IGEM:Groningen/Notebook/iGEM 2011/2011/06/24: Difference between revisions

From OpenWetWare
Jump to navigationJump to search
(Autocreate 2011/06/24 Entry for IGEM:Groningen/Notebook/iGEM_2011)
 
Line 6: Line 6:
| colspan="2"|
| colspan="2"|
<!-- ##### DO NOT edit above this line unless you know what you are doing. ##### -->
<!-- ##### DO NOT edit above this line unless you know what you are doing. ##### -->
==Entry title==
==24-6-11==
* Insert content here...


<br>
<br> Purify the PCR product with the High Pure PCR Purification kit from Roche
<br> PhybB-RBS-GFP-DT
<br>
<br> Digestion mix:
<br> 18μl buffer
<br> 4.5μl EcoRI
<br> 4.5μl SpeI
<br> 49μl MQ water
<br>
<br> Vector mix:
<br> 18μl buffer
<br> 4.5μl EcoRI
<br> 4.5μl XbaI
<br> 49μl MQ water
<br>
<br> Ligation:
<br> 2μl T4 DNA ligase buffer
<br> 1μl T4 DNA ligase
<br> 7μl insert
<br> 3μl vector
<br> 7μl MQ water
<br>
<br> Ligate 2 hours at room temperature
<br>
<br> Transformation
<br> Add to 40μl competent cells 10μl ligation mixture
<br> Incubate for 30 min on ice
<br> Heat shock: 45s at 42 degrees
<br> Incubate cells on ice for 2 min
<br> Add 1ml LB medium+ 25mM glucose
<br> Incubate cells for 1h/1.5h at 37 degrees
<br> Spin the cells down, resuspend them in 100μl LB medium and plate 90μl and 10μl out on the plates
<br> Put the plates in the stove at 37 degrees overnight


<!-- ##### DO NOT edit below this line unless you know what you are doing. ##### -->
<!-- ##### DO NOT edit below this line unless you know what you are doing. ##### -->

Revision as of 03:39, 21 September 2011

Project name <html><img src="/images/9/94/Report.png" border="0" /></html> Main project page
<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>Previous entry<html>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</html>Next entry<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>

24-6-11



Purify the PCR product with the High Pure PCR Purification kit from Roche
PhybB-RBS-GFP-DT

Digestion mix:
18μl buffer
4.5μl EcoRI
4.5μl SpeI
49μl MQ water

Vector mix:
18μl buffer
4.5μl EcoRI
4.5μl XbaI
49μl MQ water

Ligation:
2μl T4 DNA ligase buffer
1μl T4 DNA ligase
7μl insert
3μl vector
7μl MQ water

Ligate 2 hours at room temperature

Transformation
Add to 40μl competent cells 10μl ligation mixture
Incubate for 30 min on ice
Heat shock: 45s at 42 degrees
Incubate cells on ice for 2 min
Add 1ml LB medium+ 25mM glucose
Incubate cells for 1h/1.5h at 37 degrees
Spin the cells down, resuspend them in 100μl LB medium and plate 90μl and 10μl out on the plates
Put the plates in the stove at 37 degrees overnight