Team:Newcastle/Labwork/17 September 2009

From 2009.igem.org

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[[Image:Team Newcastle 2009 iGEM ProbationaryP-Sign.PNG|50px|right]]
[[Image:Team Newcastle 2009 iGEM ProbationaryP-Sign.PNG|50px|right]]
=Formal Lab Session - 17th September 2009=
=Formal Lab Session - 17th September 2009=
-
==<u>Stochastic switch team</u>==
+
[[Image:Team Newcastle 2009 iGEM 17-09-09 IMG 1220.JPG|300px|center]]
 +
<br>
 +
=<font color="Orange"><u>Overview</u></font>=
 +
<font color="Orange">
 +
*[[#Stochastic Switch Team|Stochastic Switch Team]] '''- '''
 +
<br>
 +
*[[#Metal Sensor Team|Metal Sensor Team]] '''- '''
 +
<br>
 +
*[[#Sporulation Tuning/Chassis Team|Sporulation Tuning/Chassis Team]] '''- '''
 +
<br>
 +
</font>
 +
<br>
 +
==<u>Stochastic Switch Team</u>==
 +
[[Image:Team Newcastle 2009 iGEM 17-09-09 IMG 1247.JPG|200px|center]]
Today we ran the minipreps for sac and ara transformed cells however- perhaps due to poor miniprep procedure- the sac test digest yeilded poor results, however the ara transformants miniprep gave a ~200bp band along with the backbone in 8/12 lanes:  
Today we ran the minipreps for sac and ara transformed cells however- perhaps due to poor miniprep procedure- the sac test digest yeilded poor results, however the ara transformants miniprep gave a ~200bp band along with the backbone in 8/12 lanes:  
Line 18: Line 31:
[[Image:Team NewcFragpreps1.png]]  
[[Image:Team NewcFragpreps1.png]]  
 +
<br>
-
<center>
+
==<u>Metal Sensor Team</u>==
-
{|cellpadding="10"
+
[[Image:Team Newcastle 2009 iGEM 17-09-09 IMG 1229.JPG|350px|center]]
-
|{{#calendar: title=Team:Newcastle/Labwork |year=2009 | month=07 }}
+
<br>
-
|{{#calendar: title=Team:Newcastle/Labwork |year=2009 | month=08 }}
+
===Introduction===
-
|{{#calendar: title=Team:Newcastle/Labwork |year=2009 | month=09 }}
+
In yesterday's lab session the Metal Sensing team carried out mini-preps on the 12 colonies of potential ''cotC-GFP-smtA'' ''E. coli'' transformants and analysed them. Despite them showing incorrectly sized bands when digested and ran on gel, the team proceded to carry out preparations to midi-prep colony 8 on the basis of consistency of the band patterns and the theory that the digests may not have worked properly. The midi-prep will be done today.
 +
 
 +
The team also prepared to ligate the ''cadA'' promoter to the ''BBa_J33206'' BioBrick (which contains the ''arsR'' gene and ''arsR'' binding site and has the promoter cut out) but only got as far as digesting the two fragments. The cadmium-sensor has been put on hold as of the [https://2009.igem.org/Team:Newcastle/Meetings/16_September_2009 General Meeting on 16/09/09].
 +
 
 +
Additionally the metal sensing team prepared for transformation in ''Bacillus subtilis'' by carrying out the evening steps of the protocol - this will mean that if the midi-preps are a success then ''B. subtilis'' can be transformed with ''cotC-GFP-smtA'' in ''pMUTIN4'' today!
 +
 
 +
Today's lab work will focus on '''midi-prepping colony 8 (which is a potential ''cotC-GFP-smtA'' transformant ''E. coli'' colony)'''. '''The DNA will then be analysed''' by digesting a sample with ''BamHI'' and ''HindIII'' and running it on agarose gel through DNA gel electrophoresis. '''If successful, the DNA will be used to transform ''B. subtilis'' cells'''; if unsuccessful the ligations of ''pMUTIN4'' to ''cotC-GFP-smtA'' will have to be repeated on another day.
 +
<br>
 +
 
