Team:UQ-Australia/Data

From 2011.igem.org

(Difference between revisions)
Line 1: Line 1:
{{:Team:UQ-Australia/Template:Header}}
{{:Team:UQ-Australia/Template:Header}}
-
{|align="justify"
+
{|style="width:100%;" border="0" cellpadding="10" cellspacing="0"  
-
|You can write a background of your team here.  Give us a background of your team, the members, etc.  Or tell us more about something of your choosing.
+
|rowspan="2"|There is a '[HERE]'where you should edit in places where I remembered to put them.
-
|[[File:IGEM basic Logo stylized.png|125x125px|link=https://2011.igem.org]]
+
[HERE] Summary [HERE]
 +
! width="125" |[[File:IGEM basic Logo stylized.png|125x125px|link=https://2011.igem.org]]
|-
|-
-
|
 
-
''Tell us more about your project.  Give us background.  Use this is the abstract of your project.  Be descriptive but concise (1-2 paragraphs)''
 
|[[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]]
-
|
 
|}
|}

Revision as of 12:00, 4 October 2011




There is a '[HERE]'where you should edit in places where I remembered to put them.

[HERE] Summary [HERE]

IGEM basic Logo stylized.png
UQ-Australia logo 2011.png

We conducted a heat cycle PCR to determine the optimum conditions for amplifying our araC gene. The lanes here are loaded as follows:

1: 1kb+ ladder

2: Negative control (H2O)

3-7: pBAD33 plasmid at temperatures 50C, 55C, 58C, 60C and 65C.

8: Negative control (H2O)

9-13: pBAD33 plasmid at temperatures 50C, 55C, 58C, 60C and 65C.

IMG 0190.JPG