Difference between revisions of "IGEM 2010 Project"

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http://gcat.davidson.edu/iGem10/index.html
 
http://gcat.davidson.edu/iGem10/index.html
 +
 +
'''Paris IGEM 2007 Results'''
 +
{| class="wikitable" style="text-align:center" border="1" cellpadding="2"
 +
|'''T'''
 +
|'''r'''
 +
|-
 +
 +
|19.5 ||40.16
 +
|-
 +
 +
|20.5 ||39.61
 +
|-
 +
 +
|25.5 ||36.76
 +
|-
 +
 +
|30.5 ||33.78
 +
|-
 +
 +
|35.5 ||30.66
 +
|-
 +
 +
|40.5 ||27.39
 +
|-
 +
 +
|45.5 ||23.97
 +
|-
 +
 +
|50.5 ||20.39
 +
|-
 +
 +
|55.5 ||16.64
 +
|-
 +
 +
|}
 +
 +
 +
This is a chart of the experimental group in the Paris IGEM 2007 project. I used the formula r=1-10^(.004*T)/2 where r is the recombination rate (how many times Cre makes a cut and a Scar site is formed) and T is the generation time in minutes (How long it takes the cell to divide).
 +
 +
'''Paris IGEM 2007 Results'''
 +
{| class="wikitable" style="text-align:center" border="1" cellpadding="2"
 +
|'''r'''
 +
|'''G'''
 +
|-
 +
 +
|.05 ||103.3
 +
|-
 +
 +
|.10 ||50.3
 +
|-
 +
 +
|.15 ||32.6
 +
|-
 +
 +
|.20 ||23.7
 +
|-
 +
 +
|.25 ||18.4
 +
|-
 +
 +
|.30 ||14.9
 +
|-
 +
 +
|.35 ||12.3
 +
|-
 +
 +
|.40 ||10.4
 +
|-
 +
 +
|.45 ||8.9
 +
|-
 +
 +
|.50 ||7.6
 +
|-
 +
 +
|.55 ||6.6
 +
|-
 +
 +
|.60 ||5.8
 +
|-
 +
 +
|.65 ||5.0
 +
|-
 +
 +
|.70 ||4.4
 +
|-
 +
 +
|.75 ||3.8
 +
|-
 +
 +
|.80 ||3.3
 +
|-
 +
 +
|.85 ||2.8
 +
|-
 +
 +
|.90 ||2.3
 +
|-
 +
 +
|.95 ||1.8
 +
|-
 +
 +
|}
 +
 +
This is a chart of the experimental group in the Paris IGEM 2007 project. I used the formula G=log(1/200)/log(1-r) where r is the recombination rate (how many times Cre makes a cut and a Scar site is formed) and G is the number of generations (or the number of times the cell will need to divide). I am making an assumption here that the initial prey population (the plasmids in the cell) is 200.
  
 
== Biology Sub-Projects==
 
== Biology Sub-Projects==
Line 174: Line 279:
 
This chart shows flourescene levels of different promoter constructs with varying levels of IPTG added (error bars with standard error can be seen on the graph).  Note:  This experiment is still in progress.  More data will be posted when available.   
 
This chart shows flourescene levels of different promoter constructs with varying levels of IPTG added (error bars with standard error can be seen on the graph).  Note:  This experiment is still in progress.  More data will be posted when available.   
  
−
width="30"[[Image:wiki4.jpg]]
+
[[Image:wiki4.jpg]]
 +
 
  
 
'''Tet-trations'''<br>
 
'''Tet-trations'''<br>
  
  
−
 
+
[[Image:cell turbidity.jpg]]
  
  
Line 198: Line 304:
 
|-  
 
|-  
  
−
|<span style="color:#B22222"> '''loxm2 Forward in pSB1A2''' </span>  || <span style="color:#B22222"> I ligated loxm2 F with the plasmid and have prepared the DNA for sequencing to confirm what is there.  ||  [http://partsregistry.org/Part:BBa_K315004] </span> <br> <span style="color:#B22222"> ''loxm2'' does not exist in the registry.  We ordered oligos and constructed the site in the lab. </span> || Tom
+
|<span style="color:#006400"> '''loxm2 Forward in pSB1A2''' </span>  || <span style="color:#B22222"> I ligated loxm2 F with the plasmid and have prepared the DNA for sequencing to confirm what is there.  ||  [http://partsregistry.org/Part:BBa_K315004] </span> <br> <span style="color:#B22222"> ''loxm2'' does not exist in the registry.  We ordered oligos and constructed the site in the lab. </span> || Tom
 +
|-
 +
 
