DNeasy Plant Pro Kits

For extraction of total cellular DNA from plant cells and tissues or fungi, or genomic DNA from plant cells, tissues and seeds

S_8770_DNeasyPlantPro
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DNeasy Plant Pro Kit (50)

Cat. No. / ID:  69204

Tissue Disruption Tubes, MB Spin Columns, Buffers, Collection Tubes (1.5 and 2 ml), for 50 preps
Preparations
50
250
DNeasy Plant Pro Kits are intended for molecular biology applications. These products are not intended for the diagnosis, prevention, or treatment of a disease.
Want to try this solution for the first time?
Get in touch with our team today and request a quote for your DNeasy Plant Pro Kit (50) trial kit.

Features

  • Superior PCR performance with patented Inhibitor Removal Technology (IRT)
  • Rapid extraction of ready-to-use DNA
  • No organic extraction, no ethanol precipitation
  • Highly efficient lysis and release of DNA from tough plant materials and associated plant pathogens

Product Details

The DNeasy Plant Pro Kit has several innovative features to overcome the challenges of DNA extraction from plant tissue and enable recovery of high-quality DNA from the toughest sample types, including strawberry leaf, grapevine leaf, pine needles and various seed types. Increased yields of plant DNA and plant pathogen DNA combined with superior removal of inhibitors ensure high-performance results in sensitive downstream applications.

Performance

The DNeasy Plant Pro Kit – the newest member of the trusted DNeasy Plant family – enables purification of significantly higher yields of DNA from the toughest sample types, including strawberry leaf, grapevine leaf, pine needles and various seed types (see table "Selection of plant species processed with DNeasy Kits" and see figure “ Significantly higher yields of pure DNA”). Patented Inhibitor Removal Technology (IRT) provides superior removal of inhibitors without using harsh chemicals, yielding pure DNA with less PCR inhibition (see figure “ Efficient removal of PCR inhibitors”).

When CT values of PCR reactions with plant DNA eluates containing possible inhibitors were compared to CT values of the PCR reaction with water added as control which does not inhibit amplification of the IC DNA, the eluate from the DNeasy Plant Pro Kit showed no inhibition.

With the DNeasy Plant Pro Kit, yields of DNA purified from strawberry leaf – a particularly tough plant sample – were significantly higher than those obtained using a kit from Supplier T and Supplier Z. Furthermore, the DNeasy Plant Pro Kit provided superior removal of inhibitors and the DNA eluate showed no inhibition (see figure “ Significantly higher yields and superior inhibitor removal”). The DNeasy Plant Pro Kit can also purify bacterial, fungal and viral DNA from plant and root samples.

The kit can be successfully combined into a workflow with proven products optimized for next-generation sequencing (NGS) (see figure “ Optimized NGS workflow”). Rapid and reliable identification of plant pathogens is crucial to avoid disease spread and facilitate effective disease management. Plant and pathogen DNA co-purified using the DNeasy Plant Pro Kit enables successful identification of a range of pathogens (see figure “ Successful identification of plant pathogens by NGS”)

Selection of plant species processed with DNeasy Kits
Abies alba (silver fir) Nicotiana tabacum (tobacco)
Aesculus hippocastanum (horse chestnut) Oryza sativa (rice)4
Arabidopsis thaliana (thale cress) Pelargonium sp. (geranium)4
Avena sp. (oat) Petunia sp.4
Brassica napus (oilseed rape) Pinus sylvestris (Scotch pine), P. brutia5
Brassica oleracea (kohlrabi) Populus tremula (aspen)
Chicorium endivia (chicory) Pseudotsuga menziesii (Douglas fir)
Citrullini lanatus (water melon) Quercus robur, Q. petrea (oak)6,7
Egeria sp. Rhododendron sp.2,4
Fagus sylvatica (beech)1 Rubus idaeus (raspberry)
Helianthus spp. (sunflower) Solanum tuberosum (potato)
Hordeum vulgare (barley)2 Sphagnum palustre (moss)
Humulus sp. (hops) Spinacia oleracea (spinach)
Hydrilla sp. Taxus baccata (yew)
Kalanchoe spp. Triticum aestivum (wheat)4
Lupinus sp. Ulmus glabra (elm)6
Lycopersicon esculentum (tomato)3 Vitis spp. (grape)6
Myriophyllum sp. Zea mays (maize)

 

See figures

Principle

The DNeasy Plant Pro Kit comprises a novel and proprietary method for fast and easy purification of total cellular DNA from plant cells, tissues and seeds. In addition, this kit can be used to purify bacterial, fungal and viral DNA from plant and root samples. The DNeasy Plant Pro Kit uses bead-beating technology, which replaces cumbersome DNA isolation procedures such as CTAB, phenol or chloroform extraction to recover high-quality DNA from the toughest sample types, including strawberry leaf, grapevine leaf, pine needles and various seed types. The DNeasy Plant Pro Kit uses the second generation of QIAGEN’s patented Inhibitor Removal Technology (IRT) to remove PCR inhibitors, including polysaccharides, polyphenolics and other secondary metabolites from plant extracts during the isolation process. Improved IRT, combined with efficient bead beating and lysis chemistry, results in high yields of inhibitor-free DNA that is ready for immediate use in downstream applications, including PCR, qPCR, and RAPD analysis, RFLP analysis, Southern blotting and next-generation sequencing.

