Team:Newcastle/Labwork/21 September 2009

From 2009.igem.org

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(Practical Outline)
(Quantification of cotC and pMUTIN4)
 
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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 - 21st September 2009=
=Formal Lab Session - 21st September 2009=
-
==<u>Stochastic switch team</u>==
+
[[Image:Team Newcastle 2009 iGEM 21-09-09 IMG 1276.JPG|350px|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 21-09-09 IMG 1281.JPG|200px|right]]
Today we digested the sac minipreps with EcoRI and XbaI. It seems clear that there was something wrong with the minipreps (such as poor procedure) as there seemed to be little or no DNA in the sample.  
Today we digested the sac minipreps with EcoRI and XbaI. It seems clear that there was something wrong with the minipreps (such as poor procedure) as there seemed to be little or no DNA in the sample.  
Line 23: Line 35:
This was left in the fridge overnight to improve the ligation conditions.
This was left in the fridge overnight to improve the ligation conditions.
<br>
<br>
-
==<u>Metal Sensing Team</u>==
+
 
 +
==<u>Metal Sensor Team</u>==
===Introduction===
===Introduction===
===Practical Outline===
===Practical Outline===
 +
[[Image:Team Newcastle 2009 iGEM 21-09-09 IMG 1273.JPG|350px|center]]
Here are the list of tasks which need to be accomplished by the end of the day:
Here are the list of tasks which need to be accomplished by the end of the day:
<br>
<br>
-
# Run analysis digests of the 5 midi-preps of ''cotC'', ''kinA'', ''pGFP-rrnB'', ''pMUTIN4'' and ''pSB1AT3'' (midi-prepped in the [https://2009.igem.org/Team:Newcastle/Labwork/11_September_2009#Midi-prep_cotC-GFP-smtA.2C_kinA.2C_pGFP-rrnB.2C_pMUTIN4_and_pSB1AT3 11/09/09 lab session] and digested in the [https://2009.igem.org/Team:Newcastle/Labwork/18_September_2009#Analysing_cotC.2C_kinA.2C_pGFP-rrnB.2C_pMUTIN4_and_pSB1AT3_midi-preps 18/09/09 lab session])
+
* Run analysis digests of the 5 midi-preps of ''cotC'', ''kinA'', ''pGFP-rrnB'', ''pMUTIN4'' and ''pSB1AT3'' (midi-prepped in the [https://2009.igem.org/Team:Newcastle/Labwork/11_September_2009#Midi-prep_cotC-GFP-smtA.2C_kinA.2C_pGFP-rrnB.2C_pMUTIN4_and_pSB1AT3 11/09/09 lab session] and digested in the [https://2009.igem.org/Team:Newcastle/Labwork/18_September_2009#Analysing_cotC.2C_kinA.2C_pGFP-rrnB.2C_pMUTIN4_and_pSB1AT3_midi-preps 18/09/09 lab session])
 +
[[Image:Team Newcastle 2009 iGEM 21-09-09 IMG 1295.JPG|200px|right]]
 +
** If successful, double digest 40ul of ''pMUTIN4'' with ''BamHI'' and ''HindIII'' and place under DNA gel electrophoresis; excise band produced and extract DNA
 +
** If unsuccessful, inoculate 5ml of LB with ''E. coli'' containing ''pMUTIN4'' (for mini-preps and midi-preps)
 +
* Check PCR reaction (amplification of ''cotC-GFP-smtA'') on gel and clean up if successful
 +
** If successful, digest with ''BamHI'' and ''HindIII''
 +
* Should the ''pMUTIN4'' DNA extraction be a success and the ''cotC-GFP-smtA'' BioBrick be successfully amplified (by PCR) and extracted, ligate the two fragments together.
 +
** Reactions include:
 +
*** vector + insert + ligase
 +
*** vector + ligase
 +
*** vector and NO ligase
 +
* Inoculate 3ml of LB with TPA2 cells (for production of competent ''DH5-alpha E. coli'' cells)
 +
<br>
===Procedure===
===Procedure===
-
<center>
+
====Analysing midi-prep digests====
-
{|cellpadding="10"
+
[[Image:Team Newcastle 2009 iGEM Geldoc 2009-09-21 13hr 11min.jpg|400px|center]]
-
|{{#calendar: title=Team:Newcastle/Labwork |year=2009 | month=07 }}
+
<br>
-
|{{#calendar: title=Team:Newcastle/Labwork |year=2009 | month=08 }}
+
* Lane 1 = blank
-
|{{#calendar: title=Team:Newcastle/Labwork |year=2009 | month=09 }}
+
* Lane 2 = DNA HindIII ladder
 +
* Lane 3 = ''cotC'' midi-prep digest
 +
* Lane 4 = ''kinA'' midi-prep digest
 +
* Lane 5 = ''pGFP-rrnB'' midi-prep digest
 +
* Lane 6 = ''pMUTIN4'' midi-prep digest
 +
* Lane 7 = ''pSB1AT3'' midi-prep digest.
 +
* Lane 8 = PCR reaction 1
 +
* Lane 9 = PCR reaction 2
 +
* Lane 10 = blank
 +
* Lane 11 = ''pMUTIN4'' double digest (10ul)
 +
* Lane 12 = DNA HindIII ladder
 +
<br>
 +
 
