Difference between revisions of "IGEM 2010 Project"

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(Biology Sub-Projects)
(Biology Sub-Projects)
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!width="30"|Primary Team Member
 
!width="30"|Primary Team Member
 
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|<span style="color:#B22222"> '''''lox5171'' Forward in pSB1A2''' </span>  || <span style="color:#B22222"> I got colonies on my second attempt.  Once I isolate the plasmid, it will be sent off for sequencing.  ||  [http://partsregistry.org/Part:pSB1A2] </span> <br> <span style="color:#B22222"> ''lox5171'' does not exist in the registry.  We ordered oligos and constructed the site in the lab. </span> || Nitya
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|<span style="color:#B22222"> '''''lox5171'' Forward in pSB1A2''' </span>  || <span style="color:#B22222"> I got colonies on my second attempt.  Once I isolate the plasmid, it will be sent off for sequencing.  ||  [http://partsregistry.org/Part:pSB1A2 pSB1A2] </span> <br> <span style="color:#B22222"> ''lox5171'' does not exist in the registry.  We ordered oligos and constructed the site in the lab. </span> || Nitya
 
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|<span style="color:#B22222"> '''''lox5171'' Reverse in pSB1A2''' </span>  || <span style="color:#B22222"> This plasmid will also be sent off for sequencing soon.  ||  [http://partsregistry.org/Part:pSB1A2] </span> <br> <span style="color:#B22222"> ''lox5171'' does not exist in the registry.  We ordered oligos and constructed the site in the lab. </span> || Nitya
+
|<span style="color:#B22222"> '''''lox5171'' Reverse in pSB1A2''' </span>  || <span style="color:#B22222"> This plasmid will also be sent off for sequencing soon.  ||  [http://partsregistry.org/Part:pSB1A2 pSB1A2] </span> <br> <span style="color:#B22222"> ''lox5171'' does not exist in the registry.  We ordered oligos and constructed the site in the lab. </span> || Nitya
 
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!width="30"|Primary Team Member
 
!width="30"|Primary Team Member
 
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|<span style="color:#B22222"> '''I718008 (pBAD+RBS+cre) in pSB4K5''' </span>  || <span style="color:#B22222"> At this point, I have isolated both the insert and the plasmid, but my two attempts at ligation have not produced any colonies.  ||  [http://partsregistry.org/Part:BBa_I718008] [http://partsregistry.org/wiki/index.php?title=Part:pSB4K5]</span> <br> <span style="color:#B22222"> </span> || Nitya
+
|<span style="color:#B22222"> '''I718008 (pBAD+RBS+cre) in pSB4K5''' </span>  || <span style="color:#B22222"> At this point, I have isolated both the insert and the plasmid, but my two attempts at ligation have not produced any colonies.  ||  [http://partsregistry.org/Part:BBa_I718008 I718008] [http://partsregistry.org/wiki/index.php?title=Part:pSB4K5 pSB4K5]</span> <br> <span style="color:#B22222"> </span> || Nitya
 
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Revision as of 15:49, 15 June 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

Biology Sub-Projects

Codon Optimization



Tet-trations



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
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


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
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
Insert Info Here what is built so far? change to correct link
describe intermediate
your name here