Difference between revisions of "Part:BBa K5071021"
Line 9: | Line 9: | ||
<partinfo>BBa_K5071021 SequenceAndFeatures</partinfo> | <partinfo>BBa_K5071021 SequenceAndFeatures</partinfo> | ||
− | + | ||
<html lang="en"> | <html lang="en"> | ||
<head> | <head> |
Latest revision as of 06:24, 30 September 2024
pETDuet-1 backbone
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Plasmid lacks a prefix.
Plasmid lacks a suffix. - 12INCOMPATIBLE WITH RFC[12]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal NotI site found at 149 - 21INCOMPATIBLE WITH RFC[21]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal BglII site found at 305
Illegal BamHI site found at 106
Illegal XhoI site found at 354 - 23INCOMPATIBLE WITH RFC[23]Plasmid lacks a prefix.
Plasmid lacks a suffix. - 25INCOMPATIBLE WITH RFC[25]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal NgoMIV site found at 324
Illegal NgoMIV site found at 671
Illegal NgoMIV site found at 5348 - 1000INCOMPATIBLE WITH RFC[1000]Plasmid lacks a prefix.
Plasmid lacks a suffix.
BBa_K5071021 (pETDuet-1 backbone)
Name
pETDuet-1 backbone
Base Pairs
5178 bp
Origin
Escherichia coli
Usage and Biology
The pETDuet-1 backbone is a plasmid vector obtained by linearizing the plasmid pETD, and we used this vector for the connection of the target genes.
Cultivation
The pETDuet-1 backbone is a plasmid vector obtained by linearizing the plasmid pETD, with a length of 5178 bp. Fig 1. shows a band consistent with the target size, indicating that the target gene was successfully amplified. After agarose gel electrophoresis and gel recovery, homologous recombination was used to obtain the recombinant plasmid.