 +
===Practical Outline===
 +
[[Image:Team Newcastle 2009 iGEM 17-09-09 IMG 1228.JPG|200px|right]]
 +
The tasks the Metal Sensing team hope to carry out by the end of the day include the following:
 +
<br>
 +
# Midi-prep colony 8 of the potential ''cotC-GFP-smtA'' transformant ''E. coli DH5-alpha'' cells.
 +
# Digest the midi-prepped DNA with ''BamHI'' and ''HindIII''
 +
# Analyse the digested products through DNA gel electrophoresis:
 +
## If successful, use midi-prepped DNA to transform ''Bacillus subtilis''
 +
## If unsuccessful, prepare to carry out a second attempt at ligating ''cotC-GFP-smtA'' to ''pMUTIN4''.
 +
<br>
 +
 
 +
===Procedure===
 +
====1) Midi-prep of potential ''cotC-GFP-smtA'' transformant ''E. coli'' cells====
 +
[[Image:Team Newcastle 2009 iGEM 17-09-09 IMG 1230.JPG|200px|right]]
 +
To carry out the midi-prep we used Sigma-Aldrich's GenElute HP Midi-prep kit (and the [https://2009.igem.org/Team:Newcastle/Project/Labwork/MoreProtocols#Midiprep protocol] attached to it). We conducted steps 1-6 and then steps 7b to 11b (the Spin Method) followed by the DNA concentration step. There was only one major change to the protocol:
 +
<br>
 +
* For the DNA concentration step instead of transferring the eluted DNA to one centrifuge tube, the DNA was transferred into two Eppendorf tubes. This change means that we now have access to a centrifuge capable of reaching 13,000rpm; if we had stuck to using the centrifuge tubes described in the protocol then we wouldn't be able to reach the required g-force.
 +
<br>
 +
Once the midi-prep process was completed the DNA was placed in the -20ºC freezer.
 +
<br>
 +
 
 +
====2) Analysis of midi-prep DNA====
 +
=====a) Quantifying the DNA=====
 +
The midi-prep DNA, which was now stored in two Eppendorf tubes, was then analysed using the NanoDrop spectrophotometer to check for DNA. The concentrations of DNA in the 2 Eppendorf tubes were as follows:
 +
<br>
 +
* Eppendorf tube 1 = 118.9ng/ul
 +
* Eppendorf tube 2 = 100.7ng/ul
 +
<br>
 +
In total, that means we have 219.6ng/ul of plasmid DNA. In the 40ul of solution that means we have 8.784 micrograms of DNA in total. This is sufficient for ''Bacillus subtilis'' transformations.
 +
<br>
 +
 
 +
=====b) Digesting the midi-preps=====
 +
[[Image:Team Newcastle 2009 iGEM 17-09-09 IMG 1254.JPG|200px|right]]
 +
A sample of the midi-prep DNA was then digested with ''BamHI'' and ''HindIII'' restirction enzymes. The contents of the digest reaction were as follows:
 +
<br>
 +
* 10ul of midi-prep DNA
 +
* 1ul of FastDigest ''HindIII'' restriction enzyme
 +
* 1ul of FastDigest ''BamHI'' restriction enzyme
 +
* 2ul of FastDigest 10x restriction buffer
 +
* 6ul of sterile distilled water
 +
<br>
 +
The digests were allowed to run for 1 hour under 37ºC incubation (regulated by water bath)
 +
<br>
 +
 
 +
=====c) DNA gel electrophoresis=====
 +
The digested midi-prep sample was then run on agarose gel in DNA gel electrophoresis - this sample was accompanied by DNA samples from the Sporulation team. The electrophoresis was allowed to commence for 30 minutes under 80 volts to yield the following GelDoc photograph:
 +
<br>
 +
[[Image:Team Newcastle 2009 iGEM Geldoc 2009-09-17 18hr 17min.jpg|400px|center]]
 +
<br>
 +
The sample that our team is interested in is the single sample on the right hand side. This gel photograph shows two clear faults making analysis very difficult and almost impossible:
 +
<br>
 +
# The DNA ''HindIII'' ladder has either degraded or has been made up incorrectly.
 +
# The desired clarity of the bands has not been reached.
 +
<br>
 +
In light of this unsuccessful DNA gel electrophoresis procedure, the Metal Sensing team will have to carry out this task tomorrow with a different DNA ladder and with better-made gel.
 +
<br>
 +
 
