<sup>-5</sup> || | ||
+ | |- align="center" | ||
+ | | T7 || TRI + AMP || 10<sup>-6</sup>|| | ||
+ | |- align="center" | ||
+ | | R1 || AMP || 10<sup>0</sup> || | ||
+ | |- align="center" | ||
+ | | R2 || AMP || 10<sup>-4</sup>|| | ||
+ | |- align="center" | ||
+ | | R3 || AMP || 10<sup>-5</sup>|| | ||
+ | |- align="center" | ||
+ | | R4 || AMP || 10<sup>-6</sup>|| | ||
+ | |} | ||
+ | <br><br> | ||
+ | {| border="1" align="center" | ||
+ | |- | ||
+ | | <b>Set 2</b> | ||
+ | |- align="center" | ||
+ | | Plate ID || Antibiotics || Dilution || | ||
+ | |- align="center" | ||
+ | | D6 || TRI || 10<sup>0</sup> || | ||
+ | |- align="center" | ||
+ | | D7 || TRI || 10<sup>-2</sup>|| | ||
+ | |- align="center" | ||
+ | | D8 || TRI || 10<sup>-4</sup>|| | ||
+ | |- align="center" | ||
+ | | D9 || TRI || 10<sup>-5</sup>|| | ||
+ | |- align="center" | ||
+ | | D10 || TRI || 10<sup>-6</sup>|| | ||
+ | |- align="center" | ||
+ | | T8 || TRI + AMP || 10<sup>0</sup> || | ||
+ | |- align="center" | ||
+ | | T9 || TRI + AMP || 10<sup>-1</sup>|| | ||
+ | |- align="center" | ||
+ | | T10 || TRI + AMP || 10<sup>-2</sup>|| | ||
+ | |- align="center" | ||
+ | | T11 || TRI + AMP || 10<sup>-3</sup>|| | ||
+ | |- align="center" | ||
+ | | T12 || TRI + AMP || 10<sup>-4</sup>|| | ||
+ | |- align="center" | ||
+ | | T13 || TRI + AMP || 10<sup>-5</sup> || | ||
+ | |- align="center" | ||
+ | | T14 || TRI + AMP || 10<sup>-6</sup>|| | ||
+ | |} | ||
- | + | <br><br> | |
+ | {| border="1" align="center" | ||
+ | |- | ||
+ | | <b>Set 3</b> | ||
+ | |- align="center" | ||
+ | | Plate ID || Antibiotics || Dilution || | ||
+ | |- align="center" | ||
+ | | D11 || TRI || 10<sup>0</sup> || | ||
+ | |- align="center" | ||
+ | | D12 || TRI || 10<sup>-2</sup>|| | ||
+ | |- align="center" | ||
+ | | D13 || TRI || 10<sup>-4</sup>|| | ||
+ | |- align="center" | ||
+ | | D14 || TRI || 10<sup>-5</sup>|| | ||
+ | |- align="center" | ||
+ | | D15 || TRI || 10<sup>-6</sup>|| | ||
+ | |- align="center" | ||
+ | | T15 || TRI + AMP || 10<sup>0</sup> || | ||
+ | |- align="center" | ||
+ | | T16 || TRI + AMP || 10<sup>-1</sup>|| | ||
+ | |- align="center" | ||
+ | | T17 || TRI + AMP || 10<sup>-2</sup>|| | ||
+ | |- align="center" | ||
+ | | T18 || TRI + AMP || 10<sup>-3</sup>|| | ||
+ | |- align="center" | ||
+ | | T19 || TRI + AMP || 10<sup>-4</sup>|| | ||
+ | |- align="center" | ||
+ | | T20 || TRI + AMP || 10<sup>-5</sup> || | ||
+ | |- align="center" | ||
+ | | T21 || TRI + AMP || 10<sup>-6</sup>|| | ||
+ | |} | ||
{{Template:TUDelftiGEM2009_end}} | {{Template:TUDelftiGEM2009_end}} |
Latest revision as of 08:40, 20 October 2009
Lab Notebook
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5 August 2009
Sriram
Today I did the restiction along with Daniel. After lot of calculation and discussion we did it successfully. Then I prepared a gel and loaded all the restricted samples in the gel and it could be seen in below image:
Then we decided to continue the assembly tomorrow. Daniel gave me the instruction and he decided to check with how to do the GFP expression experiments.
Tim Weenink
Well | Part | Expected Plasmid Size | Status |
1-8 | !D PCR products (wrong primer) | 1100 | ✖ |
9 | [http://www.eurogentec.com/EGT/Images/RESALES/Electrophoresis/Regular%20DNA%20Ladder/7-SmartLadder.jpg DNA Ladder] | ✔ | |
10 | pSB1AK3 linear | 3864 | ✔ |
11 | pSB4C5 linear | 3896 | ✔ |
12 | strong promoter | 2983 | ✔ |
13 | oriT-R linear | ? | ✔ |
Orr
Prepared 1 liter of LB medium, and helped Calin with the Conjugation procedure.
Calin
Made test plate for Trimpethoprim.
Ran conjugation test with R751 (TRI) as donor and DH5 α cells with GFP plasmid and AMP as recipients.
Ran three conjugations in parallel, with a conjugation time of 1 hour.
Starting OD for recipients 0.502, for donors 0.542.
Made a total of 40 plates:
Set 1 | |||
Plate ID | Antibiotics | Dilution | |
D1 | TRI | 100 | |
D2 | TRI | 10-2 | |
D3 | TRI | 10-4 | |
D4 | TRI | 10-5 | |
D5 | TRI | 10-6 | |
T1 | TRI + AMP | 100 | |
T2 | TRI + AMP | 10-1 | |
T3 | TRI + AMP | 10-2 | |
T4 | TRI + AMP | 10-3 | |
T5 | TRI + AMP | 10-4 | |
T6 | TRI + AMP | 10-5 | |
T7 | TRI + AMP | 10-6 | |
R1 | AMP | 100 | |
R2 | AMP | 10-4 | |
R3 | AMP | 10-5 | |
R4 | AMP | 10-6 |
Set 2 | |||
Plate ID | Antibiotics | Dilution | |
D6 | TRI | 100 | |
D7 | TRI | 10-2 | |
D8 | TRI | 10-4 | |
D9 | TRI | 10-5 | |
D10 | TRI | 10-6 | |
T8 | TRI + AMP | 100 | |
T9 | TRI + AMP | 10-1 | |
T10 | TRI + AMP | 10-2 | |
T11 | TRI + AMP | 10-3 | |
T12 | TRI + AMP | 10-4 | |
T13 | TRI + AMP | 10-5 | |
T14 | TRI + AMP | 10-6 |
Set 3 | |||
Plate ID | Antibiotics | Dilution | |
D11 | TRI | 100 | |
D12 | TRI | 10-2 | |
D13 | TRI | 10-4 | |
D14 | TRI | 10-5 | |
D15 | TRI | 10-6 | |
T15 | TRI + AMP | 100 | |
T16 | TRI + AMP | 10-1 | |
T17 | TRI + AMP | 10-2 | |
T18 | TRI + AMP | 10-3 | |
T19 | TRI + AMP | 10-4 | |
T20 | TRI + AMP | 10-5 | |
T21 | TRI + AMP | 10-6 |