Difference between revisions of "Part:BBa E0040:Experience"
(→User Reviews) |
(→User Reviews) |
||
Line 24: | Line 24: | ||
<I>KAIST_iGEM_2012</I> | <I>KAIST_iGEM_2012</I> | ||
|width='60%' valign='top'| | |width='60%' valign='top'| | ||
− | [[image: KAIST_iGEM_2012_Experience_BBa_E0040.PNG|center|thumb|400px|'''Figure 1. E.coli strain MG1655 expressing BBa_E0040 under control of <partinfo>BBa_K907004</partinfo> after overnight culture. 3mL M9 media | + | [[image: KAIST_iGEM_2012_Experience_BBa_E0040.PNG|center|thumb|400px|'''Figure 1. E.coli strain MG1655 expressing BBa_E0040 under control of <partinfo>BBa_K907004</partinfo> after overnight culture. 3mL culture with M9 media in 14 mL round bottom tube(Top left two) and centrifuged cells in eppendorf tube(Bottom left two).''' The expression of BBa_0040 is clearly observed with naked eye after overnight culture.]] |
<br><partinfo>BBa_E0040</partinfo> was successfully used to produce GFPmut3b in E.coli strain MG1655 in LB or M9 minimal media under the control of promoter-<partinfo>BBa_J23119</partinfo> and RBS-<partinfo>BBa_B0034</partinfo> in the Dual Phase Protein Generator(GFP default), <partinfo>BBa_K907004</partinfo>. | <br><partinfo>BBa_E0040</partinfo> was successfully used to produce GFPmut3b in E.coli strain MG1655 in LB or M9 minimal media under the control of promoter-<partinfo>BBa_J23119</partinfo> and RBS-<partinfo>BBa_B0034</partinfo> in the Dual Phase Protein Generator(GFP default), <partinfo>BBa_K907004</partinfo>. | ||
Revision as of 23:30, 26 September 2012
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_E0040
User Reviews
UNIQfc356483ce207d74-partinfo-00000000-QINU
••
KAIST_iGEM_2012 |
|
•••••
Antiquity |
This review comes from the old result system and indicates that this part worked in some test. |
UNIQfc356483ce207d74-partinfo-00000008-QINU
E0040 contains 2 dpnI sites. This is useful when using a part containing E0040 as a template for PCR because you can cut up the template via a dpnI digest. For this to work the cell strain that the template was purified from must be dam methylase+.
iGEM11_WHU_China |
This part was used by WHU_China team as a reporter of long-term oscillator. Information from the website of this part shows that its length is about 720bp; however, the result of restriction enzymes cleavage experiment showed that it is actually about 1kb. And after several attempts, we failed to assemble this part with other biobricks. |