Since Mendel studied the basic principle of genetics in peas, the use of genetic-driven decision in plant breeding has been growing constantly. Nowadays, genetic markers are largely brought into play to avoid the need of phenotyping. The so-called marker-assisted selection (MAS) applies diagnostic markers to forecast the phenotype and optimize the selection of new crops. Since the comprehensive sequencing of plants, such as maize, has become readily available, single nucleotide polymorphisms (SNPs) have been widely used in MAS.

However, the extraction of DNA from plants is generally difficult and time-consuming, due to the presence of a tough cell wall and several contaminants, such as polysaccharides, polyphenols, tannins, and alkaloids. Overcoming this issue in DNA extraction will set the springboard for more efficient plant molecular breeding.

In this application note, we show a novel workflow combining different technologies to reduce time, plastic consumption, and costs of plant DNA extraction, as well as increase the analysis throughput. The workflow suggested here includes:

  • MicroGEM’s phytoGEM chemistry for rapid temperature-driven extraction (TDE) of DNA from seeds, leaves, and roots of rapeseed plants (Brassica Napus);
  • Hydrocycler (LGC) to run high-throughput TDE and Kompetitive Allele Specific PCR for the genotyping.

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Produces double-stranded DNA suitable for PCR and qPCR.

Each kit contains PDQeX prepGEM, Histosolv, enhancer, GREEN+ buffer, and extractor tubes.

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