 +
====Double digesting ''pMUTIN4'' midi-prep DNA====
 +
Double digest of 10ul of ''pMUTIN4'' DNA was conducted in the following manner:
 +
<br>
 +
* 10ul of ''pMUTIN4'' DNA
 +
* 1ul of FastDigest ''BamHI''
 +
* 1ul of FastDigest ''HindIII''
 +
* 2ul of restriction buffer
 +
* 6ul of sterile distilled water
 +
<br>
 +
The digests were allowed to commence for 1 hour under 37C incubation. Samples of this digest were then analysed through DNA gel electrophoresis and can be seen in the GelDoc photograph above.
 +
<br>
 +
 
 +
====Cleaning up ''cotC'' PCR product====
 +
The ''cotC_GFP_smtA'' BioBrick was cleaned up using GenElute's PCR clean-up kit and it's protocol was adhered to.
 +
 
 +
====Excising digested ''pMUTIN4'' from gel====
 +
Firstly 40ul of ''pMUTIN4'' was digested using ''BamHI'' and ''HindIII'' in the following manner:
 +
<br>
 +
* 40ul of ''pMUTIN4'' DNA
 +
* 4ul of FastDigest''BamHI''
 +
* 4ul of FastDigest''HindIII''
 +
* 8ul of buffer
 +
* 24ul of sterile distilled water
 +
<br>
 +
Incubated for 1 hour under 37C in waterbath. DNA was then all placed into agarose gel and DNA gel electrophoresis was allowed to commence for 20 minutes under 70 volts. Band was excised and cleaned up
 +
<br>
 +
Band weighed 0.351 grams so the amount of gel solubilization solution used was 1053ul.
 +
<br>
 +
 
 +
====Quantification of ''cotC'' and ''pMUTIN4''====
 +
''cotC'' = 26.6ng/ul
 +
''pMUTIN4'' = 23.6ng/ul
 +
<br>
 +
 
 +
==<u>Sporulation Tuning/Chassis Team</u>==
 +
[[Image:Team Newcastle 2009 iGEM 21-09-09 IMG 1275.JPG|200px|right]]
 +
===Introduction===
 +
* We have already got the double clone,the next thing need to do is to ligate this sleB:cwlJ fragment with pMutin4 plasmid to get the pspac sequence from pMutin4. pMutin4 contains HindIII and BamHI restriction sites, but our double clone sequence didn't contain those sites. If we want to ligate double clone fragment with pMutin4 backbone, we need PCR our double clone fragment and add HindIII and BamHI restriction sites.We designed cwlJsleB primers here.
 +
* We digest pMutin4 with HindIII and BamHI to get our plasmid backbone.
 +
* Midi Prep L1 and L2 transformation strains to get large amount of plasmid.
 +
* Our kinA synthesized part was arrived, we need to construct this gene into our integrate plasmid and transform it into B.subtilis.
 +
<br>
 +
 
