With less than 10 minutes of set-up and no further operator intervention, LinkSēq™ uses state of the art real-time PCR detection to provide complete molecular genotyping results in approximately 90 minutes.
The LinkSēq™ methodology is based on allele specific PCR similar to current SSP methods; however, unlike SSP, LinkSēq utilizes SYBR® Green to identify the presence or absence of alleles.
LinkSēq™ uses SYBR® Green, a non-toxic alternative to ethidium bromide, to determine the presence or absence of specific alleles. When bound to double stranded DNA, SYBR Green fluoresces. A Real-Time PCR instrument is used to take fluorescent readings of each well at different temperatures. As the temperature increases, the DNA will “melt” and the fluorescence will decrease. Graphing the melt-curve makes visualizing the results easy, and allows the software to easily identify if an allele is present or absent.
SureTyper™ is the software platform used in combination with LinkSēq™ Real-Time PCR kits for automating data interpretation and simplifying genotype reporting.
LinkSēq is a rapid genotyping method with a simple workflow that avoids post-amplification contamination. Given the ease of use, rapid turn around times, and increased laboratory productivity, LinkSēq offers an attractive improvement over current SSP and SSOP typing methods.