Team:Newcastle/Labwork/31 July 2009

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__NOTOC__
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[[Image:Team Newcastle 2009 iGEM ProbationaryP-Sign.PNG|50px|right]]
 +
=Formal Lab Session - 31st July 2009=
 +
[[Image:Team Newcastle 2009 iGEM 31-07-09 IMG 0231.JPG|250px|center]]
-
=Lab Session 31/07/2009=
 
-
==Previously==
+
==Introduction==
-
''cinR'' ([http://partsregistry.org/Part:BBa_C0077 BBa_C0077]) and ''cinI'' ([http://partsregistry.org/Part:BBa_C0076 BBa_C0076]) coding sequences did not grow in LB + Kan media but they grew in plain LB media. We had overnight cultures prepared for CinR sensitive promoter([http://partsregistry.org/Part:BBa_R0077 BBa_R0077]), ''cI'' coding sequence([http://partsregistry.org/Part:BBa_B1002 BBa_B1002]) and the double terminator([http://partsregistry.org/Part:BBa_B1002 BBa_B1002]).
+
Over the past week we have attempted to transform five BioBricks from the Spring Distributions. Of these BioBricks, ''E. coli'' plus ''cinR'' ([http://partsregistry.org/Part:BBa_C0077 BBa_C0077]) and ''E. coli'' + ''cinI'' ([http://partsregistry.org/Part:BBa_C0076 BBa_C0076]) have not seemed to grow on LB + kan plates suggesting problems with transforming in ''JM109'' cells. With this scenario, we attempted one final transformation but this time using ''DH5-alpha'' ''E. coli'' cells.
-
==Today's Aims==
+
However ''JM109'' ''E. coli'' transformations with the ''CinR'' sensitive promoter([http://partsregistry.org/Part:BBa_R0077 BBa_R0077]), ''cI'' coding sequence([http://partsregistry.org/Part:BBa_B1002 BBa_C0056]) and the double terminator([http://partsregistry.org/Part:BBa_B1002 BBa_B1002]) have all worked and grown on LB + amp plates. Three colonies from each set of BioBrick transformants were then used to inoculate 9 x 5ml LB tubes and allowed to grow overnight.
-
We will do a midi prep for the overnight cultures. We will follow the protocol from GenElute ([http://www.sigmaaldrich.com/etc/medialib/docs/Sigma/Bulletin/na0200bul.Par.0001.File.tmp/na0200bul.pdf NA0200S_NA0200]). The list of plasmid kits can be accessed from [http://www.sigmaaldrich.com/life-science/molecular-biology/dna-and-rna-purification/hp-plasmid-kits.html Gen Elute's plasmid kits page].
+
-
To transfer the binding column, we used two epindorfs for each culture. The volume of the epindorfs were 450ul and we used 45ul of sodium acetate buffer and 315ul of isopropanol for "DNa concentration" step. We centrifuged the tubes at 18000rpm for 30 minutes before adding ethanol to rinse the DNAs. We then centriguged the tubes again for 20 minutes at 13000rpm. If we had used the other machine we would centrifuge the tubes at 18000rpm for 10 minutes. Since it was a slower machine, we used 20 minutes instead.
+
Today's lab session will see us make a decision on BioBricks ''BBa_C0077'' and ''BBa_C0076'' based on whether our final transformation attempt has worked. Today's lab session will also see the team carry out midi-preps from the inoculated LB tubes (one set of three tubes inoculated with ''BBa_C0056'', another set of three tubes inoculated with ''BBa_B1002'' and the final set of three tubes inoculated with ''BBa_R0077'').
-
At the end we air-dried the pellets until the ethanol evaporated. We then added 50ul of PCR water to each epindorf tube and mixed the solution well. Two epindorf tubes with the same colony were combined.
+
==Practical Outline==
 +
[[Image:Team Newcastle 2009 iGEM 31-07-09 IMG 0227.JPG|200px|thumb|right]]
 +
Here are the objectives for today:
 +
<br>
 +
# Carry out midi-preps on ''E. coli'' cultures containing ''BBa_C0056'', ''BBa_B1002'' and ''BBa_R0077''
 +
# Check LB and LB + kan plates for any ''DH5-alpha'' cells transformed with ''BBa_C0077'' and ''BBa_C0076''
 +
## If unsuccessful, abandon,
 +
## If successful, prepare 5ml LB inoculations
 +
<br>
-
Finally we measured the concentration of the DNA in the tubes using spectrometer. We used a sensitive pipet to wash the machine wth 2ul of water twice. We then loaded and measured the concentration for each tube. Between the steps we cleaned the machine with tissues. At the end we loaded with water again for a final cleaning procedure. Results for each tube are as below:
