Comprehensive coverage for cystic fibrosis research
Interrogate all 27 exons and key intronic regions in the Cystic Fibrosis Conductance Regulator (CFTR) gene for germline variants, including detection and analysis of variants important for equitable research in diverse populations.
Detect confidently with Archer VARIANTPlex NGS Panels for DNA.
Learn how the VARIANTPlex CFTR v2 panel can identify key genetic alterations for your research.
Request a consultationSpecifications | |
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Targeted genes | CFTR |
Genomic alterations | SNVs, structural variants, ITDs |
Input nucleic acid required* | ≥10 ng |
Recommended number of reads | 100 K |
Hands-on time | <2.5 hours |
Total library prep time | 1.5 days |
Platform compatibility | Illumina® |
Reagent format | Lyophilized or liquid |
Supported sample types | Whole blood |
*Input mass requirements vary depending on type and quality. Unless the tumor cellularity and sample quality are high, 50 ng of FFPE-derived nucleic acid should be considered the minimum recommendation. If input is not limiting, 200 ng is recommended.
Gene | Regions covered |
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CFTR | 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, Select intronic variants |
Customize this NGS panel by adding any of our functionally-tested designs or create a new panel that fits your exact requirements with Assay Marketplace.
Talk with our technical sales team. Learn how the VARIANTPlex CFTR v2 panel can identify key genetic alterations for your research.
Request a consultationRUO23-2271_001