Difference between revisions of "Part:BBa J01010:Experience"
(→User Reviews) |
|||
| Line 18: | Line 18: | ||
|}; | |}; | ||
<!-- End of the user review template --> | <!-- End of the user review template --> | ||
| + | <!-- DON'T DELETE --><partinfo>BBa_J01010 EndReviews</partinfo> | ||
| + | |||
{|width='80%' style='border:1px solid gray' | {|width='80%' style='border:1px solid gray' | ||
|- | |- | ||
|width='10%'| | |width='10%'| | ||
| − | <partinfo> | + | <partinfo>BBa_J01008 AddReview 5</partinfo> |
| − | <I> | + | <I>HZAU-China 2014</I> |
|width='60%' valign='top'| | |width='60%' valign='top'| | ||
| − | + | We want to know under the participation of taRNA and crRNA, whether can reduce leakage of lac promoter’s expression. So we did some experiment to text. First, built the tow devices and from top to bottom Numbers for 1 2 , and then, respectively transform the three plasmid into BL21 competent cell. Pick monoclonal colony. Add 5ml LB liquid and incubate at 37 Celsius degree for 8 hours. Secondly, add 5ul of E.coli liquid cultural medium from each tube to two new tubes named A, B respectively with 5ml M9 broth in it. Add 0.1ul IPTG to all A tubes (1A, 2A, ) while add nothing to all B tubes (1B, 2B, ). Incubating at 37 Celsius degree for 4 hours. Lastly, easuring the fluorescent degree by utilizing the enzyme-labeled instrument. | |
| + | Conclusion : riboregulators ensure much lower leakage of the promoters. | ||
| + | |||
| + | [[File:HZAU2014-图片1.jpg|700px|right]] | ||
| + | [[File:HZAU2014-图片2.jpg|600px|centre]] | ||
| + | [[File:HZAU2014-ribo.jpg|700px]] | ||
|} | |} | ||
| − | <!-- | + | <!-- End of the user review template --> |
Revision as of 06:38, 17 October 2014
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_J01010
User Reviews
UNIQc4eae457467b44e0-partinfo-00000000-QINU UNIQc4eae457467b44e0-partinfo-00000001-QINU
|
•••••
HZAU-China 2014 |
We want to know under the participation of taRNA and crRNA, whether can reduce leakage of lac promoter’s expression. So we did some experiment to text. First, built the tow devices and from top to bottom Numbers for 1 2 , and then, respectively transform the three plasmid into BL21 competent cell. Pick monoclonal colony. Add 5ml LB liquid and incubate at 37 Celsius degree for 8 hours. Secondly, add 5ul of E.coli liquid cultural medium from each tube to two new tubes named A, B respectively with 5ml M9 broth in it. Add 0.1ul IPTG to all A tubes (1A, 2A, ) while add nothing to all B tubes (1B, 2B, ). Incubating at 37 Celsius degree for 4 hours. Lastly, easuring the fluorescent degree by utilizing the enzyme-labeled instrument. Conclusion : riboregulators ensure much lower leakage of the promoters.  
|