 +
|<span style="color:#006400"> '''loxm2 Reverse in pSB1A2''' </span>  || <span style="color:#B22222"> I ligated loxm2 F with the plasmid and have prepared the DNA for sequencing to confirm what is there.  ||  [http://partsregistry.org/Part:BBa_K315005] </span> <br> <span style="color:#B22222">  ''loxm2'' does not exist in the registry.  We ordered oligos and constructed the site in the lab. </span> || Tom
 
|-  
 
|-  
  
−
|<span style="color:#B22222"> '''loxm2 Reverse in pSB1A2''' </span>  || <span style="color:#B22222"> I ligated loxm2 F with the plasmid and have prepared the DNA for sequencing to confirm what is there.  ||  [http://partsregistry.org/Part:BBa_K315005] </span> <br> <span style="color:#B22222"> ''loxm2'' does not exist in the registry. We ordered oligos and constructed the site in the lab. </span> || Tom
+
|<span style="color:#B22222"> '''loxBri forward in pSB1A2''' </span>  || <span style="color:#B22222"> 4 colonies grew with the correct sized insert from colony PCR verification and will be sent off for sequencing.  ||  [http://partsregistry.org/Part:pSB1A2 pSB1A2] </span> <br> <span style="color:#B22222"> loxBri does not exist in the registry. We ordered this oligos with 3 mutations and transformed in lab. </span> || Bri
 
|-  
 
|-  
  
−
|<span style="color:#B22222"> '''Insert Info Here''' </span>  || <span style="color:#B22222"> what is built so far? ||  [http://partsregistry.org/Part:BBa_K199000 change to correct link] </span> <br> <span style="color:#B22222"> describe intermediate </span> || your name here
+
|<span style="color:#B22222"> '''loxBri reverse in pSB1A2''' </span>  || <span style="color:#B22222"> I had 3 successful colonies from this oligos ligation that were also confirmed by colony PCR that will be sent off for sequencing. ||  [http://partsregistry.org/Part:pSB1A2 pSB1A2] </span> <br> <span style="color:#B22222"> loxBri does not exist in the registry. This oligos was also transformed in the lab. </span> || Bri
 
|-  
 
|-  
  
−
|<span style="color:#B22222"> '''Insert Info Here''' </span>  || <span style="color:#B22222"> what is built so far? ||  [http://partsregistry.org/Part:BBa_K199000 change to correct link] </span> <br> <span style="color:#B22222"> describe intermediate </span> || your name here
+
|<span style="color:#B22222"> '''loxP reverse in pSB1A2''' </span>  || <span style="color:#B22222"> I had 5 successful colonies from this oligos ligation that were also confirmed by colony PCR. They will be sent off for sequencing. ||  [http://partsregistry.org/Part:BBa_K206013 loxP reverse] </span> <br> <span style="color:#B22222"> loxP reverse exists in the registry. We ordered this oligos and ligated it into pSB1A2 in the lab. </span> || Bri
 
|-  
 
|-  
  
−
|<span style="color:#B22222"> '''Insert Info Here''' </span>  || <span style="color:#B22222"> what is built so far? ||  [http://partsregistry.org/Part:BBa_K199000 change to correct link] </span> <br> <span style="color:#B22222"> describe intermediate </span> || your name here
+
|<span style="color:#B22222"> '''loxN Forward in pSB1A2''' </span>  || <span style="color:#B22222"> I had 5 successful colonies from this oligos ligation that were also confirmed by colony PCR. They are sent off for sequencing and four of them were confirmed to be correct. ||  [http://partsregistry.org/Part:BBa_K315007] </span> <br> <span style="color:#B22222"> loxN forward does not exist in the registry. We ordered the oligos and built it in the lab.  </span> || Anvi
 
|-  
 
|-  
  
−
|<span style="color:#B22222"> '''Insert Info Here''' </span>  || <span style="color:#B22222"> what is built so far? ||  [http://partsregistry.org/Part:BBa_K199000 change to correct link] </span> <br> <span style="color:#B22222"> describe intermediate </span> || your name here
+
 
