● Simple and fast: Ultra-pure genomic DNA can be obtained by running TGuide S16 for 60 minutes.

● Widely applicable: It is suitable for a variety of plant tissues, especially polysaccharide or polyphenol-rich plants.

● Safe and non-toxic: No toxic organic reagents such as phenol/chloroform.

● High purity: The obtained DNA has high purity and can be directly used for chip detection, high-throughput sequencing and other experiments.

This product adopts magnetic beads and a unique buffer system to isolate and purify high-quality genomic DNA from various plant tissues. The uniquely embedded magnetic beads have a strong affinity for nucleic acid under certain conditions. When the conditions are changed, the magnetic beads can release the absorbed nucleic acid to rapidly separate and purify the nucleic acid.

It can be used to perfectly fit with TGuide S16 Nucleic Acid Extractor. Through absorption, transfer and release of magnetic beads by the special magnetic bar, magnetic beads and nucleic acid can be transferred to improve the degree of automation. The whole process is safe and convenient, and the extracted genomic DNA fragments are large, with high purity and reliable quality.

The DNA purified by this kit is suitable for a range of common downstream applications including digestion, PCR, library construction, Southern hybridization, and other experiments.

For purification of genomic DNA from various plant Tissues

All components of the kit can be stored in dry conditions at room temperature (15~30°C) for 12 months. If the solution precipitates, it can be preheated in a water bath at 37°C for 10 min before use to dissolve the precipitation, without affecting the effect.

● To use the TGuide Smart Magnetic Plant DNA Kit, you must have the TGuide Smart Magnetic Plant DNA (program no. DP607) installed on the TGuide S16/S32 pro Nucleic Acid Extractor.

● Repeated freezing and thawing samples should be avoided, otherwise the extracted DNA fragments will be small and the total yield will decrease.

● If there is precipitation in the buffer GPS, it can be dissolved in a 37°C water bath and used after shaking well.

The size of the obtained genomic DNA fragment is affected by the sample storage time and shear force during operation. The concentration and purity of the obtained DNA fragments can be detected by agarose gel electrophoresis and UV spectrophotometer. Ideally, the DNA should absorb at most at OD260, where an OD260 value of 1 corresponds to approximately 50 μg/ml double strand DNA and 40 μg/ml single strand DNA. The OD260/OD280 ratio should be 1.7~1.9.