 +
====3) ''Bacillus subtilis'' transformations====
 +
Due to the unsuccessful DNA gel electrophoresis, we are unable to determine whether the midi-prep DNA is really the ''cotC'' BioBrick held inside the ''pMUTIN4'' plasmid. Because of this we will have to postpone the ''Bacillus subtilis'' transformations until tomorrow. The overnight cultures, which were set up yesterday, were discarded and fresh overnights were set up according to the [https://2009.igem.org/Team:Newcastle/Project/Labwork/OurProtocols/TransformBac#Evening_before_transformations_day "Evening before transformations" steps] of the ''Bacillus subtilis'' protocol.
 +
<br>
 +
 
 +
==<u>Sporulation Tuning/Chassis Team</u>==
 +
 
 +
===Introduction===
 +
[[Image:Team Newcastle 2009 iGEM 17-09-09 IMG 1249.JPG|200px|right]]
 +
* Good news for yesterday's transformation, both cwlJ + pSB1AT3 and cwlJ + pSB1AT3:sleB did work and we got some colonies on antibiotic plates.
 +
* As a back plan, we did a normal ligation today for transformation.
 +
* Also we digest cwlJ PCR result with EcoRI and SpeI in case we may perform another ligation and transformation.
 +
* Our plan B for double clone is:
 +
<br>
 +
# PCR sleB and cwlJ
 +
# Digest sleB with XbaI
 +
# Digest cwlJ with SpeI
 +
# ligate sleB and cwlJ together
 +
# PCR our ligated cwlJ and sleB with primer cwlJForward and sleBReverse
 +
# Digest PCR result by EcoRI and SpeI and ligate to pSB1AT3
 +
 
 +
<br>
 +
 
 +
===Experiment procedure===
 +
 
 +
==== Digest cwlJ PCR result ====
 +
* The PCR result came from No.5 clean up DNA which was PCRed on day 11/09/09.
 +
* Prepare the digest reaction.
 +
  dd H2O                    7ul
 +
  10X fast digest buffer    7ul
 +
  Fast EcoRI                3ul
 +
  Fast speI                  3ul
 +
  cwlJ DNA                  50ul
 +
  ------------------------------
 +
                            70ul
 +
 
 +
==== Prepare cwlJ and sleB fragment for Plan B====
 +
 
 +
* Prepare buffer mix and Taq
 +
For Go Taq
 +
  Reaction buffer  10ul x 8 = 80ul
 +
            dNTP  2ul x 8 = 16ul
 +
  --------------------------------
 +
                              96ul
 +
  12ul for each reaction
 +
<br>
 +
  GoTaq(5U/ul)  0.25ul x 6 =  1.5ul
 +
  ddH2O                      10.5ul
 +
  ----------------------------------
 +
                                12ul
 +
  2ul for each reaction
 +
 
 +
<br>
 +
     
 +
 
 +
{| border="1"
 +
|+ Exp. PCR experiment for gene cwlJ and sleB
 +
! No. !! Water (ul) !! PCR Mix (ul) !! Forward Primer (ul) !! Reverse Primer (ul) !! Template (ul) !! Polymerase used (ul) !! Total Volume (ul)
 +
|-
 +
| 1 || 29 || 12 || cwlJForward 2.5ul || cwlJReverse 2.5ul  || cwlJ PCR result 2ul || GoTaq 2ul || 50
 +
|-
 +
| 2 || 29 || 12 || cwlJForward 2.5ul || cwlJReverse 2.5ul  || cwlJ PCR result 2ul || GoTaq 2ul|| 50
 +
|-
 +
| 3 || 31 || 12 || cwlJForward 2.5ul  || cwlJReverse 2.5ul || 0 || GoTaq 2ul|| 50
 +
|-
 +
| 4 || 29 || 12 || sleBForward 2.5ul || sleBReverse 2.5ul  || B.Subtilis 168 || GoTaq 2ul || 50
 +
|-
 +
| 5 || 29 || 10 || sleBForward 2.5ul || sleBReverse 2.5ul || B.Subtilis 168  || GoTaq 2ul || 50
 +
|-
 +
| 6 || 31 || 10 || sleBForward 2.5ul || sleBReverse 2.5ul || 0 || BioTaq 2ul || 50
|}
|}
-
</center>
+
<br>
 +
* PCR procedure: STD50
 +
<br>
 +
95C 2min -->[95C 30S --> 50C 30S --> 75C 1min] 30 runs --> 75C 5min --> store at 4C
 +
 
