Difference between revisions of "Part:BBa K108014:Design"
Angel6767Q (Talk | contribs) (→References) |
|||
(One intermediate revision by the same user not shown) | |||
Line 1: | Line 1: | ||
− | |||
__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K108014 short</partinfo> | <partinfo>BBa_K108014 short</partinfo> | ||
Line 13: | Line 12: | ||
===Source=== | ===Source=== | ||
− | Alcaligenes eutrophus H16 genome | + | PR was cloned from Alcaligenes eutrophus H16 genome (reference 1 and 2). |
===References=== | ===References=== | ||
+ | |||
+ | 1. Regulation of phasin expression and polyhydroxyalkanoate (PHA) granule formation | ||
+ | in Ralstonia eutropha H16. Microbiology. 2002, 148:2413–2426. | ||
+ | |||
+ | 2. NCBI. |
Latest revision as of 06:07, 25 October 2008
PR
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 136
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
PCR using primers with biobrick prefix and surfix, cloned into pSB1AC3, and then eliminate Pst1 using site-directed mutation.
Source
PR was cloned from Alcaligenes eutrophus H16 genome (reference 1 and 2).
References
1. Regulation of phasin expression and polyhydroxyalkanoate (PHA) granule formation in Ralstonia eutropha H16. Microbiology. 2002, 148:2413–2426.
2. NCBI.