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

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.