Rapid, Simultaneous Detection of 40 Mutations Within the LDLR, ApoB and PCSK9 Genes

28 November 2014

This video introduces the Familial Hypercholesterolemia Arrays from Randox, which allow simultaneous detection of 40 FH-causing mutations within three common genes implicated in FH. Samples can be assessed in small batches in a turnaround time of less than three hours and only 20ng of genomic DNA per array is required.