Team:Calgary/1 July 2010

From 2010.igem.org

(Difference between revisions)
Line 1: Line 1:
{{CalgaryNotebookTemplate|
{{CalgaryNotebookTemplate|
'''Thursday July 1, 2010'''
'''Thursday July 1, 2010'''
 +
<i>Happy Canada Day!!</i>
<i>Happy Canada Day!!</i>
-
Himika: Today I transformed composite parts from the registry I03504 and I03507. These parts basically comprise of RBS(B0034)-GFP/RFP(E0040/E1010)-terminator (B0015). Both these parts were plated on ampicillin. I03504 gave mats on the ampicillin plates and I03507 gave clear colonies. These colonies would later be screened to make sure parts are in there using Biobrick PCR primers and gel electrophoresis.
+
<u>Himika</u>
 +
 
 +
Today I transformed composite parts from the registry I03504 and I03507. These parts basically comprise of RBS(B0034)-GFP/RFP(E0040/E1010)-terminator (B0015). Both these parts were plated on ampicillin. I03504 gave mats on the ampicillin plates and I03507 gave clear colonies. These colonies would later be screened to make sure parts are in there using Biobrick PCR primers and gel electrophoresis.
 +
 
 +
 
 +
<u>Patrick</u>
 +
 
 +
I ran another gel of the ''cpxP'' digest, though it turned out a little bit less than what we had hoped it would look. We also ran a gel of a PCR of the ''cpxP'' plasmid by itself, using the original gene-specific primers with BioBrick sites, in order to see if we could PCR out a section of the DNA that corresponded to the ''cpxP'' site.
 +
 
}}
}}

Revision as of 19:24, 7 July 2010

Thursday July 1, 2010


Happy Canada Day!!

Himika

Today I transformed composite parts from the registry I03504 and I03507. These parts basically comprise of RBS(B0034)-GFP/RFP(E0040/E1010)-terminator (B0015). Both these parts were plated on ampicillin. I03504 gave mats on the ampicillin plates and I03507 gave clear colonies. These colonies would later be screened to make sure parts are in there using Biobrick PCR primers and gel electrophoresis.


Patrick

I ran another gel of the cpxP digest, though it turned out a little bit less than what we had hoped it would look. We also ran a gel of a PCR of the cpxP plasmid by itself, using the original gene-specific primers with BioBrick sites, in order to see if we could PCR out a section of the DNA that corresponded to the cpxP site.

No notebook page exists for this date. Sorry!