 +
|<span style="color:#B22222"> '''loxN Reverse in pSB1A2''' </span>  || <span style="color:#B22222"> I had 3 successful colonies from this oligos ligation that were also confirmed by colony PCR. They are sent off for sequencing and two of them were confirmed to be correct.  ||  [http://partsregistry.org/Part:BBa_K315011] </span> <br> <span style="color:#B22222"> loxN reverse does not exist in the registry. We ordered the oligos and built it in the lab.  </span> || Anvi
 +
|-
 +
|<span style="color:#006400"> '''lox2272 Reverse in pSB1A2</span>  || <span style="color:#006400"> I had 1 successful colony from this oligos ligation that were also confirmed by sequencing and its cells have been plate on LB Amp plates and frozen into freezer stocks. ||  [http://partsregistry.org/Part:BBa_K315010] </span> <br> <span style="color:#006400"> lox2272 reverse does not exist in the registry. We ordered the oligos and built it in the lab.  </span> || Jamela
 
|-  
 
|-  
 +
|<span style="color:#006400"> '''lox2272 Forward in pSB1A2</span>  || <span style="color:#006400"> I had 3 successful colony from this oligos ligation that were also confirmed by sequencing and its cells have been plate on LB Amp plates and frozen into freezer stocks.  ||  [http://partsregistry.org/Part:BBa_K315013] </span> <br> <span style="color:#006400"> lox2272 foward does not exist in the registry. We ordered the oligos and built it in the lab.  </span> || Jamela
 +
 +
 
|}
 
|}
 
<br>
 
<br>
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|-  
 
|-  
  
−
|<span style="color:#B22222"> '''Insert Info Here''' </span>  || <span style="color:#B22222"> what is built so far?  ||  [http://partsregistry.org/Part:BBa_K199000 change to correct link] </span> <br> <span style="color:#B22222"> describe intermediate </span> || your name here
+
|<span style="color:#B22222"> '''I718008 (pBAD+RBS+cre) in pSB3K3''' </span>  || <span style="color:#B22222"> At this point, I have ligated and transformed the cells but I am having trouble growing it in the LB + kan media. ||  [http://partsregistry.org/Part:BBa_I718008 I718008][http://partsregistry.org/wiki/index.php?title=Part:pSB3K5] </span> <br> <span style="color:#B22222"> describe intermediate </span> || Anvi
 
|-  
 
|-  
  
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Data showing the varying levels of expression between pSBIA7 and pSBIA2
 
Data showing the varying levels of expression between pSBIA7 and pSBIA2
  
−
[[Image:curtiss1.jpg]]
+
[[Image:curtiss3.jpg]]

Latest revision as of 19:41, 7 July 2010


We need to start capturing what we are doing, and why.

Please use this page as a starting place.

We need an overall description of our project at the overview level as well as the subsections and phases of implementation.

Math Sub-Projects

Counting Permutations


Improving Oligo Assembler We adapted the lancelator (http://gcat.davidson.edu/IGEM06/oligo.html), a program created by Lance Harden as a part of the 2006 iGem team, so that it would execute faster and can handle longer sequences. The old program could only handle sequences of 300 bp or shorter. Also, the more oligos the program broke the sequence into, the longer it took to run, and for 8 or more the run time was simply unreasonable. However, for the sequences it could handle it always finds the optimal oligos to use. Our program allows the user to enter a sequence of any length, and the length does not significantly effect runtime. In addition, we added extra features such as checking for and removing BioBrick restriction sites and adding BioBrick primers. While our program does not always find the optimal oligos, it still does very well which is an acceptable compromise because the runtime is improved so dramatically.

http://gcat.davidson.edu/iGem10/index.html

Paris IGEM 2007 Results

T r
19.5 40.16
20.5 39.61
25.5 36.76
30.5 33.78
35.5 30.66
40.5 27.39
45.5 23.97
50.5 20.39
55.5 16.64


This is a chart of the experimental group in the Paris IGEM 2007 project. I used the formula r=1-10^(.004*T)/2 where r is the recombination rate (how many times Cre makes a cut and a Scar site is formed) and T is the generation time in minutes (How long it takes the cell to divide).

Paris IGEM 2007 Results

r G
.05 103.3
.10 50.3
.15 32.6
.20 23.7
.25 18.4
.30 14.9
.35 12.3
.40 10.4
.45 8.9
.50 7.6
.55 6.6
.60 5.8
.65 5.0
.70 4.4
.75 3.8
.80 3.3
.85 2.8
.90 2.3
.95 1.8

This is a chart of the experimental group in the Paris IGEM 2007 project. I used the formula G=log(1/200)/log(1-r) where r is the recombination rate (how many times Cre makes a cut and a Scar site is formed) and G is the number of generations (or the number of times the cell will need to divide). I am making an assumption here that the initial prey population (the plasmids in the cell) is 200.