 

Procedure

 

The DNeasy Plan Pro Kit uses bead-beating technology, whch replaces cumbersome DNA isolation procedures to recover high-quality DNA from the toughest sample types. Samples are added to the Tissue Disruption Tube which contains a specially shaped bead and a buffer for rapid homogenization (see figure " Rapid homogenization in Tissue Disruption Tubes"). Cell lysis and DNA release occur by mechanical and chemical methods. Released genomic DNA is cleared of PCR inhibitors using QIAGEN’s second-generation Inhibitor Removal Technology (IRT) and then captured on a silica membrane in a spin column format. DNA is then washed and eluted from the membrane and is ready for PCR, qPCR, NGS and other downstream applications.

An optional Phenolic Separation Solution step helps provide pure DNA even from samples with high polyphenolic compounds, such as pine or grape leaves by breaking the bonds between DNA and phenolics. This step prevents DNA loss that would otherwise occur in these samples.


The DNeasy Plant Pro Kit is used with a vortexer or high-velocity bead beating, based on sample needs. Vortex methods work with soft leaf tissue. High-velocity bead beaters, like the PowerLyzer 24 Homogenizer or the TissueLyser II, break down tougher plant material such as roots, seeds, stems or challenging leaf tissues. Furthermore, purification of DNA using the DNeasy Plant Pro Kit can be fully automated on the QIAcube Connect.

 

See figures

Applications

DNeasy Plant Kits provide purification of ready-to-use DNA from plant samples, including plant cells, plant tissues and fungi.
The DNeasy Plant Pro Kit is designed for:

  • DNA extraction from plants and plant-associated microorganisms
  • PCR and NGS analysis
  • Marker-assisted breeding
  • Plant pathogen research
  • Studies on genetically modified plants
  • Detection of resistance traits

 

Comparison of DNeasy Plant Pro and Plant Kits
Features DNeasy Plant Mini Kit DNeasy Plant Maxi Kit DNAeasy 96 Plant Kit DNeasy Plant Pro Kit
Applications PCR, qPCR, blotting, next-generation sequencing PCR, qPCR, blotting, next-generation sequencing PCR, qPCR, blotting, next-generation sequencing PCR, qPCR, blotting, next-generation sequencing
Elution volume 50–200 µl 500 µl – 2 ml 100–200 µl 50–100 µl
Format Spin column Spin column 96-well plate Spin column
Main sample type Plant samples Plant samples Plant samples Plant samples and seeds
Bead size N.A. N.A. N.A. 5/32” (3.9 mm) ballcone
Binding capacity Up to 50 µg Up to 500 µg Up to 50 µg (per well) Up to 50 µg
Processing Manual Manual Manual Bead beating
Purification of total RNA, miRNA, poly A+ mRNA, DNA or protein DNA DNA DNA DNA
Sample amount Up to 100 mg Up to 1 g Up to 50 mg Up to 100 mg
Technology Silica technology Silica technology Silica technology Silica technology
Throughput Varies Varies 96 or 192 samples Varies
Time per run or per prep <1 hour <2 hours <2 hours (192 samples) 45 minutes (24 samples)
Typical yield (from 50 mg starting material) Up to 30 µg Up to 260 µg Up to 15 µg Up to 30 µg

N.A. = Not applicable

Supporting data and figures

Resources

Safety Data Sheets (1)
Certificates of Analysis (1)

Publications

Identification of a gene in the process of being lost from the genus Agrostis.
Li HM; Rotter D; Bonos SA; Meyer WA; Belanger FC;
Plant Physiol; 2005; 138 (4):2386-95 2005 Jul 1 PMID:15995002
Power and limitations of the chloroplast trnL (UAA) intron for plant DNA barcoding.
Taberlet P; Coissac E; Pompanon F; Gielly L; Miquel C; Valentini A; Vermat T; Corthier G; Brochmann C; Willerslev E;
Nucleic Acids Res; 2006; 35 (3):e14 2006 Dec 14 PMID:17169982
Defective RNA processing enhances RNA silencing and influences flowering of Arabidopsis.
Herr AJ; Molnàr A; Jones A; Baulcombe DC;
Proc Natl Acad Sci U S A; 2006; 103 (41):14994-5001 2006 Sep 28 PMID:17008405
Genetic diversity in three groups of barley germplasm assessed by simple sequence repeats.
Matus IA; Hayes PM;
Genome; 2002; 45 (6):1095-106 2002 Dec PMID:12502254
Transposition-based plant transformation.
Yan H; Rommens CM;
Plant Physiol; 2006; 143 (2):570-8 2006 Dec 1 PMID:17142486