Difference between revisions of "Part:BBa K1202100:Experience"

 
 
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Firstly we wanted to test that can our bacteria produce C215 (Anti-EpCAM). To test this, we did Immunofluorescence experiments. We put OmpA (a signal peptide which send proteins to membrane) signal peptide sequence and his-tag sequence before C215 protein sequence in our one part. And then we did immunofluorescence and we waited to see a red circle around our bacteria and we saw. We added his-tag because C215 was staining thank to his-tag. During the experiments we used anti-his-tag, after than the substance which will paint… At this step we understood that our bacteria can produce C215 because we saw red circles.
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The second, we did another immunofluorescence experiment too. This experiment’s purpose was to understand that will EpCAM and our C215 bind? Because our experiment which the other immunofluorescence (the OmpA was using there) experiment, we understood that bacteria is producing C215, but we couldn’t understand anything about binding. This time we used cancer cells and we didn’t use bacteria, we used purified C215 to take some information about binding. We put our purified proteins in well-plates with cancer cells. We were expecting to see red color circle around cancer cells and seeing cancer cells’ nucleus blue. After measurements, we saw that the results of the experiment were the correct conclusions.
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Immunofluorescence C215
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In our project we need that our anti-EpCAM active domain c215 bind the membrane of cancer cells. So we decided to make immunofluorescence experiment for tested that our c215 is binding or not? The little red shining cells are our results and show that our c215 is working. With this results we saw that our nanofactory will probably bind to our cancer cells successfully.
  
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This experience page is provided so that any user may enter their experience using this part.<BR>Please enter
 
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how you used this part and how it worked out.
 
  
 
===Applications of BBa_K1202100===
 
===Applications of BBa_K1202100===

Latest revision as of 08:18, 8 October 2013

Firstly we wanted to test that can our bacteria produce C215 (Anti-EpCAM). To test this, we did Immunofluorescence experiments. We put OmpA (a signal peptide which send proteins to membrane) signal peptide sequence and his-tag sequence before C215 protein sequence in our one part. And then we did immunofluorescence and we waited to see a red circle around our bacteria and we saw. We added his-tag because C215 was staining thank to his-tag. During the experiments we used anti-his-tag, after than the substance which will paint… At this step we understood that our bacteria can produce C215 because we saw red circles.

The second, we did another immunofluorescence experiment too. This experiment’s purpose was to understand that will EpCAM and our C215 bind? Because our experiment which the other immunofluorescence (the OmpA was using there) experiment, we understood that bacteria is producing C215, but we couldn’t understand anything about binding. This time we used cancer cells and we didn’t use bacteria, we used purified C215 to take some information about binding. We put our purified proteins in well-plates with cancer cells. We were expecting to see red color circle around cancer cells and seeing cancer cells’ nucleus blue. After measurements, we saw that the results of the experiment were the correct conclusions.

Immunofluorescence C215 In our project we need that our anti-EpCAM active domain c215 bind the membrane of cancer cells. So we decided to make immunofluorescence experiment for tested that our c215 is binding or not? The little red shining cells are our results and show that our c215 is working. With this results we saw that our nanofactory will probably bind to our cancer cells successfully.


Applications of BBa_K1202100

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