 +
==== Normal Ligation ====
 +
This ligation is a back up for cwlJ transformation.
 +
* L3: Ligation reaction
 +
  dd H2O                    0.5ul
 +
  ligation buffer              2ul
 +
  digested cwlJ              16ul
 +
  digeste pSB1AT3            0.5ul
 +
  T4 ligase                    1ul
 +
  --------------------------------
 +
                              20ul
 +
* L3 control
 +
  dd H2O                    1.5ul
 +
  ligation buffer              2ul
 +
  digested cwlJ              16ul
 +
  digeste pSB1AT3            0.5ul
 +
  --------------------------------
 +
                              20ul
 +
 
 +
* Put the reaction tubes on top shelf of frige overnight.
 +
 
 +
==== Gel extraction ====
 +
[[Image:Team Newcastle 2009 iGEM 17-09-09 IMG 1252.JPG|200px|right]]
 +
* After 1 hour digestion of cwlJ, we purified cwlJ by gel extraction kit alone with two other digested sample (Goksel's and Jess's)
 +
 
 +
==== Culture L1 and L2 transformation cells for Mini Prep ====
 +
* Add 5ml liquid LB+Amp+Tet medium into sterilized glass tube.
 +
* Pick colonies from yesterday's transformation plates.
 +
** No. L1 1--> 12  cwlJ+pSB1AT3 transformation Green Tag
 +
** No. L2 1--> 12  cwlJ + pSB1AT3:sleB transformation Blue Tag
 +
* 37C shake incubator overnight
 +
 
 +
===Conclusion===
 +
* PCR result for cwlJ and sleB
 +
* Gel picture for digested cwlJ and other two sample (Goksel's and Jess's)
 +
 
 +
<br>
 +
[[Image:|400px|center]]
 +
 
 +
===Futher plan===
 +
 
 +
{{:Team:Newcastle/Project/Labwork/CalTemplate}}
{{:Team:Newcastle/Footer}}
{{:Team:Newcastle/Footer}}
{{:Team:Newcastle/Right}}
{{:Team:Newcastle/Right}}

Latest revision as of 14:09, 21 October 2009

Team Newcastle 2009 iGEM ProbationaryP-Sign.PNG

Formal Lab Session - 17th September 2009

Team Newcastle 2009 iGEM 17-09-09 IMG 1220.JPG


Overview

Stochastic Switch Team

Team Newcastle 2009 iGEM 17-09-09 IMG 1247.JPG

Today we ran the minipreps for sac and ara transformed cells however- perhaps due to poor miniprep procedure- the sac test digest yeilded poor results, however the ara transformants miniprep gave a ~200bp band along with the backbone in 8/12 lanes:

Team NewcastleAra 170909.png


Midi prep cultures were set up using cultures corresponding to lanes 1 and 3 for ara.

To test whether the poor sac result was due to the miniprep more miniprep cultures were set up to do tomorrow.

Today also we did fragment preps for Goksels sspb the ara fragment, and a cwlJ fragment for Hanny:

Team NewcFragpreps1.png

Metal Sensor Team

Team Newcastle 2009 iGEM 17-09-09 IMG 1229.JPG


Introduction

In yesterday's lab session the Metal Sensing team carried out mini-preps on the 12 colonies of potential cotC-GFP-smtA E. coli transformants and analysed them. Despite them showing incorrectly sized bands when digested and ran on gel, the team proceded to carry out preparations to midi-prep colony 8 on the basis of consistency of the band patterns and the theory that the digests may not have worked properly. The midi-prep will be done today.

The team also prepared to ligate the cadA promoter to the BBa_J33206 BioBrick (which contains the arsR gene and arsR binding site and has the promoter cut out) but only got as far as digesting the two fragments. The cadmium-sensor has been put on hold as of the General Meeting on 16/09/09.

Additionally the metal sensing team prepared for transformation in Bacillus subtilis by carrying out the evening steps of the protocol - this will mean that if the midi-preps are a success then B. subtilis can be transformed with cotC-GFP-smtA in pMUTIN4 today!