Biology Sub-Projects

Codon Optimization


Segment Number of Base Pairs Wild Type Sequence Optimized Sequence Deoptimized Sequence
1 141 Atgaaatctaacaatgcgctcatcgtcatcctcggcaccgtcaccctggatgctgtaggcataggcttggttatgccggtactgccgggcctcttgcgggatatcgtccattccgacagcatcgccagtcactatggcgtg ATGAAATCTAACAACGCGCTGATCGTTATCCTGGGTACCGTTACCCTGGACGCGGTTGGTATCGGTCTGGTTATGCCGGTTCTGCCGGGTCTGCTGCGTGACATCGTTCACTCTGACTCTATCGCGTCTCACTACGGTGTT ATGAAGAGTAATAATGCCCTAATAGTCATACTAGGAACAGTCACACTAGATGCCGTCGGAATAGGACTCGTCATGCCCGTCCTACCCGGACTACTAAGGGATATAGTCCATAGTGATAGTATAGCCAGTCATTATGGAGTC
2 138 ctatatgcgttgatgcaatttctatgcgcacccgttctcggagcactgtccgaccgctttggccgccgcccagtcctgctcgcttcgctacttggagccactatcgactacgcgatcatggcgaccacacccgtcctg CTGTACGCGCTGATGCAGTTCCTGTGCGCGCCGGTTCTGGGTGCGCTGTCTGACCGTTTCGGTCGTCGTCCGGTTCTGCTGGCGTCTCTGCTGGGTGCGACCATCGACTACGCGATCATGGCGACCACCCCGGTTCTG CTATATGCCCTAATGCAATTTCTATGTGCCCCCGTCCTAGGAGCCCTAAGTGATAGGTTTGGAAGGAGGCCCGTCCTACTAGCCAGTCTACTAGGAGCCACAATAGATTATGCCATAATGGCCACAACACCCGTCCTA
3 177 tacgccggacgcatcgtggccggcatcaccggcgccacaggtgcggttgctggcgcctatatcgccgacatcaccgatggggaagatcgggctcgccacttcgggctcatgagcgcttgtttcggcgtgggtatggtggcaggccccgtggccgggggactgttgggcgccatctcc TACGCGGGTCGTATCGTTGCGGGTATCACCGGTGCGACCGGTGCGGTTGCGGGTGCGTACATCGCGGACATCACCGACGGTGAAGACCGTGCGCGTCACTTCGGTCTGATGTCTGCGTGCTTCGGTGTTGGTATGGTTGCGGGTCCGGTTGCGGGTGGTCTGCTGGGTGCGATCTCT TATGCCGGAAGGATAGTCGCCGGAATAACAGGAGCCACAGGAGCCGTCGCCGGAGCCTATATAGCCGATATAACAGATGGAGAGGATAGGGCCAGGCATTTTGGACTAATGAGTGCCTGTTTTGGAGTCGGAATGGTCGCCGGACCCGTCGCCGGAGGACTACTAGGAGCCATAAGT
4 81 ccattccttgcggcggcggtgctcaacggcctcaacctactactgggctgcttcctaatgcaggagtcgcataagggagag CCGTTCCTGGCGGCGGCGGTTCTGAACGGTCTGAACCTGCTGCTGGGTTGCTTCCTGATGCAGGAATCTCACAAAGGTGAA CCCTTTCTAGCCGCCGCCGTCCTAAATGGACTAAATCTACTACTAGGATGTTTTCTAATGCAAGAGAGTCATAAGGGAGAG

Note: All above segments have been optimized and deoptimized using the online Optimizer program.

To create the optimized and deoptimized segments of the Tet A gene we used the sequence that the Optimizer program gave us and put it into the Lancelator a program created by Lance Harden as part of the 2006 iGEM team. After getting the recommended Oligo sequences from the Lancelator, we added necessary "sticky ends" that were compatible with the naturally occurring restriction enzyme sites that we discovered (see Restriction Enzymes below). At this time we have ordered Oligo parts for segments 1 and 2 of the Tet A gene. The Oligos that were ordered can be seen below.


