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

Latest revision as of 03:23, 18 October 2018

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Please enter how you used this part and how it worked out.

Applications of BBa_K2859000

User Reviews

UNIQfa6b4297046d50ee-partinfo-00000000-QINU UNIQfa6b4297046d50ee-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 2.5kb). 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

Figure2. 10% SDS page gel result showing the expression of protein

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 <!-- DON'T DELETE --><partinfo>BBa_K2859000 EndReviews</partinfo>
-https://res.cloudinary.com/dt6jjveot/image/upload/SDSpage.jpg
+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 2.5kb). The transformed E.coli was grown at 37°C. The expression of Penetratin-Insulin-Flag tag complex was evaluated by SDS page gel.
+https://static.igem.org/mediawiki/2018/8/81/T--HAFS--partgel3.png
+Figure1. 1.2% Agarose Gel electrophoresis result of pSB1C3 cut with EcoR1
+https://res.cloudinary.com/dt6jjveot/image/upload/SDS.jpg
+Figure2. 10% SDS page gel result showing the expression of protein