Team:Warsaw/Calendar-Stage1/7 July 2010

From 2010.igem.org

(Difference between revisions)
(New page: <html> <script type="text/javascript"> ActiveTab='WetLab'; </script> </html> {{TemplateTop}} {{UpperTabs}} {{LowerTabsTeam}} <html> <!-- do not edit above me! --> <br> 07.07.2010 Wednesd...)
 
Line 16: Line 16:
<br> 1. Cultures from 6.07.2010 were centrifuged -> sediments in the eppendorfs were light green.
<br> 1. Cultures from 6.07.2010 were centrifuged -> sediments in the eppendorfs were light green.
-
<br> 2. Transformation results from 6.07.2010: individual clones were green during exposition to UV light.
+
<br> 2. Alkaline lysis of these 'green cultures'.
-
<br> 3. Set up 2 ml liquid cultures of 'green' clones GFP-terminator/Anderson's RBS.
+
<br> 3. Inoculation of Petri plates with ampicillin.
-
<br> 4. Set up 2 ml liquid cultures of 15-20 random clones from each plate.
+
<br>
-
 
+
<br> -> Transformation results from 6.07.2010: clones were green during exposition to UV light -> we inoculated the plates with ampicillin.
 +
<br>
 +
<br><div class="note">Cloning GFP-terminator behind RBSes - approach 2. [Ania S., Ania P., Kasia, Cherry] </div>
 +
<br> 1. Clones obtained on the plates after transformation were used to set up liquid cultures (per 2 ml). We've got 10-20 tubes with cultures from each plate (B0030/GFP = our number 7, B0031/GFP = our number 8, B0032/GFP = our number 9, B0033/GFP = our number 10, B0034/GFP = our number 11) 

Latest revision as of 14:56, 31 July 2010

Example Tabs


07.07.2010 Wednesday

Cloning GFP-terminator behind RBSes - approach 1 [Ania S., Ania P., Kasia, Cherry]

1. Cultures from 6.07.2010 were centrifuged -> sediments in the eppendorfs were light green.
2. Alkaline lysis of these 'green cultures'.
3. Inoculation of Petri plates with ampicillin.

-> Transformation results from 6.07.2010: clones were green during exposition to UV light -> we inoculated the plates with ampicillin.

Cloning GFP-terminator behind RBSes - approach 2. [Ania S., Ania P., Kasia, Cherry]

1. Clones obtained on the plates after transformation were used to set up liquid cultures (per 2 ml). We've got 10-20 tubes with cultures from each plate (B0030/GFP = our number 7, B0031/GFP = our number 8, B0032/GFP = our number 9, B0033/GFP = our number 10, B0034/GFP = our number 11)