McGill/October

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<table style="
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font-family: Verdana, Arial, Helvetica, sans-serif;
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vertical-align:middle;
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text-align:center;
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background-color:white;
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border-color:#FFFFFF;
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color:black;
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<tr>
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<td colspan="7" style="font-weight: bold;
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width:170px;
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height:24px;
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color: black;">[[McGill/Team_2:_Repressilator#October_2007|October 2007]]</td>
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</tr>
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<tr>
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<td>M</td>
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<td>Tu</td>
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<td>W</td>
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<td>Th</td>
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<td>F</td>
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<td>Sa</td>
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<td>Su</td>
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</tr>
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<tr>
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<td>[[McGill/Team_2:_Repressilator#October_1|1]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_2|2]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_3|3]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_4|4]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_5|5]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_6|6]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_7|17]]</td>
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</tr>
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<tr>
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<td>[[McGill/Team_2:_Repressilator#October_8|8]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_9|9]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_10|10]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_11|11]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_12|12]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_13|13]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_14|14]]</td>
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</tr>
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<tr>
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<td>[[McGill/Team_2:_Repressilator#October_15|15]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_16|16]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_17|17]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_18|18]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_19|19]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_20|20]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_21|21]]</td>
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</tr>
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<tr>
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<td>[[McGill/Team_2:_Repressilator#October_22|22]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_23|23]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_24|24]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_25|25]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_26|26]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_27|27]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_28|28]]</td>
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</tr>
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<tr>
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<td>[[McGill/Team_2:_Repressilator#October_29|29]]</td>
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<td>[[McGill/Team_2:_Repressilator#October_30|30]]</td>
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</tr></table>
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</td></tr>
== October 2007 ==
== October 2007 ==
-
===October 5===
 
-
Jimmy and I midiprepped 50mL of each E0434 & I5611 using Annette's procedure. Could not prep more because 1. annette's procedure required the clinical centrigue where there are only 6 spots for 15ml tubes, 2.there were not enough sterile epi tubes, 3. could not use <b>real</b> Qiagen procedure instead (the rotor we needed in the big centrifuge is broken). I'm not sure about the yield of this. definitely check the dna conc before screening. one of the last steps in annette's procedure involving the pooling of pellets of DNA from 6 epi tubes to 1 tube using ethanol is iffy and there may be a lot of dna loss there.  
+
===October 1===
 +
Seeded E0434 and I5611 in 1X LB.
-
I've lysated the pellet from another 50mL of each (w/P1) and froze it in case we want to do this again. It has green tape around it. The 2 epi tubes w/ the midi are next to it and also have green tape around them, in the top right corner of the freezer.
+
===October 2===
 +
Diluted E0434 and I5611 a total of 15X in 1X LB. <br>
 +
4.5ml LB (1x)<br>
 +
300ul culture<br>
 +
E0434 - 5ul Amp/Kan, I5611 - 5ul Amp
 +
===October 3===
 +
Did the 15X dilution again as the total volume was not enough to perform a midiprep...stupid me! (Avi).<br>
 +
- Want 200ml of dilution in total in order to allow the culture to grow efficiently overnight.<br>
 +
<u>E0434</u><br>
 +
100ml, 100ml LB 2X, 1.5ml Kan, 200ul Amp, 2ml culture<br>
 +
<u>I5611</u><br>
 +
100ml, 100ml LB 2X, 200ul Amp, 2ml culture
 +
 +
===October 5===
 +
Jimmy and I midiprepped 50mL of each E0434 & I5611 using Annette's procedure. Could not prep more because 1. annette's procedure required the clinical centrifugue where there are only 6 spots for 15ml tubes, 2.there were not enough sterile epi tubes, 3. could not use <b>real</b> Qiagen procedure instead (the rotor we needed in the big centrifuge is broken). I'm not sure about the yield of this. definitely check the dna conc before screening. one of the last steps in annette's procedure involving the pooling of pellets of DNA from 6 epi tubes to 1 tube using ethanol is iffy and there may be a lot of dna loss there.
 +
 +
I've lysated the pellet from another 50mL of each (w/P1) and froze it in case we want to do this again. It has green tape around it. The 2 epi tubes w/ the midi are next to it and also have green tape around them, in the top right corner of the freezer.
Horia
Horia
 +
 +
===October 9===
 +
Screening digest of Horia's midiprep:<br>
 +
<u>E0434</u><br>
 +
1) Xba + SpeI - cuts at 3181bp & 925 bp<br>
 +
2) HindIII + PstI - cuts at 2.8kb & 1.3kb<br>
 +
3) EcoRI - 4.1kb<br>
 +
 +
<u>I5611</u><br>
 +
1) Xba + PstII - cuts at 4.2kb & 2.1kb<br>
 +
2) EcoRI + BsrGI - cuts at 4.1kb & 2.2kb<br>
 +
3) EcoRI - 6.3kb<br>
 +
 +
===October 10===
 +
Screen again as gel had too much EtBr, so bands could not be seen.
 +
 +
===October 11===
 +
Screening was done again, this time it was concluded that there was no DNA in the midiprep, so the midiprep was done incorrectly, or no DNA was salvaged. Ahhh! Taking a break from this cursed lab and waiting for that darned I-brick to show up!