 +
===Experiment procedure===
 +
 
 +
==== PCR doulbe clone fragment ====
 +
 
 +
* Prepare buffer mix and Taq
 +
 
 +
  Reaction buffer  10ul x 4 = 40ul
 +
            dNTP  2ul x 4 =  8ul
 +
  --------------------------------
 +
                              48ul
 +
  12ul for each reaction
 +
<br>
 +
  GoTaq(5U/ul)  0.25ul x 2 = 0.5ul
 +
  ddH2O                        4.5ul
 +
  ----------------------------------
 +
                                5ul
 +
  2.5ul for each reaction
 +
 
 +
 
 +
{| border="1"
 +
|+ Exp. PCR experiment for gene cwlJ:sleB
 +
! No. !! Water (ul) !! PCR Mix (ul) !! Forward Primer (ul) !! Reverse Primer (ul) !! Template (ul) !! Polymerase used (ul) !! Total Volume (ul)
 +
|-
 +
| 1 || 28.5 || 12 || cwlJsleBForward 2.5ul || cwlJsleBReverse 2.5ul  || pSB1AT3:cwlJ:sleB 2ul || GoTaq 2.5ul || 50
 +
|-
 +
| 2 || 30.5 || 12 || cwlJsleBForward 2.5ul || cwlJsleBReverse 2.5ul  || 0ul || GoTaq 2.5ul|| 50
 +
|-
|}
|}
-
</center>
+
<br>
 +
* PCR procedure: STD50
 +
<br>
 +
95C 2min -->[95C 30S --> 50C 30S --> 75C 1min] 30 runs --> 75C 5min --> store at 4C
 +
 
 +
==== Prepare for Midi Prep ====
 +
* Add 50ml LB+Amp+Tet liquid medium into a flask, get 200ul cell mixture from Mini prep culture.
 +
* Culture L1 and L2 overnight.
 +
 
 +
==== Digest pMutin4 plasmid for ligation ====
 +
* Prepare the digest reaction.
 +
  dd H2O                    7ul
 +
  10X fast digest buffer    7ul
 +
  Fast HindIII              3ul
 +
  Fast BamHI                3ul
 +
  pMutin4 plasmid          50ul
 +
  ------------------------------
 +
                            70ul
 +
* Incubate 1 hour at 37 degree.
 +
 
 +
==== Digest kinA fragment ====
 +
[[Image:Team Newcastle 2009 iGEM 21-09-09 IMG 1282.JPG|200px|right]]
 +
* Digest pMK-RQ vector to get kinA fragment.(Jess has done this part)
 +
* Run big well gel to seperate kinA and pMK-RQ backbone.
 +
* Use gel extraction kit to purify kinA fragment.
 +
 
 +
<br>
 +
 
 +
===Conclusion===
 +
 
 +
* When we cut pMK-RQ with EcoRI and NheI, both pMK-RQ back bone and kinA fragment are about 2k bp. To get the purified kinA fragment, we need to run the gel for a longer time to seperate the two bands. The other way is to introduce the third enzyme which can cut the backbone into 2 pieces and keep kinA's integrability.
 +
 
 +
===Futher plan===
 +
* Ligate kinA with pGFP-rrnB.
 +
* Ligate cwlJ:sleB fragment with pMutin4 and transform ligated plasmid into E.coli.
 +
{{:Team:Newcastle/Project/Labwork/CalTemplate}}
{{:Team:Newcastle/Footer}}
{{:Team:Newcastle/Footer}}
{{:Team:Newcastle/Right}}
{{:Team:Newcastle/Right}}