Today's lab work will focus on midi-prepping colony 8 (which is a potential cotC-GFP-smtA transformant E. coli colony). The DNA will then be analysed by digesting a sample with BamHI and HindIII and running it on agarose gel through DNA gel electrophoresis. If successful, the DNA will be used to transform B. subtilis cells; if unsuccessful the ligations of pMUTIN4 to cotC-GFP-smtA will have to be repeated on another day.

Practical Outline

Team Newcastle 2009 iGEM 17-09-09 IMG 1228.JPG

The tasks the Metal Sensing team hope to carry out by the end of the day include the following:

  1. Midi-prep colony 8 of the potential cotC-GFP-smtA transformant E. coli DH5-alpha cells.
  2. Digest the midi-prepped DNA with BamHI and HindIII
  3. Analyse the digested products through DNA gel electrophoresis:
    1. If successful, use midi-prepped DNA to transform Bacillus subtilis
    2. If unsuccessful, prepare to carry out a second attempt at ligating cotC-GFP-smtA to pMUTIN4.


Procedure

1) Midi-prep of potential cotC-GFP-smtA transformant E. coli cells

Team Newcastle 2009 iGEM 17-09-09 IMG 1230.JPG

To carry out the midi-prep we used Sigma-Aldrich's GenElute HP Midi-prep kit (and the protocol attached to it). We conducted steps 1-6 and then steps 7b to 11b (the Spin Method) followed by the DNA concentration step. There was only one major change to the protocol:

  • For the DNA concentration step instead of transferring the eluted DNA to one centrifuge tube, the DNA was transferred into two Eppendorf tubes. This change means that we now have access to a centrifuge capable of reaching 13,000rpm; if we had stuck to using the centrifuge tubes described in the protocol then we wouldn't be able to reach the required g-force.


Once the midi-prep process was completed the DNA was placed in the -20ºC freezer.

2) Analysis of midi-prep DNA

a) Quantifying the DNA

The midi-prep DNA, which was now stored in two Eppendorf tubes, was then analysed using the NanoDrop spectrophotometer to check for DNA. The concentrations of DNA in the 2 Eppendorf tubes were as follows:

  • Eppendorf tube 1 = 118.9ng/ul
  • Eppendorf tube 2 = 100.7ng/ul


In total, that means we have 219.6ng/ul of plasmid DNA. In the 40ul of solution that means we have 8.784 micrograms of DNA in total. This is sufficient for Bacillus subtilis transformations.

b) Digesting the midi-preps
Team Newcastle 2009 iGEM 17-09-09 IMG 1254.JPG

A sample of the midi-prep DNA was then digested with BamHI and HindIII restirction enzymes. The contents of the digest reaction were as follows:

  • 10ul of midi-prep DNA
  • 1ul of FastDigest HindIII restriction enzyme
  • 1ul of FastDigest BamHI restriction enzyme
  • 2ul of FastDigest 10x restriction buffer
  • 6ul of sterile distilled water


The digests were allowed to run for 1 hour under 37ºC incubation (regulated by water bath)

c) DNA gel electrophoresis

The digested midi-prep sample was then run on agarose gel in DNA gel electrophoresis - this sample was accompanied by DNA samples from the Sporulation team. The electrophoresis was allowed to commence for 30 minutes under 80 volts to yield the following GelDoc photograph:

Team Newcastle 2009 iGEM Geldoc 2009-09-17 18hr 17min.jpg


The sample that our team is interested in is the single sample on the right hand side. This gel photograph shows two clear faults making analysis very difficult and almost impossible:

  1. The DNA HindIII ladder has either degraded or has been made up incorrectly.
  2. The desired clarity of the bands has not been reached.


In light of this unsuccessful DNA gel electrophoresis procedure, the Metal Sensing team will have to carry out this task tomorrow with a different DNA ladder and with better-made gel.

3) Bacillus subtilis transformations

Due to the unsuccessful DNA gel electrophoresis, we are unable to determine whether the midi-prep DNA is really the cotC BioBrick held inside the pMUTIN4 plasmid. Because of this we will have to postpone the Bacillus subtilis transformations until tomorrow. The overnight cultures, which were set up yesterday, were discarded and fresh overnights were set up according to the "Evening before transformations" steps of the Bacillus subtilis protocol.