+
==Procedures==
 +
===1) Midi-preps of ''BBa_C0056'', ''BBa_B1002'', and ''BBa_R0077''===
 +
=====Protocol=====
 +
[[Image:Team Newcastle 2009 iGEM 31-07-09 IMG 0229.JPG|200px|thumb|Jess tipping off the supernatant after spinning the overnight cultures in the centrifuge]]
 +
We did a midi prep for the overnight cultures. We followed the protocol from GenElute ([http://www.sigmaaldrich.com/etc/medialib/docs/Sigma/Bulletin/na0200bul.Par.0001.File.tmp/na0200bul.pdf NA0200S_NA0200]). The list of plasmid kits can be accessed from [http://www.sigmaaldrich.com/life-science/molecular-biology/dna-and-rna-purification/hp-plasmid-kits.html Gen Elute's plasmid kits page].
 +
=====Procedure=====
 +
To transfer the binding column, we used two eppendorf tubes for each culture. The volume of the eppendorfs were 450ul and we used 45ul of sodium acetate buffer and 315ul of isopropanol for "DNA concentration" step. We centrifuged the tubes at 18000rpm for 30 minutes before adding ethanol to rinse the DNAs. We then centriguged the tubes again for 20 minutes at 13000rpm. If we had used the faster machine we would centrifuge the tubes at 18000rpm for 10 minutes. Since it was a slower machine, we used 20 minutes instead.
-
After ethanol  
+
At the end we air-dried the pellets until the ethanol evaporated. We then added 50ul of PCR water to each eppendorf tube and mixed the solution well. Two eppendorf tubes from the same colony were combined.
 +
=====Results=====
 +
[[Image:Team Newcastle 2009 iGEM 31-07-09 IMG 0237.JPG|200px|thumb|Goksel adding one of the agents needed for the plasmid midiprep]]
 +
Finally we measured the concentration of the DNA in the tubes using spectrometer. We used a sensitive pipet to wash the machine wth 2ul of water twice.  We then loaded and measured the concentration for each tube. Between the steps we cleaned the machine with tissues. At the end we loaded with water again for a final cleaning procedure.
 +
 +
Tubes with plasmid DNAs were then placed to the -20C freezer.
 +
 +
Results for each tube are as below.
 +
 +
<br>
 +
=====Results for BBa_C0056=====
 +
We had high DNA concentration for the first tube.
 +
 +
The concentration of DNA: 124.6 ng/uL
 +
The ratio of DNA concentration to protein concentration(260/280): 1.84
 +
The ratio of protein concentration to RNA concentration(260/230): 1.73
 +
 +
[[Image:Team_Newcastle_iGEM_2009_31-07-09_no_1.JPG|550px]]
 +
 +
=====Results for BBa_B1002 =====
 +
We had low DNA concentration for the second tube.
 +
 +
The concentration of DNA: 28.3 ng/uL
 +
The ratio of DNA concentration to protein concentration(260/280): 1.66
 +
The ratio of protein concentration to RNA concentration(260/230): 1.13
 +
 +
[[Image:Team_Newcastle_iGEM_2009_31-07-09_no_2.JPG|550px]]
 +
 +
=====Results for BBa_R0077=====
 +
The concentration of DNA: 53.8 ng/uL
 +
The ratio of DNA concentration to protein concentration(260/280): 1.75
 +
The ratio of protein concentration to RNA concentration(260/230): 1.39
 +
 +
[[Image:Team_Newcastle_iGEM_2009_31-07-09_no_3.JPG|550px]]
 +
<br>
 +
===2) ''BBa_C0077'' and ''BBa_C0076'' Transformants ===
 +
[[Image:Team Newcastle 2009 iGEM 31-07-09 IMG 0225.JPG|425px|center]]
 +
<br>
 +
At last, colonies were found on the plates which contained ''DH5-alpha'' transformed with ''BBa_C0077'' and ''BBa_c0076''! The 2 LB-alone plates for both ''BBa_C0077'' and ''BBa_C0076'' transformants  was completely covered in a lawn of bacteria. The LB + kan plate with the ''DH5-alpha'' cells transformed with ''BBa_C0077'' yielded about 5 colonies whereas the LB + kan plate with the ''BBa_C0076'' transformants yielded 100+ colonies.
 +
 +
However the plates will be stored in the fridge, over the weekend, for LB inoculations and future mini-preps to take place later (hopefully in Monday's lab session).
 +
 +
{{:Team:Newcastle/Project/Labwork/CalTemplate}}
{{:Team:Newcastle/Footer}}
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Latest revision as of 17:26, 17 October 2009


