Archer Comprehensive NGS assays
Inherited Disease Assays


Archer® Variantplex® kits for inherited diseases are highly customizable assays that deliver comprehensive coverage of target exons for genes associated with breast cancer risk (BRCA 1/2 & PALB2) and cystic fibrosis (CFTR).

 

The Archer advantage



Key features of germline assays

Safeguard against allelic dropout
Dual, independent coverage across target regions ensures that coverage is retained when one primer drops out due to primer-blocking SNVs
Superior coverage
AMP chemistry provies complete, strand-specific and bi-directional coverage of target exons to maximize variant detection
Single-day lyophilized workflow
Easy-to-handle lyophilized reagents and a simple workflow mean libraries can be made in a single day
Customization
Create from scratch or modify either kit below to match the pace of discovery

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Catalog kits: on the shelf and ready for delivery

FOR RESEARCH USE ONLY. Not for use in diagnostic procedures.




How to contact us

Address

2477 55th Street, Suite 202

Boulder, CO 80301

Phone

Phone: (877) 771 1093

Phone: (303) 357 9001

All content © 2018 ArcherDX, Inc.

For Research Use Only. Not for use in diagnostic procedures. For Research Use Only. Not for use in diagnostic procedures.