Segment 1 Oligos


Optimized

top 1 5' AATTCGCGGCCGCTTCTAGATGAAATCTAACAACGCGCTGATCGTTATCCTGGGTACCG 3’

top 2 5' TTACCCTGGACGCGGTTGGTATCGGTCTGGTTATGCCGGTTCTGCCGGGTCTGCTGCGTGAC 3’

top 3 5' ATCGTTCACTCTGACTCTATCGCGTCTCACTACGGTGTTCTG 3’

bottom 2 5' CATAACCAGACCGATACCAACCGCGTCCAGGGTAACGGTAC CCAGGATAACGATCAGCGCGTTGTTAGATTTCATCTAGAAGCGGCCGCG 3’

bottom 1 5' CTAGCAGAACACCGTAGTGAGACGCGATAGAGTCAGAGTGAACGATGTCACGCAGCAGACCCGGCAGAACCGG 3’

Deoptimized

top 1 5' AATTCGCGGCCGCTTCTAGATGAAGAGTAATAATGCCCTAATAGTCATACTAGGAACAG 3’

top 2 5' TCACACTAGATGCCGTCGGAATAGGACTCGTCATGCCCGTCCTACCCGGACTACTAAGGGA 3’

top 3 5' TATAGTCCATAGTGATAGTATAGCCAGTCATTATGGAGTCCTG 3’

bottom 2 5' GAGTCCTATTCCGACGGCATCTAGTGTGACTGTTCCTAGTATG ACTATTAGGGCATTATTACTCTTCATCTAGAAGCGGCCGCG 3’

bottom 1 5' CTAGCAGGACTCCATAATGACTGGCTATACTATCACTATGGACTATATCCCTTAGTAGTCCGGGTAGGACGGGCATGAC 3’


Segment 2 Oligos


Optimized

top 1 5' CTAGCCTGTACGCGCTGATGCAGTTCCTGTGCGCGCCGGTTCTGGGTGCGCTGTCTGAC 3’

top 2 5' CGTTTCGGTCGTCGTCCGGTTCTGCTGGCGTCTCTGCTGGGTGCGACCATCGACTAC 3’

top 3 5' GCGATCATGGCGACCACCCCGGTTCTGTG 3’

bottom 1 5' GCGCACAGGAACTGCATCAGCGCGTACAGG 3’

bottom 2 5' CCAGCAGAACCGGACGACGACCGAAACGGTCAGACAGCGCACCCAGAACCGGC 3’

bottom 3 5' GATCCACAGAACCGGGGTGGTCGCCATGATCGCGTAGTCGATGGTCGCACCCAGCAGAGACG 3’

Deoptimized

top 1 5' CTAGCGCTATATGCCCTAATGCAATTTCTATGTGCCCCCGTCCTAGGAGCCCTAAGTG
3'

top 2 5' ATAGGTTTGGAAGGAGGCCCGTCCTACTAGCCAGTCTACTAGGAGCCACAATAGAT
3'

top 3 5' TATGCCATAATGGCCACAACACCCGTCCTATG
3'

bottom 1 5' GGCACATAGAAATTGCATTAGGGCATATAGCG 3'


bottom 2 5' TAGGACGGGCCTCCTTCCAAACCTATCACTTAGGGCTCCTAGGACGGG 3'


bottom 3 5' GATCCATAGGACGGGTGTTGTGGCCATTATGGCATAATCTATTGTGGCTCCTAGTAGACTGGCTAG 3'

Wiki3.jpg


Restriction Enzymes

To insert the annealed Oligo segments that were created we had to digest the Tet A gene using naturally occurring enzyme restriction sites that did not exist in the rest of the gene or in the plasmid (pSBIA2).


Segment First Restriction Enzyme Second Restriction Enzyme
1 EcoRI NheI
2 NheI BamHI
3 BamHI SphI
4 SphI SalI

Parts Used (to be used)

Part Registry Link Construct Including Part
Tet A (tetracycline resistance gene) J31007 Tet A (forward) promoter-RBS-RFP-RBS-TetA on pSBIA2
pLac-RBS-RFP I715039 pLac-RBS-RFP Possibly: pLac-RBS-RFP-RBS-TetA on pSBIA2
pLac-RBS-RFP-RBS-TetA-TT on pSBIAK3 S04435 pLac-RBS-RFP-RBS-TetA-TT Possibly: pLac-RBS-RFP-RBS-TetA-TT on pSBIA2
Part Name and Registry Number Registry Link Construct
Part Name and Registry Number Registry Link Construct


Promoters

This chart shows flourescene levels of different promoter constructs with varying levels of IPTG added (error bars with standard error can be seen on the graph). Note: This experiment is still in progress. More data will be posted when available.

