Team:Newcastle/Labwork/12 August 2009

From 2009.igem.org

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{{:Team:Newcastle/Header}}
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__NOTOC__
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[[Image:Team Newcastle 2009 iGEM ProbationaryP-Sign.PNG|50px|right]]
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=Formal Lab Session - 12th August 2009=
 +
[[Image:Team Newcastle iGEM 2009 12-08-09 IMG 0386.JPG|thumb|350px|center|The Stochastic Switch team and the Chassis Team discuss ideas with Neil]]
 +
<br>
 +
=<font color="Orange"><u>Overview</u></font>=
 +
<font color="Orange">
 +
*[[#Metal Sensor Team|Metal Sensor Team]] '''- LB + Chloramphenicol plates containing potential ''Bacillus subtilis'' transformants yielded colonies - transformations successful!'''
 +
<br>
 +
*[[#Stochastic Switch Team|Stochastic Switch Team]] '''- attempted to transform ''B. subtilis'' with ''pGFP-rrnB'' as practice'''
 +
<br>
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*[[#Sporulation Tuning/Chassis Team|Sporulation Tuning/Chassis Team]] '''- attempted to recover ''cw1D'' spores using Method A - somewhat successful'''
 +
</font>
 +
<br>
 +
==<u>Metal Sensor Team</u>==
 +
===Recap===
 +
In the last session the Metal Sensing team attempted to transform ''B. subtilis'' with ''pGFP-rrnB'' plasmid (an integration vector). We carried out the procedure and plated the 'transformants' onto 4 plates:
 +
<br>
 +
* LB alone - (MM competence medium MINUS ''B. subtilis'')
 +
* LB + Chloramphenicol - (''Bacillus subtilis'' + water (NO DNA))
 +
* LB + Chloramphenicol - 50ul of ''B. subtilis'' + ''pGFP-rrnB''
 +
* LB + Chloramphenicol - 200ul of ''B. subtilis'' + ''pGFP-rrnB''
 +
<br>
 +
Today, the Metal Sensing team will assess the plates and judge whether the transformations have worked well.
 +
<br>
 +
===Observations===
 +
[[Image:Team Newcastle 2009 iGEM 12-08-09 IMG 0377.JPG|250px]]
 +
[[Image:Team Newcastle 2009 iGEM 12-08-09 IMG 0378.JPG|250px]]
 +
<br>
 +
No colonies grew on the LB alone plate or the LB Chloramphenicol plate with ''B. subtilis'' lacking ''pGFP-rrnB''. However there was considerable growth on both of the LB + Chloramphenicol plates which contained ''pGFP-rrnB'' ''B. subtilis'' transformants - more colonies could be seen in the 200ul portion than on the 50ul portion but that is simply down to concentration of cells. Both transformations were a success, as can be seen in the above photograph.
-
=Lab Session 12/08/09=
 
==<u>Stochastic Switch Team</u>==
==<u>Stochastic Switch Team</u>==
-
Today we are trying to transform ''Bacillus subtilis'' with gfp-rrnb integration vector. Metal sensor team kindly inoculated ''B. subtilis'' cells into flask tubes and placed them into the shaking incubator. We labelled them as 1,2,3 and control.
+
[[Image:Team Newcastle iGEM 2009 12-08-09 IMG 0380.JPG|thumb|200px|Goksel and Jess are all prepared for the ''Bacillus subtilis'' transformation procedure with these solutions made up]]
 +
Today we are trying to transform ''Bacillus subtilis'' with ''pGFP-rrnB'' integration vector. Metal sensor team kindly inoculated ''B. subtilis'' cells into flask tubes and placed them into the shaking incubator. We labelled them as 1,2,3 and control.
We prepared four plates
We prepared four plates
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*The cultures were plated out using glass beads and put in the 37 incubator.
*The cultures were plated out using glass beads and put in the 37 incubator.
 +
<br>
==<u>Sporulation Tuning/Chassis Team</u>==
==<u>Sporulation Tuning/Chassis Team</u>==
-
Today, we made our first attempt to recover the cwlD spores which were kindly sent to us by Anne Moir from Sheffield University as mentioned on the 4th of August.
+
Today, we made our first attempt to recover the <i>cwlD</i> spores which were kindly sent to us by Anne Moir from Sheffield University as mentioned on the 4th of August.
 +
 
 +
[[Image:Newcastle 12 August Jane Pipette.jpg|thumb|200px|center|Jane pipetting the cwlD spores out of the eppendorf tubes]]
 +
 
