HigherPurity™ Plant DNA Purification Kit

Name: HigherPurity™ Plant DNA Purification Kit
SKU: AN0110
Availability: InStock

HigherPurity™ Plant DNA Purification Kit provides a fast, efficient, and convenient method for isolating high-quality total DNA from a wide variety of plant tissues, including leaves, roots, and seeds.
Using optimized silica membrane technology and chaotropic salts, the kit ensures the removal of polysaccharides, polyphenols, and other inhibitors — producing pure DNA in under 1 hour, ready for PCR, Southern blotting, or RFLP.

HigherPurity™ Plant DNA Purification Kit offers a highly efficient, convenient, and rapid method for purifying total genomic DNA from diverse plant tissues.
The system uses HigherPurity™ silica-binding technology, where DNA selectively binds to a silica membrane in the presence of high concentrations of chaotropic salts, such as guanidinium thiocyanate.

This approach effectively removes common plant-derived contaminants, including polysaccharides, polyphenols, and secondary metabolites, that can inhibit enzymatic reactions.
The purified DNA is of high quality and suitable for all molecular biology applications, including PCR, RFLP, and blotting techniques.

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Price: 159.90 € – 501.90 €

size

50 rxn

100 rxn

250 rxn

SKU: AN0110 Categories: DNA Extraction Kits, DNA & RNA Extraction

Detailed information:

Advantages & Features

High efficiency: yields up to 5–40 µg of total DNA from young leaves..
High purity: removes polysaccharides, polyphenols, and enzyme inhibitors.
Fast and simple: obtain DNA in ~56 minutes with minimal hands-on time.
Versatile: suitable for DNA extraction from various plant species and tissue types.
Mini format: compact and convenient for routine laboratory use.
Ready-to-use DNA: compatible with all downstream applications (PCR, cloning, sequencing).

Specifications

Includes

Includes for 50 rxn:
– 50 DNAprep Spin Columns
– 50 Filter columns
– 100 Collection tubes (2 mL)
– 25 mL BL1 Buffer
– 7.5 mL BL2 Buffer
– 15 mL BL3 Buffer
– 13 mL Wash Buffer 1
– 15 mL Wash Buffer 2
– 10 mL Elution Buffer
– 480 μL RNase A Solution

Download documentation

Datasheet

MSDS

Applications

Purified DNA suitable for all common Molecular Biology applications, such as:

RT-PCR.
Southern blotting.
Restriction Fragment Length Polymorphism (RFLP)
Sequencing and cloning
Genotyping and marker-assisted selection

Tables & Figures

Quality Control

Total DNA is isolated from a 100 mg young leaf sample, quantified with a spectrophotometer and analysed by electrophoresis.

Advice

Storage, Shipping & Guarantee

Shipped in: Ambient Temperature.
Storage: Room Temperature (15–25 °C). Store RNase A at -20°C.

Citations

Antonopoulos, R. K., Dadiotis, E., Ioannidis, K., Cheilari, A., Mitsis, V., Garcia-Campaña, A. M., … & Magiatis, P. (2025). Investigating the psychedelic hypothesis of kykeon, the sacred elixir of the Eleusinian Mysteries.
Boutsika, A., Deligiannidou, E., Moysiadis, T., Tourvas, N., Karnoutsos, P., Karagiovanidis, M., … & Ganopoulos, I. (2025). Molecular profiling and sex determination of Cannabis sativa germplasm collection: Exploring microsatellite markers and high-resolution melting (HRM) analysis. PeerJ, 13, e19770.
Cuenca-Medina, M., González-Mas, N., Martínez-Anguita, Ó., Sandoval-Lozano, A., & Quesada-Moraga, E. (2025). A new aphid IPM strategy based on the use of endophytic entomopathogenic ascomycetes that reduces treatment risks to the generalist predator Chrysoperla carnea (Stephens). Journal of Invertebrate Pathology, 108357.
Ordóñez, J., Pastrana, A. M., Borrero, C., Gómez, D., & Avilés, M. (2025). Preliminary findings on Clarireedia species associated with dollar spot in turfgrass in Spain. International Turfgrass Society Research Journal.
Christinaki, A. C., Myridakis, A. I., & Kouvelis, V. N. (2024). Genomic insights into the evolution and adaptation of secondary metabolite gene clusters in fungicolous species Cladobotryum mycophilum ATHUM6906. G3: Genes, Genomes, Genetics, 14(4), jkae006.
Alexandra M Kortsinoglou, Martyn J Wood, Antonis I Myridakis, Marios Andrikopoulos, Andreas Roussis, Dan Eastwood, Tariq Butt, Vassili N Kouvelis, (2024) Comparative genomics of Metarhizium brunneum strains V275 and ARSEF 4556: unraveling intraspecies diversity, G3 Genes|Genomes|Genetics,
García-Espinoza, F., García, M. J., Quesada-Moraga, E., & Yousef-Yousef, M. (2023). Entomopathogenic Fungus-Related Priming Defense Mechanisms in Cucurbits Impact Spodoptera littoralis (Boisduval) Fitness. Applied and Environmental Microbiology, e00940-23.
Fedoreyeva, L. I., Dilovarova, T. A., Vanyushin, B. F., Chaban, I. A., & Kononenko, N. V. (2022). Regulation of gene expression in Nicotiana tabacum seedlings by the MKASAA peptide through DNA methylation via the RdDM pathway. AIMS Biophysics, 9(2), 113-129.
Papaioannou, Charikleia, et al. “High Resolution Melting (HRM) Genotyping in the Genus Origanum: Molecular Identification and Discrimination for Authentication Purposes.”
Soffritti, G., Busconi, M., Sánchez, R. A., Thiercelin, J. M., Polissiou, M., Roldán, M., & Fernández, J. A. (2016). Genetic and Epigenetic Approaches for the Possible Detection of Adulteration and Auto-Adulteration in Saffron (Crocus sativus L.) Spice. Molecules, 21(3), 343.

Safety Statements

This product is developed, designed and sold exclusively for Research purposes and in vitro use only (RUO). The product was not tested for use in diagnostics or for drug development, nor is it suitable for administration to humans or animals. For more info, please check its Material Safety Data Sheet available in this website.