Difference between revisions of "Part:BBa K203117:Design"
(→Source) |
|||
| (One intermediate revision by the same user not shown) | |||
| Line 1: | Line 1: | ||
| − | |||
__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K203117 short</partinfo> | <partinfo>BBa_K203117 short</partinfo> | ||
| Line 7: | Line 6: | ||
===Design Notes=== | ===Design Notes=== | ||
| − | |||
| − | |||
| + | Both parts were PCR amplified out of plasmids to get the BBb-standard restriction sites. They were combinied by BBb standard assembly. | ||
===Source=== | ===Source=== | ||
| − | + | Amplified out of a plasmid. | |
===References=== | ===References=== | ||
Latest revision as of 11:09, 18 October 2009
GFP-polyA
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
Both parts were PCR amplified out of plasmids to get the BBb-standard restriction sites. They were combinied by BBb standard assembly.
Source
Amplified out of a plasmid.