Latest revision as of 03:26, 26 October 2007

October 2007
M Tu W Th F Sa Su
1 2 3 4 5 6 17
8 9 10 11 12 13 14
15 16 17 18 19 20 21
22 23 24 25 26 27 28
29 30

</td></tr>

Contents

October 2007

October 1

Seeded E0434 and I5611 in 1X LB.

October 2

Diluted E0434 and I5611 a total of 15X in 1X LB.
4.5ml LB (1x)
300ul culture
E0434 - 5ul Amp/Kan, I5611 - 5ul Amp

October 3

Did the 15X dilution again as the total volume was not enough to perform a midiprep...stupid me! (Avi).
- Want 200ml of dilution in total in order to allow the culture to grow efficiently overnight.
E0434
100ml, 100ml LB 2X, 1.5ml Kan, 200ul Amp, 2ml culture
I5611
100ml, 100ml LB 2X, 200ul Amp, 2ml culture

October 5

Jimmy and I midiprepped 50mL of each E0434 & I5611 using Annette's procedure. Could not prep more because 1. annette's procedure required the clinical centrifugue where there are only 6 spots for 15ml tubes, 2.there were not enough sterile epi tubes, 3. could not use real Qiagen procedure instead (the rotor we needed in the big centrifuge is broken). I'm not sure about the yield of this. definitely check the dna conc before screening. one of the last steps in annette's procedure involving the pooling of pellets of DNA from 6 epi tubes to 1 tube using ethanol is iffy and there may be a lot of dna loss there.

I've lysated the pellet from another 50mL of each (w/P1) and froze it in case we want to do this again. It has green tape around it. The 2 epi tubes w/ the midi are next to it and also have green tape around them, in the top right corner of the freezer. Horia

October 9

Screening digest of Horia's midiprep:
E0434
1) Xba + SpeI - cuts at 3181bp & 925 bp
2) HindIII + PstI - cuts at 2.8kb & 1.3kb
3) EcoRI - 4.1kb

I5611
1) Xba + PstII - cuts at 4.2kb & 2.1kb
2) EcoRI + BsrGI - cuts at 4.1kb & 2.2kb
3) EcoRI - 6.3kb

October 10

Screen again as gel had too much EtBr, so bands could not be seen.

October 11

Screening was done again, this time it was concluded that there was no DNA in the midiprep, so the midiprep was done incorrectly, or no DNA was salvaged. Ahhh! Taking a break from this cursed lab and waiting for that darned I-brick to show up!

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