Difference between revisions of "Part:BBa K4158010:Design"
(→Design Notes) |
(→Design Notes) |
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1. Prepare pACYC184 cloning vector and this part as BioBrick. | 1. Prepare pACYC184 cloning vector and this part as BioBrick. | ||
− | 2. Restriction and insertion cloning with pACYC184 and this BioBrick productions and restriction enzymes HindIII and BamHI. | + | 2. Restriction and insertion cloning with pACYC184 and this BioBrick productions and restriction enzymes HindIII and BamHI. |
===Source=== | ===Source=== |
Latest revision as of 02:47, 24 September 2022
Psrtf1-GFP
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 13
Illegal NheI site found at 36 - 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 826
Illegal XhoI site found at 529 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
If you want to get the same plasmid that we experimented with, construct the plasmid along the way below.
1. Prepare pACYC184 cloning vector and this part as BioBrick.
2. Restriction and insertion cloning with pACYC184 and this BioBrick productions and restriction enzymes HindIII and BamHI.
Source
test