Latest revision as of 03:30, 22 October 2009


Team Newcastle 2009 iGEM ProbationaryP-Sign.PNG

Formal Lab Session - 21st September 2009

Team Newcastle 2009 iGEM 21-09-09 IMG 1276.JPG


Overview





Stochastic Switch Team

Team Newcastle 2009 iGEM 21-09-09 IMG 1281.JPG

Today we digested the sac minipreps with EcoRI and XbaI. It seems clear that there was something wrong with the minipreps (such as poor procedure) as there seemed to be little or no DNA in the sample.

Did a gel fragment clean up on the sspb fragment cut from the gel, this was put in the 'fragments' box in the freezer ready for later.

50ul of ara+pSB1AT3 plasmid was cut with SpeI and PstI in order to insert the sspb fragment after the operator. Rather than doing a gel fragment prep a PCR clean up (kit) was done on the digest to save time.

We ligated the ara + sspb fragments using Chris' method:

  • 2ul Ligase buffer
  • 2.5ul Vector DNA
  • 14.5ul insert DNA
  • 1ul ligase

= 20ul

This was left in the fridge overnight to improve the ligation conditions.

Metal Sensor Team

Introduction

Practical Outline

Team Newcastle 2009 iGEM 21-09-09 IMG 1273.JPG

Here are the list of tasks which need to be accomplished by the end of the day:

Team Newcastle 2009 iGEM 21-09-09 IMG 1295.JPG
    • If successful, double digest 40ul of pMUTIN4 with BamHI and HindIII and place under DNA gel electrophoresis; excise band produced and extract DNA
    • If unsuccessful, inoculate 5ml of LB with E. coli containing pMUTIN4 (for mini-preps and midi-preps)
  • Check PCR reaction (amplification of cotC-GFP-smtA) on gel and clean up if successful
    • If successful, digest with BamHI and HindIII
  • Should the pMUTIN4 DNA extraction be a success and the cotC-GFP-smtA BioBrick be successfully amplified (by PCR) and extracted, ligate the two fragments together.
    • Reactions include:
      • vector + insert + ligase
      • vector + ligase
      • vector and NO ligase
  • Inoculate 3ml of LB with TPA2 cells (for production of competent DH5-alpha E. coli cells)


Procedure

Analysing midi-prep digests

Team Newcastle 2009 iGEM Geldoc 2009-09-21 13hr 11min.jpg


  • Lane 1 = blank
  • Lane 2 = DNA HindIII ladder
  • Lane 3 = cotC midi-prep digest
  • Lane 4 = kinA midi-prep digest
  • Lane 5 = pGFP-rrnB midi-prep digest
  • Lane 6 = pMUTIN4 midi-prep digest
  • Lane 7 = pSB1AT3 midi-prep digest.
  • Lane 8 = PCR reaction 1
  • Lane 9 = PCR reaction 2
  • Lane 10 = blank
  • Lane 11 = pMUTIN4 double digest (10ul)
  • Lane 12 = DNA HindIII ladder


Double digesting pMUTIN4 midi-prep DNA

Double digest of 10ul of pMUTIN4 DNA was conducted in the following manner:

  • 10ul of pMUTIN4 DNA
  • 1ul of FastDigest BamHI
  • 1ul of FastDigest HindIII
  • 2ul of restriction buffer
  • 6ul of sterile distilled water


The digests were allowed to commence for 1 hour under 37C incubation. Samples of this digest were then analysed through DNA gel electrophoresis and can be seen in the GelDoc photograph above.

Cleaning up cotC PCR product

The cotC_GFP_smtA BioBrick was cleaned up using GenElute's PCR clean-up kit and it's protocol was adhered to.