We used the protocol for [https://2009.igem.org/Team:Newcastle/Project/Labwork/MoreProtocols#Recovery_of_cwlD_spores Method A] as mentioned.
We used the protocol for [https://2009.igem.org/Team:Newcastle/Project/Labwork/MoreProtocols#Recovery_of_cwlD_spores Method A] as mentioned.
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===Preparation===
===Preparation===
-
The [https://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/7_August_2009&action=edit&section=5 Lysozyme Stock Solution] was made on the [https://2009.igem.org/Team:Newcastle/Labwork/7_August_2009 7th of August].
+
The [https://2009.igem.org/Team:Newcastle/Labwork/7_August_2009#Preparation Lysozyme Stock Solution] was made on the [https://2009.igem.org/Team:Newcastle/Labwork/7_August_2009 7th of August].
 +
 
====L-alanine====
====L-alanine====
-
 
We need:
We need:
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We made 0.03L (30ml) of 0.05M L-alanine which we filter sterilised.
We made 0.03L (30ml) of 0.05M L-alanine which we filter sterilised.
 +
 +
[[Image:Newcastle 12 August L-Alanine Filter Sterilise.jpg|165px|Filter Sterilising the L-Alanine.]]
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[[Image:Newcastle 12 August L-Alanine Filter Sterilise 1.jpg|165px|Filter Sterilising the L-Alanine.]]
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[[Image:Newcastle 12 August L-Alanine Filter Sterilise 2.jpg|165px|Filter Sterilising the L-Alanine.]]
The amount of powdered L-alanine needed to make 30ml of 0.05M L-alanine solution is:
The amount of powdered L-alanine needed to make 30ml of 0.05M L-alanine solution is:
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Therefore, 800ul of buffer solution requires 32ul of lysozyme stock solution.
Therefore, 800ul of buffer solution requires 32ul of lysozyme stock solution.
 +
 +
;Note: Due to previous calculation errors, only 4ul of stock lysozyme was added to a ml of buffer solution. Instead, 40ml of stock lysozyme should have been added. As lysozyme is added to disrupt the bacterial cell wall, 4ul may not have been sufficient.
 +
The experiment was performed again on [https://2009.igem.org/Team:Newcastle/Labwork/17_August_2009 Monday, 17th August]. See [https://2009.igem.org/Team:Newcastle/Labwork/17_August_2009 Monday, 17th August] for more details.
===Protocol===
===Protocol===
 +
In addition to the protocol for [https://2009.igem.org/Team:Newcastle/Project/Labwork/MoreProtocols#Recovery_of_cwlD_spores Method A], it is important to take note of the following points:
*10ul of cwlD spores were added into the lysozyme and buffer solution.
*10ul of cwlD spores were added into the lysozyme and buffer solution.
 +
 +
[[Image:Newcastle 12 August cwlD 37 Degree Incubator.jpg|thumb|200px|center|The spores in the 37 degree incubator.]]
*After the addition of L-alanine to the solution, which would supposedly initiate germination, the solution was left in the incubator for 10 minutes
*After the addition of L-alanine to the solution, which would supposedly initiate germination, the solution was left in the incubator for 10 minutes
*After 10 minutes, the eppendorf tube containing the solution was spinned down for approximately 1 minute.
*After 10 minutes, the eppendorf tube containing the solution was spinned down for approximately 1 minute.
**Note: Fill another eppendorf tube with water and put it on the opposite site to balance out the weight.
**Note: Fill another eppendorf tube with water and put it on the opposite site to balance out the weight.
*The supernatant was removed from the eppendorf tube and the spores were resuspended in 1000ul of LB solution.
*The supernatant was removed from the eppendorf tube and the spores were resuspended in 1000ul of LB solution.
 +
 +
;Note: The team faced difficulties in resuspending the spores.
 +
 +
 +
[[Image:Newcastle 12 August cwlD Serial Dilutions.jpg|thumb|200px|center|The serial dilutions.]]
 +
*A serial dilution was performed as illustrated below, and 50ul of each solution was plated out using glass beads on LB + Cm plates.
*A serial dilution was performed as illustrated below, and 50ul of each solution was plated out using glass beads on LB + Cm plates.
*In addition, 5ul of the cwlD spores were plated out using glass beads on LB + Cm plates. No colonies should grow on this plate as the spores were not treated.
*In addition, 5ul of the cwlD spores were plated out using glass beads on LB + Cm plates. No colonies should grow on this plate as the spores were not treated.
===Results===
===Results===
 +
The following pictures shows the results for the recovery of the cwlD spores.
 +
 +
As mentioned, due to previous calculation errors, only 4ul of stock lysozyme was added to a ml of buffer solution in this experiment. A volume of 40ml of stock lysozyme should have been added instead.
 +
As lysozyme is added to disrupt the bacterial cell wall, 4ul may not have been sufficient, resulting in no or few colonies growing on the plates, as seen in the pictures below.
 +
The experiment was performed again on [https://2009.igem.org/Team:Newcastle/Labwork/17_August_2009 Monday, 17th August]. See [https://2009.igem.org/Team:Newcastle/Labwork/17_August_2009 Monday, 17th August] for more details.
 +
 +
 +
In this plate, 5ul of spores were directly plated on without going through any treatment to see if any colonies grew.
 +
 +
[[Image:Newcastle 14 August cwlD plate notreat.jpg|250px|center|thumb|cwlD mutant plate, without treatment.]]
 +
 +
 +
The spores in this plate were not diluted, thus it is expected that the number of colonies growing in this plate would be greater than the other plates. 
 +
 +
[[Image:Newcastle 14 August cwlD plate 1.jpg|250px|center|thumb|cwlD mutant plate, concentration = 1]]
 +
 +
 +
Only one colony is seen growing on this plate, where a 1 time dilution was performed.
 +
 +
[[Image:Newcastle 14 August cwlD plate 101.jpg|250px|center|thumb|cwlD mutant plate, concentration = 10<sup>-1</sup>]]
 +
 +
 +
As can been seen in the following pictures, starting from the 2 times dilution onwards, no colonies can be seen growing.
 +
 +
[[Image:Newcastle 14 August cwlD plate 102.jpg|250px|center|thumb|cwlD mutant plate, concentration = 10<sup>-2</sup>]]
 +
 +
[[Image:Newcastle 14 August cwlD plate 103.jpg|250px|center|thumb|cwlD mutant plate, concentration = 10<sup>-3</sup>]]
 +
 +
[[Image:Newcastle 14 August cwlD plate 104.jpg|250px|center|thumb|cwlD mutant plate, concentration = 10<sup>-4</sup>]]
 +
 +
[[Image:Newcastle 14 August cwlD plate 105.jpg|250px|center|thumb|cwlD mutant plate, concentration = 10<sup>-5</sup>]]
 +
 +
{{:Team:Newcastle/Project/Labwork/CalTemplate}}
{{:Team:Newcastle/Footer}}
{{:Team:Newcastle/Footer}}
{{:Team:Newcastle/Right}}
{{:Team:Newcastle/Right}}

