Difference between revisions of "Part:BBa K1074006:Experience"

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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
 
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.
 
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.
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[[Image:USTC_China_iGEM13_BBa_K1074006_1.png|thumb|left|300px|figure 1 SDS-PAGE of N-terminal TD1 modified GFP]]
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[[Image:USTC_China_iGEM13_BBa_K1074006_4.png|thumb|right|300px|figure 2 SDS-PAGE of N-terminal TD1 modified LTB and HBsAg]]
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[[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]]
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[[Image:USTC_China_iGEM13_BBa_K1074006_5.jpg|thumb|left|600px|figure 4 ELISA test transdermal function of N-terminal TD1 modified antigen HBsAg ]]
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Latest revision as of 17:23, 27 September 2013


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Applications of BBa_K1074006

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UNIQ3426d3b7ce6fd1b0-partinfo-00000000-QINU UNIQ3426d3b7ce6fd1b0-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.


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