Team:UQ-Australia/Notebook/July

From 2011.igem.org

(Difference between revisions)
 
(One intermediate revision not shown)
Line 1: Line 1:
{{:Team:UQ-Australia/Template:Header}}
{{:Team:UQ-Australia/Template:Header}}
-
 
-
 
{|style="width:100%;" border="0" cellpadding="10" cellspacing="0"  
{|style="width:100%;" border="0" cellpadding="10" cellspacing="0"  
 +
|- valign="top"
|rowspan="2"|During July, we continued to optimize our lab protocols, particularly the PCR conditions to add on our BioBrick ends. This was met with moderate success, while most of our cloning still did not go as planned.  
|rowspan="2"|During July, we continued to optimize our lab protocols, particularly the PCR conditions to add on our BioBrick ends. This was met with moderate success, while most of our cloning still did not go as planned.  
-
! width="125" |[[File:IGEM basic Logo stylized.png|125x125px|link=https://2011.igem.org]]
+
! [[File:UQ-Australia_logo_2011.png|125x125px|link=https://2011.igem.org/Team:UQ-Australia]]
-
|-
+
-
|[[File:UQ-Australia_logo_2011.png|125x125px|link=https://2011.igem.org/Team:UQ-Australia]]
+
|}
|}
-
 

Latest revision as of 00:45, 6 October 2011




During July, we continued to optimize our lab protocols, particularly the PCR conditions to add on our BioBrick ends. This was met with moderate success, while most of our cloning still did not go as planned. UQ-Australia logo 2011.png


Summary of Lab Work

We conducted a number of heat-cycle PCRs to find the optimal conditions to amplify the lacI and araC genes. These tests were promising and we were able to get a lacI sample at 16.3ng/ul

However, our other lab work did not progress well, with none of the cloning of the parts we had synthesized working.

Retrieved from "http://2011.igem.org/Team:UQ-Australia/Notebook/July"