Difference between revisions of "Part:BBa K1943018:Design"
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===Source=== | ===Source=== | ||
| − | + | The plasmid was from our instructor, Huangwei's lab. And we design primers to copy down by PCR. | |
===References=== | ===References=== | ||
| + | #[[About_Assembly|Parts Registry Assembly Help]] | ||
| + | #[[Help:Protocols/Transformation|Parts Registry Transformation Guideline]] | ||
Latest revision as of 03:29, 22 October 2016
T2A+Bleo
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 330
Illegal NgoMIV site found at 391 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
This year we use mammalian cells as carriers. So in our plasmids, there are several kinds of anti-antibiotics genes which are used for screening. Usually, we will not use anti-antibiotics genes individually. We often use them together with some core protein such as GECO. However, it is monocistronic in the eukaryotic cells. There is a DNA sequence called 2A which connects two coding sequence and then both two call be expressed by the same promoter. We design primers and do PCR of this anti-antibiotics genes coding sequence together with 2A sequence and ligate it to pSB1C3 backbone.
Source
The plasmid was from our instructor, Huangwei's lab. And we design primers to copy down by PCR.