Excising digested pMUTIN4 from gel

Firstly 40ul of pMUTIN4 was digested using BamHI and HindIII in the following manner:

  • 40ul of pMUTIN4 DNA
  • 4ul of FastDigestBamHI
  • 4ul of FastDigestHindIII
  • 8ul of buffer
  • 24ul of sterile distilled water


Incubated for 1 hour under 37C in waterbath. DNA was then all placed into agarose gel and DNA gel electrophoresis was allowed to commence for 20 minutes under 70 volts. Band was excised and cleaned up
Band weighed 0.351 grams so the amount of gel solubilization solution used was 1053ul.

Quantification of cotC and pMUTIN4

cotC = 26.6ng/ul pMUTIN4 = 23.6ng/ul

Sporulation Tuning/Chassis Team

Team Newcastle 2009 iGEM 21-09-09 IMG 1275.JPG

Introduction

  • We have already got the double clone,the next thing need to do is to ligate this sleB:cwlJ fragment with pMutin4 plasmid to get the pspac sequence from pMutin4. pMutin4 contains HindIII and BamHI restriction sites, but our double clone sequence didn't contain those sites. If we want to ligate double clone fragment with pMutin4 backbone, we need PCR our double clone fragment and add HindIII and BamHI restriction sites.We designed cwlJsleB primers here.
  • We digest pMutin4 with HindIII and BamHI to get our plasmid backbone.
  • Midi Prep L1 and L2 transformation strains to get large amount of plasmid.
  • Our kinA synthesized part was arrived, we need to construct this gene into our integrate plasmid and transform it into B.subtilis.


Experiment procedure

PCR doulbe clone fragment

  • Prepare buffer mix and Taq
 Reaction buffer  10ul x 4 = 40ul
            dNTP   2ul x 4 =  8ul
 --------------------------------
                             48ul
 12ul for each reaction


 GoTaq(5U/ul)   0.25ul x 2 =  0.5ul
 ddH2O                        4.5ul
 ----------------------------------
                                5ul
 2.5ul for each reaction


Exp. PCR experiment for gene cwlJ:sleB
No. Water (ul) PCR Mix (ul) Forward Primer (ul) Reverse Primer (ul) Template (ul) Polymerase used (ul) Total Volume (ul)
1 28.5 12 cwlJsleBForward 2.5ul cwlJsleBReverse 2.5ul pSB1AT3:cwlJ:sleB 2ul GoTaq 2.5ul 50
2 30.5 12 cwlJsleBForward 2.5ul cwlJsleBReverse 2.5ul 0ul GoTaq 2.5ul 50


  • PCR procedure: STD50


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

Prepare for Midi Prep

  • Add 50ml LB+Amp+Tet liquid medium into a flask, get 200ul cell mixture from Mini prep culture.
  • Culture L1 and L2 overnight.

Digest pMutin4 plasmid for ligation

  • Prepare the digest reaction.
 dd H2O                     7ul
 10X fast digest buffer     7ul
 Fast HindIII               3ul
 Fast BamHI                 3ul
 pMutin4 plasmid           50ul
 ------------------------------
                           70ul
  • Incubate 1 hour at 37 degree.

Digest kinA fragment

Team Newcastle 2009 iGEM 21-09-09 IMG 1282.JPG
  • Digest pMK-RQ vector to get kinA fragment.(Jess has done this part)
  • Run big well gel to seperate kinA and pMK-RQ backbone.
  • Use gel extraction kit to purify kinA fragment.


Conclusion

  • When we cut pMK-RQ with EcoRI and NheI, both pMK-RQ back bone and kinA fragment are about 2k bp. To get the purified kinA fragment, we need to run the gel for a longer time to seperate the two bands. The other way is to introduce the third enzyme which can cut the backbone into 2 pieces and keep kinA's integrability.

Futher plan

  • Ligate kinA with pGFP-rrnB.
  • Ligate cwlJ:sleB fragment with pMutin4 and transform ligated plasmid into E.coli.
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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