Team:Alberta/Notebook

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{{:Team:Alberta/Templates/Header}}
{{:Team:Alberta/Templates/Header}}
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<div class="roundBox">
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<font size=5> &nbsp;&nbsp;&nbsp;iGem Notebook</font>
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</div>
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== iGen Diary ==
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<br/>
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{|align="justify"
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<div class="underline"><font size=5>May</font></div>
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|-
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|May.9-11.2012
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<br/>
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|-
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<font size=3>
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|Rick and Tom recruited and learning basic laboratory protocols, such as making competent cells, restriction digests, cell transformation, gel electrophoresis.
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May.9-11.2012
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|-
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</font>
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|May. 24
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-
|-
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<font size=2>
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|Rick, Tom, Spencer, and Easwar learned how to use PCR today, with varying degrees of success.
+
Rick and Tom began coming in to the lab regularly and started learning basic laboratory protocols, such as making competent cells, restriction digests, cell transformation, gel electrophoresis, ect.
-
|-
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</font>
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|May 31
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-
|-
+
<br/>
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|Today Tom finally managed to get a PCR to work, though it took him about twelve attempts.
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<font size=3>
-
|-
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May. 24
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|June 4
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</font>
-
|-
+
 
-
|Made working stock of puc19 and then transformed Top10 with puc19. Overnight cultures were also set up in preparation for the making of competent cells
+
<font size=2>
-
|-
+
Rick, Tom, Spencer, and Easwar learned how to use PCR today, with varying degrees of success.
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|June 5
+
</font>
-
|-
+
 
-
|Competent cells were made today using a standard procedure which took the entire day.
+
<br/>
-
|-
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<font size=3>
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|June 6
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May 31
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|-
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</font>
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|The competent cells were tested with basic puc19 transformation, and the transformation worked.
+
 
-
|-
+
<font size=2>
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|June 7-8
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Today Tom finally managed to get a PCR to work, though it took him about twelve attempts.
-
|-
+
</font>
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|Today multiple PCRs were run on puc19 with two of the color genes and a C1 gene.
+
 
-
|-
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{|align="right"
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|June 11
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|[[https://2012.igem.org/Team:Alberta/Notebook Top page]]
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|-
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|}
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|Made pUC19 plasmid with the new color genes and C1 and transformed it into cells.
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-
|-
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<br/>
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|June 18-21
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<div class="underline"><font size=5>June</font></div>
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|-
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|We cloned a variety of different (9) promoters into our color gene plasmids, in order to get a sense of relative promoter strengths. we also seqencing those construct to check they are correct
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<br/>
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|-
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<font size=3>
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|June 22- july 3
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June 4
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|-
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</font>
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|We PCR new RBS  colour genes and regulatory promoters. we then made those constructs into kanamycin resistant plasmid backbone and transform them into Top 10 cells.
+
 
-
|-
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<font size=2>
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|July 4-5
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Made working stock of puc19 and then transformed Top10 with puc19. Overnight cultures were also set up in preparation for the making of competent cells
-
|-
+
</font>
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|Torrin and Sarah Join. we perform the same work again on TG1.  
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-
|-
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<br/>
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|July 6
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<font size=3>
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|-
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June 5
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|Tom checked overnights of origin cut site strains and chose colonies to be sequenced.
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</font>
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|-
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|July 9-10
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<font size=2>
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|-
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Competent cells were made today using a standard procedure which took the entire day. The competent cell procedure is described elsewhere in this wiki.
-
|Today Tom Used the successful origin cut site plasmid with Amp Resistance and replaced that resistance with Chlr.
+
</font>
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Torrin and Sarah are creating and testing chemical gradient plates, and learning additional laboratory procedure.
+
 
-
Rick and Spencer is making competent cells of TG1 so that we can test our current parts in an E.Coli strain that grows faster than our current Top10.
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<br/>
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|-
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<font size=3>
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|Rick and Easwar are drop in LacI and Tet R repressor into chloranphenicol construct.
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June 6
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|-
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</font>
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|July 11
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-
|-
+
<font size=2>
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|We continued our experiments with making chemical gradients on agar plates.
+
The competent cells were tested with basic puc19 transformation, and the transformation worked with acceptable efficiency.
-
|-
+
</font>
-
|
+
 
