Difference between revisions of "Part:BBa K5531006"
Line 17: | Line 17: | ||
<style> | <style> | ||
img { | img { | ||
− | max-width: | + | max-width: 60%; /* Adjust this percentage to change size relative to text */ |
height: auto; /* Maintain aspect ratio */ | height: auto; /* Maintain aspect ratio */ | ||
} | } |
Latest revision as of 03:56, 30 September 2024
pET-Dual-N-His-TEV
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 150 - 21INCOMPATIBLE WITH RFC[21]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal BglII site found at 305
Illegal BamHI site found at 119
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 5341 - 1000INCOMPATIBLE WITH RFC[1000]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal BsaI.rc site found at 1256
BBa_K5531006 (pET-Dual-N-His-TEV)
Profile
Name: pET-Dual-N-His-TEV
Base Pairs: 5413 bp
Origin: Escherichia coli; synthesized
Properties: A plasmid for efficient co-expression of two target proteins in Escherichia coli, wherein one of the two target proteins expressed can be His-tagged, and a TEV protease cleavage site follows the His-tag. The plasmid contains two polyclonal sites (MCS), each preceded by a T7 promoter/lac operon and a ribosome binding site (RBS), which can efficiently initiate the expression of the target proteins induced by IPTG.