SURVEYOR® Mutation Detection Kit for Standard Gel Electrophoresis
SURVEYOR Mutation Detection Kits provide a simple, accurate and cost-effective means to scan DNA fragments for mutations with unmatched sensitivity and specificity. The SURVEYOR Mutation Detection Kit for Standard Gel Electrophoresis has been designed to cleave unlabeled DNA fragments at mismatched sites for subsequent analysis by agarose gel electrophoresis or polyacrylamide gel electrophoresis (PAGE). DNA 200 to 4,000 bp lo…
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Fast and easy way to check SNPs.
Gene editing
My job involves working on CRISPR Cas9 base editor and before sending my samples for next-generation sequencing, I need to check them in an easy and quick way. This kit is very sensitive to even a single mismatch and can be used to get a result in 1 or 2 hrs with a simple agarose gel. Since it has its own positive control I can make sure of the accuracy
Review Date: 12 Jun 2020 | Transgenomic Inc.
Genomic Editing
This is a very easy-to-use, fail-proof kit, great to check any indels in any gene sequences.
Review Date: 5 Aug 2014 | Transgenomic Inc.
SURVEYOR Mutation Detection Kits provide a simple, accurate and cost-effective means to scan DNA fragments for mutations with unmatched sensitivity and specificity.
The SURVEYOR Mutation Detection Kit for Standard Gel Electrophoresis has been designed to cleave unlabeled DNA fragments at mismatched sites for subsequent analysis by agarose gel electrophoresis or polyacrylamide gel electrophoresis (PAGE). DNA 200 to 4,000 bp long can be analyzed using manual agarose gel electrophoresis while smaller fragments (<1,000 bp) can be analyzed using manual polyacrylamide gel electrophoresis (PAGE).
Benefits:
- Determines mutation loci
- Saves time and money
– Streamlines DNA sequencing
– Decreases sequencing backlog and analysis time
– Validates sequencing results and analysis
– Decreases chromatogram analysis by 90% - No post-PCR or post-reaction clean-up
- High throughput sensitivity and specificity
Applications:
- Somatic, germ-line and mitochondrial mutations
- Insertions, deletions, substitutions and SNPs
- Low-copy mutations and pooled DNA samples
