840:153g:Projects/project20/2011/10/13

From OpenWetWare

< 840:153g:Projects | project20 | 2011 | 10(Difference between revisions)
Jump to: navigation, search
(Autocreate 2011/10/13 Entry for 840:153g:Projects/project20)
Current revision (17:58, 18 October 2011) (view source)
(Entry title)
 
Line 6: Line 6:
| colspan="2"|
| colspan="2"|
<!-- ##### DO NOT edit above this line unless you know what you are doing. ##### -->
<!-- ##### DO NOT edit above this line unless you know what you are doing. ##### -->
-
==Entry title==
+
==electrophoresis for pcr production and transformation agian for our promotors==
-
* Insert content here...
+
* after the gel, we found that the most briht bands' BP were less than waht we expected.  
-
 
+
* in the posion where our expected band should be, we had weak band. so, we need pcr again by using diff tm to see if we can get more in that posiotion.  
-
 
+
* transform 3 promoters into e.coli, see if we can get a useful promoter for recombine( forgot +control this time)
 +
  Part:BBa_K091112  Part:BBa_K206001  Part:BBa_I0500
<!-- ##### DO NOT edit below this line unless you know what you are doing. ##### -->
<!-- ##### DO NOT edit below this line unless you know what you are doing. ##### -->
|}
|}

Current revision

Project name Main project page
Previous entry      Next entry

electrophoresis for pcr production and transformation agian for our promotors

  • after the gel, we found that the most briht bands' BP were less than waht we expected.
  • in the posion where our expected band should be, we had weak band. so, we need pcr again by using diff tm to see if we can get more in that posiotion.
  • transform 3 promoters into e.coli, see if we can get a useful promoter for recombine( forgot +control this time)
  Part:BBa_K091112   Part:BBa_K206001   Part:BBa_I0500 
Personal tools