Latest revision as of 14:15, 20 October 2009

Team Newcastle 2009 iGEM ProbationaryP-Sign.PNG

Formal Lab Session - 12th August 2009

The Stochastic Switch team and the Chassis Team discuss ideas with Neil


Overview

  • Metal Sensor Team - LB + Chloramphenicol plates containing potential Bacillus subtilis transformants yielded colonies - transformations successful!




Metal Sensor Team

Recap

In the last session the Metal Sensing team attempted to transform B. subtilis with pGFP-rrnB plasmid (an integration vector). We carried out the procedure and plated the 'transformants' onto 4 plates:

  • LB alone - (MM competence medium MINUS B. subtilis)
  • LB + Chloramphenicol - (Bacillus subtilis + water (NO DNA))
  • LB + Chloramphenicol - 50ul of B. subtilis + pGFP-rrnB
  • LB + Chloramphenicol - 200ul of B. subtilis + pGFP-rrnB


Today, the Metal Sensing team will assess the plates and judge whether the transformations have worked well.

Observations

Team Newcastle 2009 iGEM 12-08-09 IMG 0377.JPG Team Newcastle 2009 iGEM 12-08-09 IMG 0378.JPG
No colonies grew on the LB alone plate or the LB Chloramphenicol plate with B. subtilis lacking pGFP-rrnB. However there was considerable growth on both of the LB + Chloramphenicol plates which contained pGFP-rrnB B. subtilis transformants - more colonies could be seen in the 200ul portion than on the 50ul portion but that is simply down to concentration of cells. Both transformations were a success, as can be seen in the above photograph.

