Difference between revisions of "Part:BBa K243017"

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This part is the counter part to [https://parts.igem.org/wiki/index.php?title=Part:BBa_K243010 BBa_K243010],it inhabits the active cutting site of our universal endonuclease.
 
This part is the counter part to [https://parts.igem.org/wiki/index.php?title=Part:BBa_K243010 BBa_K243010],it inhabits the active cutting site of our universal endonuclease.
We prefer this part because it has an other combiantion of basic parts than BBa_K243010, that allows us another way of purification and linkage to the labeled oligos, which were hybridized with the target DNA.[explication]  
+
We prefer this part because it has an other combiantion of basic parts than His-FluA-Split-Fok_i, that allows us another way of purification and linkage to the labeled oligos, which were hybridized with the target DNA.[explication]  
 
The purification is made with a Streptavidin column.  
 
The purification is made with a Streptavidin column.  
  

Revision as of 18:53, 20 October 2009

Strep-DigA-Split Linker-Fok_a

This part is the counter part to BBa_K243010,it inhabits the active cutting site of our universal endonuclease. We prefer this part because it has an other combiantion of basic parts than His-FluA-Split-Fok_i, that allows us another way of purification and linkage to the labeled oligos, which were hybridized with the target DNA.[explication] The purification is made with a Streptavidin column.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 278
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 1132