Confirming genome edits with Sanger sequencing is an important step in determining the efficiency of CRISPR-mediated genome editing. Our CRISPR Sanger sequencing service is designed to verify the successful edit of your region of interest, starting with cells or genomic DNA.
Our Mutation Analysis service includes PCR optimization, amplicon production and purification, and Sanger sequencing for your CRISPR regions of interest. Whether you are confirming that a mutation has occurred or precisely determining the genotype and specific allelic event, leveraging our expertise ensures that your genome editing functions efficiently.
For CRISPR experiments, our experienced scientists can interrogate your specified on-target regions of interest. GENEWIZ can also confirm off-target effects of the RNA-guided Cas9 nuclease1. Simply identify your target regions and let our Sanger experts handle the rest.
1 Nucleic Acids Research (2014) doi: 10.1093/nar/gku402. CRISPR/Cas9 systems have off-target activity with insertions or deletions between target DNA and guide RNA sequences. Lin, Y, et. Al.
High-Throughput Processing: Target regions are amplified using optimized assays; amplicons are purified and sequenced by capillary electrophoresis in our best-in-class facility.