Difference between revisions of "Part:BBa K802004"
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== Characterization == | == Characterization == | ||
+ | ===Transformation yield === | ||
+ | <p> In the NM522 E.coli strain the average yield was 3,3XE06 cells/µg.The transformed cells were selected on LB media supplemented with Ampicillin at a concentration of 100µg/mL.</p> | ||
+ | <p> In the BS168 B.subtilis strain the maximum yield was 70 cells/µg. The transformed cells were selected on LB media supplemented with Erythromycin at a concentration of 15µg/mL. </p> | ||
+ | ===Antibiotic resistance=== | ||
+ | ===Sequencing of the modified regions === | ||
<!-- Uncomment this to enable Functional Parameter display | <!-- Uncomment this to enable Functional Parameter display | ||
===Functional Parameters=== | ===Functional Parameters=== | ||
<partinfo>BBa_K802004 parameters</partinfo> | <partinfo>BBa_K802004 parameters</partinfo> | ||
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Revision as of 01:28, 24 September 2012
Shuttle vector for E. coli and B. subtilis
The shuttle vector is Ampicillin resistant in E. coli and Erythromycin resistant in B. subtilis. It is a high plasmid copy number in both B. subtilis and E.coli.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal prefix found in sequence at 6506
Illegal suffix found in sequence at 1 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 6506
Illegal NheI site found at 3377
Illegal SpeI site found at 2
Illegal PstI site found at 16
Illegal NotI site found at 9
Illegal NotI site found at 6512 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 6506
- 23INCOMPATIBLE WITH RFC[23]Illegal prefix found in sequence at 6506
Illegal suffix found in sequence at 2 - 25INCOMPATIBLE WITH RFC[25]Illegal prefix found in sequence at 6506
Illegal XbaI site found at 6521
Illegal SpeI site found at 2
Illegal PstI site found at 16 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 3203
Illegal BsaI.rc site found at 5190
Characterization
Transformation yield
In the NM522 E.coli strain the average yield was 3,3XE06 cells/µg.The transformed cells were selected on LB media supplemented with Ampicillin at a concentration of 100µg/mL.
In the BS168 B.subtilis strain the maximum yield was 70 cells/µg. The transformed cells were selected on LB media supplemented with Erythromycin at a concentration of 15µg/mL.