31 May 31, 2012

From 2012.igem.org

(Difference between revisions)

Latest revision as of 23:28, 1 June 2012

Week 1

YLC collaboration: WashU iGEM has decided to conduct an outreach project in collaboration with [http://www.ylc-stl.org/ The Youth Learning Center(YLC)] here in St. Louis. The aim of this project is to introduce 6th to 8th graders to synthetic biology. In doing so, we hope to educate the students about the power of this new technology and the the real challenges and concerns associated with it. How well we achieve this goal will be measured by giving a brief survey before and after our two days with the students. We will use the result of the project to make a series of short educational videos covering similar material that will be free to the public.

This week we have begun the project by transforming E. coli with the following biobricks:

1. eYFP: [http://www.google.com/url?q=http%3A%2F%2Fpartsregistry.org%2Fwiki%2Findex.php%3Ftitle%3DPart%3ABBa_E0430&sa=D&sntz=1&usg=AFQjCNGQMpvic9Hi4iih_Ayd4jQd0fDmSQ Part:BBa_E0430]

2. GFP: [http://www.google.com/url?q=http%3A%2F%2Fpartsregistry.org%2Fwiki%2Findex.php%3Ftitle%3DPart%3ABBa_E0430&sa=D&sntz=1&usg=AFQjCNGQMpvic9Hi4iih_Ayd4jQd0fDmSQ Part:BBa_I13504]

3. mRFP: [http://www.google.com/url?q=http%3A%2F%2Fpartsregistry.org%2Fpartsdb%2Fget_part.cgi%3Fpart%3DBBa_I13507&sa=D&sntz=1&usg=AFQjCNF9ZnOYMi4BC6Yjua5Vli5l5kewfA Part:BBa_I13507]

4. eCFP: [http://www.google.com/url?q=http%3A%2F%2Fpartsregistry.org%2Fwiki%2Findex.php%3Ftitle%3DPart%3ABBa_E0420&sa=D&sntz=1&usg=AFQjCNGqh4nrV86rOPlesY61Pf7iLz8FNA Part:BBa_E0420]

5.Promoter: [http://www.google.com/url?q=http%3A%2F%2Fpartsregistry.org%2FPart%3ABBa_J23100&sa=D&sntz=1&usg=AFQjCNELvuUsDOxN_7JUN2LmvFEozGQRnw Part:BBa_J23100]

Each gene had at least one successful transformation. The colony counts were as follows:

Gene	450μL	900μL
1	5	0
2	0	3
3	0	1
4	1	0
5	7	36

Synechocystis Saffron:

This week we have focused on finalizing the design of the gene before submitting it to [http://www.google.com/url?q=http%3A%2F%2Fwww.idtdna.com%2Fsite&sa=D&sntz=1&usg=AFQjCNGgX2far85q9ockLj4SZJPHmbdSiA IDT] for synthesis. One major modification we have made is the insertion of restriction sites between the three open reading frames of our genes. We hope that this will be helpful if we need to rearrange the genes or insert elements between them to maximize the production of our target products. The details of our final gene as well as the annotated version of our plasmid can be viewed at our projects page.

@@ Line 6: / Line 6: @@
 <font size="2.8">
-YLC collaboration:
+'''YLC collaboration:'''
-WashU iGEM has decided to conduct an outreach project in collaboration with the Youth Learning Center (YLC) here in St. Louis.  The aim of this project is to introduce 6th to 8th graders to synthetic biology.  In doing so, we hope to educate the students about the power of this new technology and the the real challenges and concerns associated with it.  How well we achieve this goal will be measured by giving a brief survey before and after our two days with the students. We will use the result of the project to make a series of short educational videos covering similar material that will be free to the public.  A first draft of our YLC teaching plan can be viewed here:  (link).
+WashU iGEM has decided to conduct an outreach project in collaboration with [http://www.ylc-stl.org/ The Youth Learning Center(YLC)] here in St. Louis.  The aim of this project is to introduce 6th to 8th graders to synthetic biology.  In doing so, we hope to educate the students about the power of this new technology and the the real challenges and concerns associated with it.  How well we achieve this goal will be measured by giving a brief survey before and after our two days with the students. We will use the result of the project to make a series of short educational videos covering similar material that will be free to the public.
-This week we have begun the project by transforming E. coli with the following biobricks:
+This week we have begun the project by transforming ''E. coli'' with the following biobricks:
-. eYFP: Part:BBa_E0430
+. eYFP: [http://www.google.com/url?q=http%3A%2F%2Fpartsregistry.org%2Fwiki%2Findex.php%3Ftitle%3DPart%3ABBa_E0430&sa=D&sntz=1&usg=AFQjCNGQMpvic9Hi4iih_Ayd4jQd0fDmSQ Part:BBa_E0430]
-. GFP:Part:BBa_I13504
+. GFP: [http://www.google.com/url?q=http%3A%2F%2Fpartsregistry.org%2Fwiki%2Findex.php%3Ftitle%3DPart%3ABBa_E0430&sa=D&sntz=1&usg=AFQjCNGQMpvic9Hi4iih_Ayd4jQd0fDmSQ Part:BBa_I13504]
-. mRFP: Part:BBa_I13507:Get Part
+. mRFP: [http://www.google.com/url?q=http%3A%2F%2Fpartsregistry.org%2Fpartsdb%2Fget_part.cgi%3Fpart%3DBBa_I13507&sa=D&sntz=1&usg=AFQjCNF9ZnOYMi4BC6Yjua5Vli5l5kewfA Part:BBa_I13507]
-. eCFP: Part:BBa_E0420
+. eCFP: [http://www.google.com/url?q=http%3A%2F%2Fpartsregistry.org%2Fwiki%2Findex.php%3Ftitle%3DPart%3ABBa_E0420&sa=D&sntz=1&usg=AFQjCNGqh4nrV86rOPlesY61Pf7iLz8FNA Part:BBa_E0420]
-.Promoter: Part:BBa_J23100
+.Promoter: [http://www.google.com/url?q=http%3A%2F%2Fpartsregistry.org%2FPart%3ABBa_J23100&sa=D&sntz=1&usg=AFQjCNELvuUsDOxN_7JUN2LmvFEozGQRnw Part:BBa_J23100]
-Each type individual gene had at least one successful transformation.  The colony counts were as follows:
+Each gene had at least one successful transformation.  The colony counts were as follows:
 <table border="1">
@@ Line 57: / Line 57: @@
+'''Synechocystis Saffron:'''
-Synechocystis Saffron:
+This week we have focused on finalizing the design of the gene before submitting it to [http://www.google.com/url?q=http%3A%2F%2Fwww.idtdna.com%2Fsite&sa=D&sntz=1&usg=AFQjCNGgX2far85q9ockLj4SZJPHmbdSiA IDT] for synthesis.  One major modification we have made is the insertion of restriction sites between the three open reading frames of our genes.  We hope that this will be helpful if we need to rearrange the genes or insert elements between them to maximize the production of our target products.  The details of our final gene as well as the annotated version of our plasmid can be viewed at our projects page.
-This week has focused on finalizing the design of the gene before submitting it to IDT for synthesis.  One major modification we have made is the insertion of restriction sites between the three open reading frames of our genes.  We hope that this will be helpful if we need to rearrange the genes or insert elements between them to maximize the production of our target products.  The details of our final gene as well as the annotated version of our plasmid can be viewed at our projects page.