Difference between revisions of "Part:BBa J364000:Experience"

Revision as of 08:39, 17 October 2018

This experience page is provided so that any user may enter their experience using this part.
Please enter how you used this part and how it worked out.

Applications of BBa_J364000

User Reviews

UNIQaa66cb98c6d73e42-partinfo-00000000-QINU UNIQaa66cb98c6d73e42-partinfo-00000001-QINU

SCU-China 2018:

Experiment conditions:1. 37℃ incubator for bacteria; 2.LB liquid medium. We use this part (BBa_J364000) as our original source of GFP proteins. As our expectation, this part can work normally under our experiment conditions. For the modification, we added a spacer sequence and NGG site just on the upstream of the promoter for repression of GFP expression. And this modification is very successful because the supression is obvious according to the Figure 1 below. As the picture shows, the part:BBa_J364000 and our part: BBa_K2611001 can both function well. And for the improvement: this part's expression can be regulated under the control of dCas9 system.

2017 Georgia State iGEM Team

Georgia State Growth Medium Study

Mean Fluorescence Intensity measured by flow cytometry of GFP expressed from 6-hour cultures of BBa_J364000 in multiple growth mediums.

@@ Line 21: / Line 21: @@
 SCU-China 2018:
-<b>Experiment conditions:</b>1. 37℃ incubator for bacteria; 2.LB liquid medium.
+<p><b>Experiment conditions:</b>1. 37℃ incubator for bacteria; 2.LB liquid medium.
 We use this part (BBa_J364000) as our original source of GFP proteins. As our expectation, this part can work normally under our experiment conditions.
 For the modification, we added a spacer sequence and NGG site just on the upstream of the promoter for repression of GFP expression. And this   modification is very successful because the supression is obvious according to the Figure 1 below.