Difference between revisions of "Part:BBa K318030:Design"
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<partinfo>BBa_K318030 short</partinfo> | <partinfo>BBa_K318030 short</partinfo> | ||
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===Design Notes=== | ===Design Notes=== | ||
− | Note | + | Note: |
− | + | *The constitutive promoter is oriented to express whatever gene is downstream of the final hixC site after recombination. | |
− | + | *The SapI site located within the part yields a cut site as shown 5'(A\ATCT)3' on top and 3'(TTAG\A)5' on bottom. | |
+ | *The HindIII site located within the part actually allows for "lock breaking" because inserting a promoter into the part through standard cloning protocols bypasses the "lock" effect. The site was added to more easily recognize different recombinants through restriction digests. | ||
===Source=== | ===Source=== | ||
− | From | + | From synthesis but the same construct can be made with biobricks. |
===References=== | ===References=== |
Latest revision as of 20:24, 27 September 2010
lox66 + rpCons + hixC + lox71 + SapI + T + T + Hin enhancer + HindIII + hixC
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 43
Illegal NheI site found at 66 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 162
Design Notes
Note:
- The constitutive promoter is oriented to express whatever gene is downstream of the final hixC site after recombination.
- The SapI site located within the part yields a cut site as shown 5'(A\ATCT)3' on top and 3'(TTAG\A)5' on bottom.
- The HindIII site located within the part actually allows for "lock breaking" because inserting a promoter into the part through standard cloning protocols bypasses the "lock" effect. The site was added to more easily recognize different recombinants through restriction digests.
Source
From synthesis but the same construct can be made with biobricks.