-
|-
+
<br/>
-
|
+
<font size=3>
 +
June 7-8
 +
</font>
 +
 
 +
<font size=2>
 +
Today multiple PCRs were run on puc19 with two of the color genes and a repressor gene.
 +
</font>
 +
 
 +
<br/>
 +
<font size=3>
 +
June 11
 +
</font>
 +
 
 +
<font size=2>
 +
Made pUC19 plasmid with various color genes and C1 and transformed it into cells.
 +
</font>
 +
 
 +
<br/>
 +
<font size=3>
 +
June 18-21
 +
</font>
 +
 
 +
<font size=2>
 +
We cloned a variety of different promoters (nine total) into our color gene plasmids in order to get a sense of relative promoter strengths. We also sent off to sequencing those construct to check that they are correct.
 +
</font>
 +
 
 +
<br/>
 +
<font size=3>
 +
June 22- July 3
 +
</font>
 +
 
 +
<font size=2>
 +
We used PCR to add new RBS  colour genes and regulatory promoters to our constructs. We then pieced those constructs into kanamycin resistant plasmid backbone and transform them into Top 10 cells.
 +
</font>
 +
 
 +
{|align="right"
 +
|[[https://2012.igem.org/Team:Alberta/Notebook Top page]]
 +
|}
 +
 
 +
<br/>
 +
<div class="underline"><font size=5>July</font></div>
 +
 
 +
<br/>
 +
<font size=3>
 +
July 4-5
 +
</font>
 +
 
 +
<font size=2>
 +
Torrin and Sarah join the team. We performed the same work on the TG1 strain of E.Coli as a learning exercise.  
 +
</font>
 +
 
 +
<br/>
 +
<font size=3>
 +
July 6
 +
</font>
 +
 
 +
<font size=2>
 +
Creation of a plasmid with a cut site near the origin of replication began today. This plasmid will be used in order to modify the promoter on the plasmid's origin of replication.
 +
</font>
 +
 
 +
<br/>
 +
<font size=3>
 +
July 9-10
 +
</font>
 +
 
 +
<font size=2>
 +
Today Tom Used the successful origin cut site plasmid with Amp Resistance and replaced that resistance with Chlr.

Latest revision as of 21:56, 18 September 2012

   Team Alberta




   iGem Notebook


May


May.9-11.2012

Rick and Tom began coming in to the lab regularly and started learning basic laboratory protocols, such as making competent cells, restriction digests, cell transformation, gel electrophoresis, ect.


May. 24

Rick, Tom, Spencer, and Easwar learned how to use PCR today, with varying degrees of success.


May 31

Today Tom finally managed to get a PCR to work, though it took him about twelve attempts.

[Top page]


June


June 4

Made working stock of puc19 and then transformed Top10 with puc19. Overnight cultures were also set up in preparation for the making of competent cells


June 5

Competent cells were made today using a standard procedure which took the entire day. The competent cell procedure is described elsewhere in this wiki.


June 6

The competent cells were tested with basic puc19 transformation, and the transformation worked with acceptable efficiency.


June 7-8

Today multiple PCRs were run on puc19 with two of the color genes and a repressor gene.


June 11

Made pUC19 plasmid with various color genes and C1 and transformed it into cells.


June 18-21

We cloned a variety of different promoters (nine total) into our color gene plasmids in order to get a sense of relative promoter strengths. We also sent off to sequencing those construct to check that they are correct.


June 22- July 3

We used PCR to add new RBS colour genes and regulatory promoters to our constructs. We then pieced those constructs into kanamycin resistant plasmid backbone and transform them into Top 10 cells.

[Top page]


July


July 4-5

Torrin and Sarah join the team. We performed the same work on the TG1 strain of E.Coli as a learning exercise.


July 6

Creation of a plasmid with a cut site near the origin of replication began today. This plasmid will be used in order to modify the promoter on the plasmid's origin of replication.


July 9-10

Today Tom Used the successful origin cut site plasmid with Amp Resistance and replaced that resistance with Chlr.

Retrieved from "http://2012.igem.org/Team:Alberta/Notebook"