Overview
BTSeq™ Full Plasmid Sequencing Service allows for the most
effective analysis of the full-length sequencing of plasmids
with shorter TAT and lower costs than Sanger sequencing.
synthetic biology, and various other applications.
Features &
Benefits
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- Fast TAT, No Need of Primer Walking
- NGS-based result, within 24 hours after sample arrival
- No need of repetitive primer synthesis and Sanger sequencing cycles
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- NGS-based, High Sequencing Accuracy
- NGS technology-based BTSeq™ Full Plasmid Sequencing
provides accurate sequencing results. - Digitized sequencing results
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- Wide range of DNA size
- BTSeq™ Full Plasmid Sequencing support up to 20kb large
length sequencing, enabling the sequencing of large insert
and insert with plasmid vector.
Performance
Comparison IGV data between normal and mutated vectors
Compared to Sanger sequencing, which is limited to 1000 bp sequencing,
BTSeq™ Full Plasmid Sequencing Service can accurately sequence
up to 20 kb with all types of mutations including indel.
By Celemics’ user-friendly sequencing report, customers can easily compare
the sequence differences with their own vector and insert.
Application of
BTSeq™
Applications of BTSeq™ Full Plasmid Sequencing
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Gene expression profiling
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Detection of structural variations of gene
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Validation of results from total RNA sequencing
- Compared to Sanger sequencing, which is limited to 1000 bp sequencing,
BTSeq™ Full Plasmid Sequencing Service can accurately sequence up to 20 kb with all types of mutations including indel. - By Celemics’ user-friendly sequencing report, customers can easily compare the sequence differences with their own vector and insert.
Applications
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Vector engineering
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Plasmid sequence validation