Sporulation Tuning/Chassis Team

Introduction

Team Newcastle 2009 iGEM 17-09-09 IMG 1249.JPG
  • Good news for yesterday's transformation, both cwlJ + pSB1AT3 and cwlJ + pSB1AT3:sleB did work and we got some colonies on antibiotic plates.
  • As a back plan, we did a normal ligation today for transformation.
  • Also we digest cwlJ PCR result with EcoRI and SpeI in case we may perform another ligation and transformation.
  • Our plan B for double clone is:


  1. PCR sleB and cwlJ
  2. Digest sleB with XbaI
  3. Digest cwlJ with SpeI
  4. ligate sleB and cwlJ together
  5. PCR our ligated cwlJ and sleB with primer cwlJForward and sleBReverse
  6. Digest PCR result by EcoRI and SpeI and ligate to pSB1AT3


Experiment procedure

Digest cwlJ PCR result

  • The PCR result came from No.5 clean up DNA which was PCRed on day 11/09/09.
  • Prepare the digest reaction. 
 dd H2O                     7ul
 10X fast digest buffer     7ul
 Fast EcoRI                 3ul
 Fast speI                  3ul
 cwlJ DNA                  50ul
 ------------------------------
                           70ul

Prepare cwlJ and sleB fragment for Plan B

  • Prepare buffer mix and Taq

For Go Taq 

 Reaction buffer  10ul x 8 = 80ul
            dNTP   2ul x 8 = 16ul
 --------------------------------
                             96ul
 12ul for each reaction



 GoTaq(5U/ul)   0.25ul x 6 =  1.5ul
 ddH2O                       10.5ul
 ----------------------------------
                               12ul
 2ul for each reaction



Exp. PCR experiment for gene cwlJ and sleB
No. Water (ul) PCR Mix (ul) Forward Primer (ul) Reverse Primer (ul) Template (ul) Polymerase used (ul) Total Volume (ul)
1 29 12 cwlJForward 2.5ul cwlJReverse 2.5ul cwlJ PCR result 2ul GoTaq 2ul 50
2 29 12 cwlJForward 2.5ul cwlJReverse 2.5ul cwlJ PCR result 2ul GoTaq 2ul 50
3 31 12 cwlJForward 2.5ul cwlJReverse 2.5ul 0 GoTaq 2ul 50
4 29 12 sleBForward 2.5ul sleBReverse 2.5ul B.Subtilis 168 GoTaq 2ul 50
5 29 10 sleBForward 2.5ul sleBReverse 2.5ul B.Subtilis 168 GoTaq 2ul 50
6 31 10 sleBForward 2.5ul sleBReverse 2.5ul 0 BioTaq 2ul 50


  • PCR procedure: STD50


95C 2min -->[95C 30S --> 50C 30S --> 75C 1min] 30 runs --> 75C 5min --> store at 4C

Normal Ligation

This ligation is a back up for cwlJ transformation.

  • L3: Ligation reaction 
 dd H2O                     0.5ul
 ligation buffer              2ul
 digested cwlJ               16ul
 digeste pSB1AT3            0.5ul
 T4 ligase                    1ul
 --------------------------------
                             20ul
  • L3 control 
 dd H2O                     1.5ul
 ligation buffer              2ul
 digested cwlJ               16ul
 digeste pSB1AT3            0.5ul
 --------------------------------
                             20ul
  • Put the reaction tubes on top shelf of frige overnight.

Gel extraction

Team Newcastle 2009 iGEM 17-09-09 IMG 1252.JPG
  • After 1 hour digestion of cwlJ, we purified cwlJ by gel extraction kit alone with two other digested sample (Goksel's and Jess's)

Culture L1 and L2 transformation cells for Mini Prep

  • Add 5ml liquid LB+Amp+Tet medium into sterilized glass tube.
  • Pick colonies from yesterday's transformation plates.
    • No. L1 1--> 12 cwlJ+pSB1AT3 transformation Green Tag
    • No. L2 1--> 12 cwlJ + pSB1AT3:sleB transformation Blue Tag
  • 37C shake incubator overnight

Conclusion

  • PCR result for cwlJ and sleB
  • Gel picture for digested cwlJ and other two sample (Goksel's and Jess's)


[[Image:|400px|center]]

Futher plan

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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