KASP SNP Genotyping Reagents by LGC Biosearch Technologies

"Have been using this assay for genotyping. Reproducible results, time-saving assay"

"The KASP SNP genotyping reagents are very easy to use, reliable, stable and comes with good "how to use" manuals. The only thing to complain about is the delivery time of reagents, we often need our ordered products quite fast, but your fast turnaround time is two weeks and most often it even takes a few days more.."

"Easy to use and cost-effective product Give reproducible results of good quality. Very satisfied since using it."

"We use KBD assays, ordering KASP markers for plant genotpying for the aim of genetic mapping. Very easy and efficient syste, only a qPCR machine and a bit of a plactiware are required. Would use more the KBD assays, if it would be a bit cheaper and a bit quicker for marker ordering, but very glad of the service overall. Maybe a bar-coded system would help to order big batch of oligos in advance, then you just have to submit the sequence of interest."

"It is very cheap, easy to manage and to find false positives. It was a surprise to work with them."

"The KASPar technique has been a great acquisition in our laboratory. We have easyly genotyped hundreds of samples with many different SNPs."

"Super fast method for analyzing large numbers of samples. This product is helpful for analyzing segregating population on a large scale. For example, searching for the EMS mutated candidate gene responsible for the phenotype in segregating population after outcross. Only 3 components (DNA of interest, KASP reagent and KASP assay) required, therefore very easily done in 96 well plate. Easy to analyze the results. Mostly no false positive observed. One of best, quick and easy assays in my PhD work."

"The method for distinguishing two different alleles and the combination is very easy to use, less expensive for genotyping compared to sequencing whole sequences. However the cost for primer designing is still quite expensive. It is a very good breakthrough to know genetic occurrences at nucleotide level."