Wiki4.jpg


Tet-trations


Cell turbidity.jpg


Making and Testing lox_ Sites

Green Part has been cloned and sequence verified; Red Part is under construction

Final Construct Current Status Registry Number and Link Primary Team Member
lox5171 Forward in pSB1A2 I got colonies on my second attempt. Once I isolate the plasmid, it will be sent off for sequencing. pSB1A2
lox5171 does not exist in the registry. We ordered oligos and constructed the site in the lab. 		Nitya
lox5171 Reverse in pSB1A2 This plasmid will also be sent off for sequencing soon. pSB1A2
lox5171 does not exist in the registry. We ordered oligos and constructed the site in the lab. 		Nitya
loxm2 Forward in pSB1A2 I ligated loxm2 F with the plasmid and have prepared the DNA for sequencing to confirm what is there. [1]
loxm2 does not exist in the registry. We ordered oligos and constructed the site in the lab. 		Tom
loxm2 Reverse in pSB1A2 I ligated loxm2 F with the plasmid and have prepared the DNA for sequencing to confirm what is there. [2]
loxm2 does not exist in the registry. We ordered oligos and constructed the site in the lab. 		Tom
loxBri forward in pSB1A2 4 colonies grew with the correct sized insert from colony PCR verification and will be sent off for sequencing. pSB1A2
loxBri does not exist in the registry. We ordered this oligos with 3 mutations and transformed in lab. 		Bri
loxBri reverse in pSB1A2 I had 3 successful colonies from this oligos ligation that were also confirmed by colony PCR that will be sent off for sequencing. pSB1A2
loxBri does not exist in the registry. This oligos was also transformed in the lab. 		Bri
loxP reverse in pSB1A2 I had 5 successful colonies from this oligos ligation that were also confirmed by colony PCR. They will be sent off for sequencing. loxP reverse
loxP reverse exists in the registry. We ordered this oligos and ligated it into pSB1A2 in the lab. 		Bri
loxN Forward in pSB1A2 I had 5 successful colonies from this oligos ligation that were also confirmed by colony PCR. They are sent off for sequencing and four of them were confirmed to be correct. [3]
loxN forward does not exist in the registry. We ordered the oligos and built it in the lab. 		Anvi
loxN Reverse in pSB1A2 I had 3 successful colonies from this oligos ligation that were also confirmed by colony PCR. They are sent off for sequencing and two of them were confirmed to be correct. [4]
loxN reverse does not exist in the registry. We ordered the oligos and built it in the lab. 		Anvi
lox2272 Reverse in pSB1A2 I had 1 successful colony from this oligos ligation that were also confirmed by sequencing and its cells have been plate on LB Amp plates and frozen into freezer stocks. [5]
lox2272 reverse does not exist in the registry. We ordered the oligos and built it in the lab. 		Jamela
lox2272 Forward in pSB1A2 I had 3 successful colony from this oligos ligation that were also confirmed by sequencing and its cells have been plate on LB Amp plates and frozen into freezer stocks. [6]
lox2272 foward does not exist in the registry. We ordered the oligos and built it in the lab. 		Jamela



Testing Cre Activity

Green Part has been cloned and sequence verified; Red Part is under construction

Final Construct Current Status Registry Number and Link Primary Team Member
I718008 (pBAD+RBS+cre) in pSB4K5 At this point, I have isolated both the insert and the plasmid, but my two attempts at ligation have not produced any colonies. I718008 pSB4K5
Nitya
I718008 (pBAD+RBS+cre) in pSB3K3 At this point, I have ligated and transformed the cells but I am having trouble growing it in the LB + kan media. I718008[7]
describe intermediate 		Anvi
Insert Info Here what is built so far? change to correct link
describe intermediate 		your name here
Insert Info Here what is built so far? change to correct link
describe intermediate 		your name here
Insert Info Here what is built so far? change to correct link
describe intermediate 		your name here
Insert Info Here what is built so far? change to correct link
describe intermediate 		your name here
Insert Info Here what is built so far? change to correct link
describe intermediate 		your name here
Insert Info Here what is built so far? change to correct link
describe intermediate 		your name here


pSBIA7 & pSBIA2

Data showing the varying levels of expression between pSBIA7 and pSBIA2

Curtiss3.jpg

Retrieved from "https://gcat.davidson.edu/GcatWiki/index.php?title=IGEM_2010_Project&oldid=11623"