Difference between revisions of "Part:BBa K772100:Experience"

 
Line 18: Line 18:
 
After the correct ligation and cloning procedures, we extracted both bacterial and tumor cell protein ingredients via performing sonication. Affinity Gel Chromatography is performed on bacterial protein extract in order to isolate our EpCAM binding docks. These docks were exposed to tumor cell extract; thus the binding would occur. SDS-PAGE is done aftermath on the last solution. <br><br>
 
After the correct ligation and cloning procedures, we extracted both bacterial and tumor cell protein ingredients via performing sonication. Affinity Gel Chromatography is performed on bacterial protein extract in order to isolate our EpCAM binding docks. These docks were exposed to tumor cell extract; thus the binding would occur. SDS-PAGE is done aftermath on the last solution. <br><br>
  
https://static.igem.org/mediawiki/2012/archive/f/f7/20120927035038!Sherlocoli_Overview_%281%29.png https://static.igem.org/mediawiki/igem.org/archive/e/e0/20120927030300!20120925_161036.jpg
+
[[Image:Res1.jpg]] [[Image:Res2.jpg]]
  
  

Latest revision as of 08:37, 5 October 2012


• EpCAM binding docks are cloned and confirmed. The gene sequences of EpCAM binding docks are synthesized particularly and separately. The confirmation electrophoresis and PCR afterwards were found correct. BBa_K772001 and BBa_K772002 are fixed together via 3A assembly method. After transformation into E.coli, the gel bands match with their original length; therefore we proceeded to the next step: Sequencing.

20120927030036!20120925_161036.jpg 20120927030055!20120925_161036.jpg


• Binding docks are sequenced and found correct. Sequence results overlap with the original sequences and show that these two parts are assembled correctly and ready to test for the synthesis and its function.



Sekans.png

• Binding docks are synthesized and are able to bind to the EpCAM. After the correct ligation and cloning procedures, we extracted both bacterial and tumor cell protein ingredients via performing sonication. Affinity Gel Chromatography is performed on bacterial protein extract in order to isolate our EpCAM binding docks. These docks were exposed to tumor cell extract; thus the binding would occur. SDS-PAGE is done aftermath on the last solution.

Res1.jpg Res2.jpg


Applications of BBa_K772100

User Reviews

UNIQb3f192ad6eca3692-partinfo-00000000-QINU UNIQb3f192ad6eca3692-partinfo-00000001-QINU