Difference between revisions of "Part:BBa K1074006:Experience"
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− | <partinfo>BBa_K1074006 AddReview | + | <partinfo>BBa_K1074006 AddReview 3</partinfo> |
<I>USTC_China iGEM13</I> | <I>USTC_China iGEM13</I> | ||
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− | + | In our project, we construct other four gene circuits based on this part. In these gene circuits, GFP is replaced by HBsAg, Ag85b, PAD4, LTB respectively. We transformed the recombinant | |
+ | Plasmids both in BL21 and Bacillus Subtilis WB800N and induced expression with IPTG . Results analyzed by SDS-page , mass spectrum and ELISA were proved positive. But proteins expressed in WB800N were far less than those in BL21. The antigenicity and transdermal function of N-terminal TD1 modified antigen HBsAg was also tested positive by ELISA. | ||
+ | [[Image:USTC_China_iGEM13_BBa_K1074006_1.png|thumb|left|800px|figure 1 SDS-PAGE of N-terminal TD1 modified GFP]] | ||
+ | [[Image:USTC_China_iGEM13_BBa_K1074006_4.png|thumb|left|800px|figure 2 SDS-PAGE of N-terminal TD1 modified LTB and HBsAg]] | ||
+ | [[Image:USTC_China_iGEM13_BBa_K1074006_2.JPG|thumb|left|600px|figure 3 Fluorescence detection of N-terminal TD1 modified GFP expression with and without IPTG induction]] | ||
+ | [[Image:USTC_China_iGEM13_BBa_K1074006_5.jpg|thumb|left|800px|figure 4 ELISA test transdermal function of N-terminal TD1 modified antigen HBsAg ]] | ||
+ | |||
|}; | |}; |
Revision as of 13:09, 27 September 2013
This experience page is provided so that any user may enter their experience using this part.
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how you used this part and how it worked out.
Applications of BBa_K1074006
User Reviews
UNIQe89a052b2154d9d0-partinfo-00000000-QINU UNIQe89a052b2154d9d0-partinfo-00000001-QINU
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USTC_China iGEM13 |
In our project, we construct other four gene circuits based on this part. In these gene circuits, GFP is replaced by HBsAg, Ag85b, PAD4, LTB respectively. We transformed the recombinant Plasmids both in BL21 and Bacillus Subtilis WB800N and induced expression with IPTG . Results analyzed by SDS-page , mass spectrum and ELISA were proved positive. But proteins expressed in WB800N were far less than those in BL21. The antigenicity and transdermal function of N-terminal TD1 modified antigen HBsAg was also tested positive by ELISA. |