Difference between revisions of "Part:BBa K292004:Design"
Line 1: | Line 1: | ||
− | |||
__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K292004 short</partinfo> | <partinfo>BBa_K292004 short</partinfo> | ||
Line 9: | Line 8: | ||
When we design the bio-brick it was impossible to obtain a functional bio-brick by using the plasmid SB1AK3. But it's worked with a pSB1A1. | When we design the bio-brick it was impossible to obtain a functional bio-brick by using the plasmid SB1AK3. But it's worked with a pSB1A1. | ||
− | + | [[Part:BBa_P1003|BBa_P1003]] is an kanamycin antibiotic resistance cassette. Several silent mutations have been introduced to eliminate useful restriction sites and rare codons. However, we inadvertently introduced a new BsmBI recognition site in BBa_P1003 (kanamycin antibiotic resistance marker) during the course of codon shuffling. <br> | |
===Source=== | ===Source=== |
Revision as of 21:17, 21 October 2009
Double terminator + Kanamycin resistance cassette + Double ter
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
When we design the bio-brick it was impossible to obtain a functional bio-brick by using the plasmid SB1AK3. But it's worked with a pSB1A1.
BBa_P1003 is an kanamycin antibiotic resistance cassette. Several silent mutations have been introduced to eliminate useful restriction sites and rare codons. However, we inadvertently introduced a new BsmBI recognition site in BBa_P1003 (kanamycin antibiotic resistance marker) during the course of codon shuffling.
Source
Part:BBa_B0014, Designed by Reshma Shetty Group: Registry (2003-07-16) Part:BBa_P1003, Designed by Reshma Shetty Group: Knight Lab, MIT (2006-01-23)