The principle
- 1st step: Isolation of genomic DNA from bodily fluids, tissue or cells.
- 2nd step: Multiplex PCR amplification of specific DNA sequences and simultaneous biotin-labelling.
- 3rd step: Precise selective hybridization of specific sequences onto StripAssay®.
- 4th step: Easy and clear detection and identification of hybridized sequences carrying the variants of interest via streptavidin-conjugated alkaline phosphatase.
- 5th step: Optional automated interpretation of results available.