Team Newcastle 2009 iGEM ProbationaryP-Sign.PNG

Formal Lab Session - 31st July 2009

Team Newcastle 2009 iGEM 31-07-09 IMG 0231.JPG


Introduction

Over the past week we have attempted to transform five BioBricks from the Spring Distributions. Of these BioBricks, E. coli plus cinR ([http://partsregistry.org/Part:BBa_C0077 BBa_C0077]) and E. coli + cinI ([http://partsregistry.org/Part:BBa_C0076 BBa_C0076]) have not seemed to grow on LB + kan plates suggesting problems with transforming in JM109 cells. With this scenario, we attempted one final transformation but this time using DH5-alpha E. coli cells.

However JM109 E. coli transformations with the CinR sensitive promoter([http://partsregistry.org/Part:BBa_R0077 BBa_R0077]), cI coding sequence([http://partsregistry.org/Part:BBa_B1002 BBa_C0056]) and the double terminator([http://partsregistry.org/Part:BBa_B1002 BBa_B1002]) have all worked and grown on LB + amp plates. Three colonies from each set of BioBrick transformants were then used to inoculate 9 x 5ml LB tubes and allowed to grow overnight.

Today's lab session will see us make a decision on BioBricks BBa_C0077 and BBa_C0076 based on whether our final transformation attempt has worked. Today's lab session will also see the team carry out midi-preps from the inoculated LB tubes (one set of three tubes inoculated with BBa_C0056, another set of three tubes inoculated with BBa_B1002 and the final set of three tubes inoculated with BBa_R0077).

Practical Outline

Team Newcastle 2009 iGEM 31-07-09 IMG 0227.JPG

Here are the objectives for today:

  1. Carry out midi-preps on E. coli cultures containing BBa_C0056, BBa_B1002 and BBa_R0077
  2. Check LB and LB + kan plates for any DH5-alpha cells transformed with BBa_C0077 and BBa_C0076
    1. If unsuccessful, abandon,
    2. If successful, prepare 5ml LB inoculations


Procedures

1) Midi-preps of BBa_C0056, BBa_B1002, and BBa_R0077

Protocol
Jess tipping off the supernatant after spinning the overnight cultures in the centrifuge

We did a midi prep for the overnight cultures. We followed the protocol from GenElute ([http://www.sigmaaldrich.com/etc/medialib/docs/Sigma/Bulletin/na0200bul.Par.0001.File.tmp/na0200bul.pdf NA0200S_NA0200]). The list of plasmid kits can be accessed from [http://www.sigmaaldrich.com/life-science/molecular-biology/dna-and-rna-purification/hp-plasmid-kits.html Gen Elute's plasmid kits page].

Procedure

To transfer the binding column, we used two eppendorf tubes for each culture. The volume of the eppendorfs were 450ul and we used 45ul of sodium acetate buffer and 315ul of isopropanol for "DNA concentration" step. We centrifuged the tubes at 18000rpm for 30 minutes before adding ethanol to rinse the DNAs. We then centriguged the tubes again for 20 minutes at 13000rpm. If we had used the faster machine we would centrifuge the tubes at 18000rpm for 10 minutes. Since it was a slower machine, we used 20 minutes instead.

At the end we air-dried the pellets until the ethanol evaporated. We then added 50ul of PCR water to each eppendorf tube and mixed the solution well. Two eppendorf tubes from the same colony were combined.

Results
Goksel adding one of the agents needed for the plasmid midiprep

Finally we measured the concentration of the DNA in the tubes using spectrometer. We used a sensitive pipet to wash the machine wth 2ul of water twice. We then loaded and measured the concentration for each tube. Between the steps we cleaned the machine with tissues. At the end we loaded with water again for a final cleaning procedure.

Tubes with plasmid DNAs were then placed to the -20C freezer.

Results for each tube are as below.


Results for BBa_C0056

We had high DNA concentration for the first tube.

The concentration of DNA: 124.6 ng/uL
The ratio of DNA concentration to protein concentration(260/280): 1.84
The ratio of protein concentration to RNA concentration(260/230): 1.73

Team Newcastle iGEM 2009 31-07-09 no 1.JPG

Results for BBa_B1002

We had low DNA concentration for the second tube.

The concentration of DNA: 28.3 ng/uL
The ratio of DNA concentration to protein concentration(260/280): 1.66
The ratio of protein concentration to RNA concentration(260/230): 1.13

Team Newcastle iGEM 2009 31-07-09 no 2.JPG

Results for BBa_R0077
The concentration of DNA: 53.8 ng/uL
The ratio of DNA concentration to protein concentration(260/280): 1.75
The ratio of protein concentration to RNA concentration(260/230): 1.39

Team Newcastle iGEM 2009 31-07-09 no 3.JPG

2) BBa_C0077 and BBa_C0076 Transformants

Team Newcastle 2009 iGEM 31-07-09 IMG 0225.JPG


At last, colonies were found on the plates which contained DH5-alpha transformed with BBa_C0077 and BBa_c0076! The 2 LB-alone plates for both BBa_C0077 and BBa_C0076 transformants was completely covered in a lawn of bacteria. The LB + kan plate with the DH5-alpha cells transformed with BBa_C0077 yielded about 5 colonies whereas the LB + kan plate with the BBa_C0076 transformants yielded 100+ colonies.

However the plates will be stored in the fridge, over the weekend, for LB inoculations and future mini-preps to take place later (hopefully in Monday's lab session).

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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