Update wiki/pages/engineering.html

wiki/pages/engineering.html

@@ -178,6 +178,7 @@ The engineering success since when we compare the result is more significant whe
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+
 <h2>Testing TurboID-AIP toxicity to human cells</h2>
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     <b>Purpose:</b><br><br>
@@ -215,14 +216,14 @@ We divided <i>S. aureus</i> into two groups. One is the control group with lysat
 
 
 <b>Result:</b><br><br>
-It is presented that in figure 1, 3, 5, the enterotoxin damages the epithelial cells. In figure 2, 4, 6, the apoptosis rate of cells declined indicating that the damage of enterotoxin decreased. Thus, we can conclude that our project can successfully block the production of enterotoxin in <i>S. aureus</i>.<br><br>
+It is presented that in figure 3, 5, 7, the enterotoxin damages the epithelial cells. In figure 4, 6, 8, the apoptosis rate of cells declined indicating that the damage of enterotoxin decreased. Thus, we can conclude that our project can successfully block the production of enterotoxin in <i>S. aureus</i>.<br><br>
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 <img src="https://static.igem.wiki/teams/4329/wiki/engineering-success/new-16.jpg
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-Fig.1 Analysis of epithelial cell of subject 1 with <i>S. aureus</i> lysate from (A) to (C); (A) size of the cells. (B) width of cells. It eliminates the duplicates which are useless to the Analysis. (C) The apoptosis rate of cells.
+Fig.3 Analysis of epithelial cell of subject 1 with <i>S. aureus</i> lysate from (A) to (C); <br>(A) size of the cells. (B) width of cells. It eliminates the duplicates which are useless to the Analysis. (C) The apoptosis rate of cells.
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@@ -230,7 +231,7 @@ Fig.1 Analysis of epithelial cell of subject 1 with <i>S. aureus</i> lysate from
 <img src="https://static.igem.wiki/teams/4329/wiki/engineering-success/new-26.jpg
 " alt="" width="75%">
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-Fig.2 Analysis of epithelial cell of subject 1 with biotin labeled <i>S. aureus</i> lysate from (A) to (C); (A) size of the cells. (B) width of cells. It eliminates the duplicates which are useless to the Analysis. (C) The apoptosis rate of cells.
+Fig.4 Analysis of epithelial cell of subject 1 with biotin labeled <i>S. aureus</i> lysate from (A) to (C);<br> (A) size of the cells. (B) width of cells. It eliminates the duplicates which are useless to the Analysis. (C) The apoptosis rate of cells.
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@@ -238,7 +239,7 @@ Fig.2 Analysis of epithelial cell of subject 1 with biotin labeled <i>S. aureus<
 <img src="https://static.igem.wiki/teams/4329/wiki/engineering-success/new-36.jpg
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-Fig.3 Analysis of epithelial cell of subject 2 with <i>S. aureus</i> lysate from (A) to (C); (A) size of the cells. (B) width of cells. It eliminates the duplicates which are useless to the Analysis. (C) The apoptosis rate of cells.
+Fig.5 Analysis of epithelial cell of subject 2 with <i>S. aureus</i> lysate from (A) to (C); <br>(A) size of the cells. (B) width of cells. It eliminates the duplicates which are useless to the Analysis. (C) The apoptosis rate of cells.
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@@ -247,7 +248,7 @@ Fig.3 Analysis of epithelial cell of subject 2 with <i>S. aureus</i> lysate from
 <img src="https://static.igem.wiki/teams/4329/wiki/engineering-success/new-46.jpg
 " alt="" width="75%">
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-Fig.4 Analysis of epithelial cell of subject 2 with biotin labeled <i>S. aureus</i> lysate from (A) to (C); (A) size of the cells. (B) width of cells. It eliminates the duplicates which are useless to the Analysis. (C) The apoptosis rate of cells.
+Fig.6 Analysis of epithelial cell of subject 2 with biotin labeled <i>S. aureus</i> lysate from (A) to (C); <br>(A) size of the cells. (B) width of cells. It eliminates the duplicates which are useless to the Analysis. (C) The apoptosis rate of cells.
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@@ -255,7 +256,7 @@ Fig.4 Analysis of epithelial cell of subject 2 with biotin labeled <i>S. aureus<
 <img src="https://static.igem.wiki/teams/4329/wiki/engineering-success/new-56.jpg
 " alt="" width="75%">
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-Fig.5 Analysis of epithelial cell of subject 3 with <i>S. aureus</i> lysate from (A) to (C); (A) size of the cells. (B) width of cells. It eliminates the duplicates which are useless to the Analysis. (C) The apoptosis rate of cells.
+Fig.7 Analysis of epithelial cell of subject 3 with <i>S. aureus</i> lysate from (A) to (C);<br> (A) size of the cells. (B) width of cells. It eliminates the duplicates which are useless to the Analysis. (C) The apoptosis rate of cells.
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@@ -263,11 +264,10 @@ Fig.5 Analysis of epithelial cell of subject 3 with <i>S. aureus</i> lysate from
 <img src="https://static.igem.wiki/teams/4329/wiki/engineering-success/new-66.jpg
 " alt="" width="75%">
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-Fig.6 Analysis of epithelial cell of subject 3 with biotin labeled <i>S. aureus</i> lysate from (A) to (C); (A) size of the cells. (B) width of cells. It eliminates the duplicates which are useless to the Analysis. (C) The apoptosis rate of cells
+Fig.8 Analysis of epithelial cell of subject 3 with biotin labeled <i>S. aureus</i> lysate from (A) to (C); <br>(A) size of the cells. (B) width of cells. It eliminates the duplicates which are useless to the Analysis. (C) The apoptosis rate of cells
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-
 <h2>Protecting food from <i>S. aureus</i> contamination</h2>
 
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@@ -307,7 +307,7 @@ DNA electrophoresis：200V run for 30-60min, solution:5 ul ER staining for 100 m
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 <img src="https://static.igem.wiki/teams/4329/wiki/engineering-success/fig10.png" alt="" width="70%">
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-    Fig.10 DNA electrophoresis of control groups and experimental groups from PCR
+    Fig.9 DNA electrophoresis of control groups and experimental groups from PCR
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