Stochastic Switch Team

Goksel and Jess are all prepared for the Bacillus subtilis transformation procedure with these solutions made up

Today we are trying to transform Bacillus subtilis with pGFP-rrnB integration vector. Metal sensor team kindly inoculated B. subtilis cells into flask tubes and placed them into the shaking incubator. We labelled them as 1,2,3 and control.

We prepared four plates

  • LB + Bsubtilis (+ Control, cells should grow on this plate)
  • LB + CHL + B. subtilis (- control, cells will not grow on this plate)
  • LB + CHL + B. subtilis + plasmid DNA(Cells should transform with the DNA)
  • LB + CHL + B. subtilis + diluted plasmid DNA (Cells should transform with the DNA)
  • 2xcompetence medium and 2xstravation medium were prepared.
  • We used the 2nd and the 3rd tubes for the tests
  • Incubated the samplesfor three hours at 37C
  • Added the starvation medium and incubated for another 2 hours
  • For each of the two cultures, added 0.4ml of the final solution from the culture and 10ul of DNA into an eppendorf tube.
  • Placed the tubes in the shaking incubator for an hour. To do this we taped the tubes to the base of the incubator. N.B- Chris in the lab swapped the temperatures of the incubators, so we used the one that is opposite the -80 freezer. The starter overnight cultures are also in this incubator -these are labelled 1,2,3 control (we used 2 and 3).
  • The cultures were plated out using glass beads and put in the 37 incubator.


Sporulation Tuning/Chassis Team

Today, we made our first attempt to recover the cwlD spores which were kindly sent to us by Anne Moir from Sheffield University as mentioned on the 4th of August.

Jane pipetting the cwlD spores out of the eppendorf tubes


We used the protocol for Method A as mentioned.

Preparation

The Lysozyme Stock Solution was made on the 7th of August.

L-alanine

We need: 

10mM L-alanine
0.01M L-alanine

We made 0.03L (30ml) of 0.05M L-alanine which we filter sterilised.

Filter Sterilising the L-Alanine. Filter Sterilising the L-Alanine. Filter Sterilising the L-Alanine.

The amount of powdered L-alanine needed to make 30ml of 0.05M L-alanine solution is: 

MW * Desired Volume (L) * Desired Molarity (M) 
89.09* 0.03L * 0.05M = 0.134g

Our final solution volume inclusive of L-alanine is desired to be 1ml. Therefore, the amount of L-alanine stock solution to add, such that the final concentration of L-alanine is 0.01M is: 

0.05M (Stock solution) / 0.01M (Desired Molarity) = 5
In order to obtain a solution with a final concentration of 0.01M,
the stock solution needs to be diluted 5 times.
Desired volume = 1ml
1000ul / 5 = 200ul

200ul of L-alanine stock solution should be added to the buffer and lysozyme solution to make up approximately 1ml. 


Final Volume = 1ml
Volume of buffer solution = 1000ul - 200ul = 800ul
Since 1ml of buffer solution requires 40ul of lysozyme stock solution,
800ul / 1000ul = 0.8
0.8 * 40ul = 32ul

Therefore, 800ul of buffer solution requires 32ul of lysozyme stock solution.

Note
Due to previous calculation errors, only 4ul of stock lysozyme was added to a ml of buffer solution. Instead, 40ml of stock lysozyme should have been added. As lysozyme is added to disrupt the bacterial cell wall, 4ul may not have been sufficient.

The experiment was performed again on Monday, 17th August. See Monday, 17th August for more details.

Protocol

In addition to the protocol for Method A, it is important to take note of the following points:

  • 10ul of cwlD spores were added into the lysozyme and buffer solution.
The spores in the 37 degree incubator.
  • After the addition of L-alanine to the solution, which would supposedly initiate germination, the solution was left in the incubator for 10 minutes
  • After 10 minutes, the eppendorf tube containing the solution was spinned down for approximately 1 minute.
    • Note: Fill another eppendorf tube with water and put it on the opposite site to balance out the weight.
  • The supernatant was removed from the eppendorf tube and the spores were resuspended in 1000ul of LB solution.
Note
The team faced difficulties in resuspending the spores.


The serial dilutions.
  • A serial dilution was performed as illustrated below, and 50ul of each solution was plated out using glass beads on LB + Cm plates.
  • In addition, 5ul of the cwlD spores were plated out using glass beads on LB + Cm plates. No colonies should grow on this plate as the spores were not treated.

Results

The following pictures shows the results for the recovery of the cwlD spores.

