Difference between revisions of "Part:BBa K5071022"
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<partinfo>BBa_K5071022 short</partinfo> | <partinfo>BBa_K5071022 short</partinfo> | ||
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<partinfo>BBa_K5071022 SequenceAndFeatures</partinfo> | <partinfo>BBa_K5071022 SequenceAndFeatures</partinfo> | ||
+ | <!DOCTYPE html> | ||
+ | <html lang="en"> | ||
+ | <head> | ||
+ | <meta charset="UTF-8"> | ||
+ | <meta name="viewport" content="width=device-width, initial-scale=1.0"> | ||
+ | <title>BBa_K5071022 (pRSFDuet-1 backbone)</title> | ||
+ | <style> | ||
+ | img { | ||
+ | max-width: 80%; | ||
+ | height: auto; | ||
+ | } | ||
+ | .caption { | ||
+ | text-align: center; | ||
+ | font-size: 0.9em; | ||
+ | margin-top: 5px; | ||
+ | margin-bottom: 20px; | ||
+ | } | ||
+ | table { | ||
+ | width: 100%; | ||
+ | border-collapse: collapse; | ||
+ | margin-top: 20px; | ||
+ | margin-bottom: 20px; | ||
+ | } | ||
+ | th, td { | ||
+ | border: 1px solid #ddd; | ||
+ | padding: 8px; | ||
+ | text-align: center; | ||
+ | } | ||
+ | th { | ||
+ | background-color: #f2f2f2; | ||
+ | } | ||
+ | </style> | ||
+ | </head> | ||
+ | <body> | ||
+ | <h2>BBa_K5071022 (pRSFDuet-1 backbone)</h2> | ||
− | < | + | <h3>Name</h3> |
− | === | + | <p>pRSFDuet-1 backbone</p> |
− | < | + | |
− | < | + | <h3>Base Pairs</h3> |
+ | <p>3587 bp</p> | ||
+ | |||
+ | <h3>Origin</h3> | ||
+ | <p>Escherichia coli</p> | ||
+ | |||
+ | <h3>Usage and Biology</h3> | ||
+ | <p> | ||
+ | The pRSFDuet-1 backbone is a plasmid vector obtained by linearizing the plasmid pRSFD, and we used this vector for the connection of the target genes. | ||
+ | </p> | ||
+ | |||
+ | <h3>Cultivation</h3> | ||
+ | <p> | ||
+ | The pRSFDuet-1 backbone is a plasmid vector obtained by linearizing the plasmid pRSFD, with a length of 3587 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. | ||
+ | </p> | ||
+ | |||
+ | <div style="text-align:center;"> | ||
+ | <img src="https://static.igem.wiki/teams/5071/bba-k5071022/1.jpg" alt="Fig 1. The purpose segment of backbone pRSFDuet-1"> | ||
+ | <div class="caption">Fig 1. The purpose segment of backbone pRSFDuet-1</div> | ||
+ | </div> | ||
+ | |||
+ | </body> | ||
+ | </html> |
Latest revision as of 06:12, 30 September 2024
pRSFDuet-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 AgeI site found at 566 - 1000INCOMPATIBLE WITH RFC[1000]Plasmid lacks a prefix.
Plasmid lacks a suffix.
<!DOCTYPE html>
BBa_K5071022 (pRSFDuet-1 backbone)
Name
pRSFDuet-1 backbone
Base Pairs
3587 bp
Origin
Escherichia coli
Usage and Biology
The pRSFDuet-1 backbone is a plasmid vector obtained by linearizing the plasmid pRSFD, and we used this vector for the connection of the target genes.
Cultivation
The pRSFDuet-1 backbone is a plasmid vector obtained by linearizing the plasmid pRSFD, with a length of 3587 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.