Difference between revisions of "Part:BBa K404111:Design"
(→Design Notes) |
|||
Line 1: | Line 1: | ||
− | |||
__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K404111 short</partinfo> | <partinfo>BBa_K404111 short</partinfo> | ||
Line 7: | Line 6: | ||
===Design Notes=== | ===Design Notes=== | ||
− | + | The <b>iGEM team Freiburg_Bioware 2010</b> designed the <b>mGMK</b> in the <b>RFC25 standard</b> and cloned it into the pSB1C3 iGEM standard plasmid. There are now iGEM restriction sites within the sequence. | |
− | + | ||
− | + | ||
===Source=== | ===Source=== |
Revision as of 21:55, 22 October 2010
Mouse guanylate kinase (mGMK)
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 45
Design Notes
The iGEM team Freiburg_Bioware 2010 designed the mGMK in the RFC25 standard and cloned it into the pSB1C3 iGEM standard plasmid. There are now iGEM restriction sites within the sequence.
Source
x