As mentioned, due to previous calculation errors, only 4ul of stock lysozyme was added to a ml of buffer solution in this experiment. A volume of 40ml of stock lysozyme should have been added instead. As lysozyme is added to disrupt the bacterial cell wall, 4ul may not have been sufficient, resulting in no or few colonies growing on the plates, as seen in the pictures below. The experiment was performed again on Monday, 17th August. See Monday, 17th August for more details.


In this plate, 5ul of spores were directly plated on without going through any treatment to see if any colonies grew.

cwlD mutant plate, without treatment.


The spores in this plate were not diluted, thus it is expected that the number of colonies growing in this plate would be greater than the other plates.

cwlD mutant plate, concentration = 1


Only one colony is seen growing on this plate, where a 1 time dilution was performed.

cwlD mutant plate, concentration = 10-1


As can been seen in the following pictures, starting from the 2 times dilution onwards, no colonies can be seen growing.

cwlD mutant plate, concentration = 10-2
cwlD mutant plate, concentration = 10-3
cwlD mutant plate, concentration = 10-4
cwlD mutant plate, concentration = 10-5
July
MTWTFSS
    [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/1_July_2009&action=edit 1] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/2_July_2009&action=edit 2] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/3_July_2009&action=edit 3] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/4_July_2009&action=edit 4] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/5_July_2009&action=edit 5]
[http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/6_July_2009&action=edit 6] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/7_July_2009&action=edit 7] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/8_July_2009&action=edit 8] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/9_July_2009&action=edit 9] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/10_July_2009&action=edit 10] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/11_July_2009&action=edit 11] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/12_July_2009&action=edit 12]
[http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/13_July_2009&action=edit 13] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/14_July_2009&action=edit 14] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/15_July_2009&action=edit 15] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/16_July_2009&action=edit 16] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/17_July_2009&action=edit 17] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/18_July_2009&action=edit 18] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/19_July_2009&action=edit 19]
[http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/20_July_2009&action=edit 20] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/21_July_2009&action=edit 21] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/22_July_2009&action=edit 22] [http://2009.igem.org/Team:Newcastle/Labwork/23_July_2009 23] [http://2009.igem.org/Team:Newcastle/Labwork/24_July_2009 24] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/25_July_2009&action=edit 25] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/26_July_2009&action=edit 26]
[http://2009.igem.org/Team:Newcastle/Labwork/27_July_2009 27] [http://2009.igem.org/Team:Newcastle/Labwork/28_July_2009 28] [http://2009.igem.org/Team:Newcastle/Labwork/29_July_2009 29] [http://2009.igem.org/Team:Newcastle/Labwork/30_July_2009 30] [http://2009.igem.org/Team:Newcastle/Labwork/31_July_2009 31]
August
MTWTFSS
          [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/1_August_2009&action=edit 1] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/2_August_2009&action=edit 2]
[http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/3_August_2009&action=edit 3] [http://2009.igem.org/Team:Newcastle/Labwork/4_August_2009 4] [http://2009.igem.org/Team:Newcastle/Labwork/5_August_2009 5] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/6_August_2009&action=edit 6] [http://2009.igem.org/Team:Newcastle/Labwork/7_August_2009 7] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/8_August_2009&action=edit 8] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/9_August_2009&action=edit 9]
[http://2009.igem.org/Team:Newcastle/Labwork/10_August_2009 10] [http://2009.igem.org/Team:Newcastle/Labwork/11_August_2009 11] [http://2009.igem.org/Team:Newcastle/Labwork/12_August_2009 12] [http://2009.igem.org/Team:Newcastle/Labwork/13_August_2009 13] [http://2009.igem.org/Team:Newcastle/Labwork/14_August_2009 14] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/15_August_2009&action=edit 15] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/16_August_2009&action=edit 16]
[http://2009.igem.org/Team:Newcastle/Labwork/17_August_2009 17] [http://2009.igem.org/Team:Newcastle/Labwork/18_August_2009 18] [http://2009.igem.org/Team:Newcastle/Labwork/19_August_2009 19] [http://2009.igem.org/Team:Newcastle/Labwork/20_August_2009 20] [http://2009.igem.org/Team:Newcastle/Labwork/21_August_2009 21] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/22_August_2009&action=edit 22] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/23_August_2009&action=edit 23]
