Difference between revisions of "Part:BBa K2586002:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | + | This part was amplified from ''Bacillus subtilis'' genomic DNA and ligated into the ''EcoRI'' and ''PstI'' digested '''pSB1C3''' backbone. | |
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===Source=== | ===Source=== | ||
− | + | This basic part consists of parts derived from PCR amplification of wild type ''B. subtilis'' chromosomal DNA (strain ''B. subtilis'' 168; Laboratory collection AG Stülke, Department for General Microbiology, University Göttingen). | |
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===References=== | ===References=== |
Latest revision as of 11:00, 10 September 2018
GltP: glutamate and glyphosate uptake transporter in Bacillus subtilis
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 1074
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 709
Design Notes
This part was amplified from Bacillus subtilis genomic DNA and ligated into the EcoRI and PstI digested pSB1C3 backbone.
Source
This basic part consists of parts derived from PCR amplification of wild type B. subtilis chromosomal DNA (strain B. subtilis 168; Laboratory collection AG Stülke, Department for General Microbiology, University Göttingen).