Difference between revisions of "Part:BBa K2859000:Experience"

Revision as of 03:04, 18 October 2018

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Applications of BBa_K2859000

User Reviews

UNIQ3d8fe72c88793620-partinfo-00000000-QINU UNIQ3d8fe72c88793620-partinfo-00000001-QINU

We synthesised the part flanked by bioBrick prefix and suffix. Then, the synthesized gblock was ligated into pSB1C3 by restriction digest with EcoR1 and Pst1 and transformed into E.Coli DH5-α.We confirmed that the ligation was successfully done by running gel with minicprepped DNA cut with EcoR1 (about 2.4kb). The transformed E.coli was grown at 37°C. The expression of Penetratin-Insulin-Flag tag complex was evaluated by SDS page gel.

Figure1. 1.2% Agarose Gel electrophoresis result of pSB1C3 cut with EcoR1

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-We synthesised the part flanked by bioBrick prefix and suffix. Then, the synthesized gblock was ligated into pSB1C3 by restriction digest with EcoR1 and Pst1 and transformed into E.Coli DH5-α.The transformed E.coli was grown at 37°C. The expression of Penetratin-Insulin-Flag tag complex was evaluated by SDS page gel.
+We synthesised the part flanked by bioBrick prefix and suffix. Then, the synthesized gblock was ligated into pSB1C3 by restriction digest with EcoR1 and Pst1 and transformed into E.Coli DH5-α.We confirmed that the ligation was successfully done by running gel with minicprepped DNA cut with EcoR1 (about 2.4kb). The transformed E.coli was grown at 37°C. The expression of Penetratin-Insulin-Flag tag complex was evaluated by SDS page gel.
+Figure1. 1.2% Agarose Gel electrophoresis result of pSB1C3 cut with EcoR1
 https://res.cloudinary.com/dt6jjveot/image/upload/SDS.jpg