IGEM:University of East Anglia (UEA), Norwich, UK/2009/Notebook/NRP-UEA-Norwich iGEM/2013/08/16

From OpenWetWare

(Difference between revisions)
Jump to: navigation, search
(Entry title)
Line 5: Line 5:
|-
|-
| colspan="2"|
| colspan="2"|
-
==Entry title==
+
==Floor Two==
-
* Insert your content here.
+
The two overnight cultures, containing BL21 cells that had been transformed with Pet28AntA were retrieved. Culture 1a was used to make competent cells, while sample 1b was induced with IPTG and left to incubate at 25°C overnight. While the cells were growing, minipreps of BL21 PlySs and BL21 rosetta PlySs cultures were prepared and stored in the freezer. <br>
 +
The BL21 Pet28AntA competent cells were transformed with the biobrick BBa_K1041002 (AntG promoter + RFP gene) and spread onto a LB Agar plate containing Kanamycin and Chlorophenicol antibiotics and six control plates were prepared ''fig''

Revision as of 09:19, 16 August 2013

Week Eleven Main project page
Previous entry      Next entry

Floor Two

The two overnight cultures, containing BL21 cells that had been transformed with Pet28AntA were retrieved. Culture 1a was used to make competent cells, while sample 1b was induced with IPTG and left to incubate at 25°C overnight. While the cells were growing, minipreps of BL21 PlySs and BL21 rosetta PlySs cultures were prepared and stored in the freezer.
The BL21 Pet28AntA competent cells were transformed with the biobrick BBa_K1041002 (AntG promoter + RFP gene) and spread onto a LB Agar plate containing Kanamycin and Chlorophenicol antibiotics and six control plates were prepared fig



Personal tools