Team:OUC-China/Result/week12
From 2011.igem.org
9-26
Extract the plasmids of 14-19 and RFP and detect their concentrations.
Pick out the bacteria colony of J13002 into LB medium.
The plates which are used for standerdizing 18-3-11,14-19,5-4,rhiABCpro,13-6-leu and 18-3-11-6-leuB have already bacteria. And we select some into LB.
Double-enzyme cut RFP, rhiR,14-19-13 and LeuB with EcoRI and PstI. We recover them with gel extraction mini kit after electrophoresis.
Standerdize the part—rhiI. Transform C0076&6、E0020&6、5-4&6-leuB and coat them on square plates. Then ligate rhiR&RFP, leuB&carrier C, 14-19-13&carrier C.
9-27
Preservate the strains of J13002 and extract the plasmids. Circuit-I’s standerdization failed. We go on cleavaging, ligating and transforming. At the same time we extract the plasmids of 18-3-11、14-19、5&4、rhiABCpro、13&6-leuB、18-3-11&6-leuB. But the plasmids of 14-19 go red because of ligating themselves. We have to lay it down.
We put one preservation tube of every strain into -80℃.
Four parts transformed yesterday failed.(so many failures…oh no>..<) Transform the standardized parts of rhiI、14-19-13、leuB、rhiR. Verify the standardized parts by double-enzyme cleavaging.
Make some solid medium. The resistance are K and T.
In the evening, we cut RFP (to be standardized),14-19(to be standardized), J13002(to be verified) and 6-leuB(to be 6-leuB).