[http://2009.igem.org/Team:Newcastle/Labwork/24_August_2009 24] [http://2009.igem.org/Team:Newcastle/Labwork/25_August_2009 25] [http://2009.igem.org/Team:Newcastle/Labwork/26_August_2009 26] [http://2009.igem.org/Team:Newcastle/Labwork/27_August_2009 27] [http://2009.igem.org/Team:Newcastle/Labwork/28_August_2009 28] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/29_August_2009&action=edit 29] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/30_August_2009&action=edit 30]
[http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/31_August_2009&action=edit 31]
September
MTWTFSS
  [http://2009.igem.org/Team:Newcastle/Labwork/1_September_2009 1] [http://2009.igem.org/Team:Newcastle/Labwork/2_September_2009 2] [http://2009.igem.org/Team:Newcastle/Labwork/3_September_2009 3] [http://2009.igem.org/Team:Newcastle/Labwork/4_September_2009 4] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/5_September_2009&action=edit 5] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/6_September_2009&action=edit 6]
[http://2009.igem.org/Team:Newcastle/Labwork/7_September_2009 7] [http://2009.igem.org/Team:Newcastle/Labwork/8_September_2009 8] [http://2009.igem.org/Team:Newcastle/Labwork/9_September_2009 9] [http://2009.igem.org/Team:Newcastle/Labwork/10_September_2009 10] [http://2009.igem.org/Team:Newcastle/Labwork/11_September_2009 11] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/12_September_2009&action=edit 12] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/13_September_2009&action=edit 13]
[http://2009.igem.org/Team:Newcastle/Labwork/14_September_2009 14] [http://2009.igem.org/Team:Newcastle/Labwork/15_September_2009 15] [http://2009.igem.org/Team:Newcastle/Labwork/16_September_2009 16] [http://2009.igem.org/Team:Newcastle/Labwork/17_September_2009 17] [http://2009.igem.org/Team:Newcastle/Labwork/18_September_2009 18] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/19_September_2009&action=edit 19] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/20_September_2009&action=edit 20]
[http://2009.igem.org/Team:Newcastle/Labwork/21_September_2009 21] [http://2009.igem.org/Team:Newcastle/Labwork/22_September_2009 22] [http://2009.igem.org/Team:Newcastle/Labwork/23_September_2009 23] [http://2009.igem.org/Team:Newcastle/Labwork/24_September_2009 24] [http://2009.igem.org/Team:Newcastle/Labwork/25_September_2009 25] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/26_September_2009&action=edit 26] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/27_September_2009&action=edit 27]
[http://2009.igem.org/Team:Newcastle/Labwork/28_September_2009 28] [http://2009.igem.org/Team:Newcastle/Labwork/29_September_2009 29] [http://2009.igem.org/Team:Newcastle/Labwork/30_September_2009 30]
October
MTWTFSS
      [http://2009.igem.org/Team:Newcastle/Labwork/1_October_2009 1] [http://2009.igem.org/Team:Newcastle/Labwork/2_October_2009 2] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/3_October_2009&action=edit 3] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/4_October_2009&action=edit 4]
[http://2009.igem.org/Team:Newcastle/Labwork/5_October_2009 5] [http://2009.igem.org/Team:Newcastle/Labwork/6_October_2009 6] [http://2009.igem.org/Team:Newcastle/Labwork/7_October_2009 7] [http://2009.igem.org/Team:Newcastle/Labwork/8_October_2009 8] [http://2009.igem.org/Team:Newcastle/Labwork/9_October_2009 9] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/10_October_2009&action=edit 10] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/11_October_2009&action=edit 11]
[http://2009.igem.org/Team:Newcastle/Labwork/12_October_2009 12] [http://2009.igem.org/Team:Newcastle/Labwork/13_October_2009 13] [http://2009.igem.org/Team:Newcastle/Labwork/14_October_2009 14] [http://2009.igem.org/Team:Newcastle/Labwork/15_October_2009 15] [http://2009.igem.org/Team:Newcastle/Labwork/16_October_2009 16] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/17_October_2009&action=edit 17] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/18_October_2009&action=edit 18]
[http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/19_October_2009&action=edit 19] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/20_October_2009&action=edit 20] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/21_October_2009&action=edit 21] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/22_October_2009&action=edit 22] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/23_October_2009&action=edit 23] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/24_October_2009&action=edit 24] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/25_October_2009&action=edit 25]
[http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/26_October_2009&action=edit 26] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/27_October_2009&action=edit 27] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/28_October_2009&action=edit 28] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/29_October_2009&action=edit 29] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/30_October_2009&action=edit 30] [http://2009.igem.org/wiki/index.php?title=Team:Newcastle/Labwork/31_October_2009&action=edit 31]



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