Team:Bologna/Parts

From 2008.igem.org

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The table below shows all the intermediates that we have obtained to build up our final device. For each part you can find:  
The table below shows all the intermediates that we have obtained to build up our final device. For each part you can find:  
-
-in the first column the link to the Registry;  
+
-in the second column the link to the Registry;  
-
-in the second column the components for each part;  
+
-in the third column the components for each part;  
-
-in the third column the plasmid the part has been cloned in;  
+
-in the fourth column the plasmid the part has been cloned in;  
-
-in the fourth the insert length after double digestion with Xba1/Pst1 enzymes linked to the electrophoresis gel run;  
+
-in the fifth the insert length after double digestion with Xba1/Pst1 enzymes linked to the electrophoresis gel run;  
-
-in the fifth column cell vitality after transformation;  
+
-in the sixth column cell vitality after transformation;  
-
-in the sixth column fluo data for each part.  
+
-in the seventh column fluo data for each part.;

Revision as of 10:51, 2 October 2008

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HOME THE PROJECT THE TEAM PARTS SUBMITTED TO THE REGISTRY MODELING NOTEBOOK


Intermediates

The table below shows all the intermediates that we have obtained to build up our final device. For each part you can find:

-in the second column the link to the Registry;

-in the third column the components for each part;

-in the fourth column the plasmid the part has been cloned in;

-in the fifth the insert length after double digestion with Xba1/Pst1 enzymes linked to the electrophoresis gel run;

-in the sixth column cell vitality after transformation;

-in the seventh column fluo data for each part.;


Igem Code Fragment Plasmid Length (bp) Vitality Fluo
1 2 3 4 5 6 7
2
3
4
5