用于从植物细胞和组织或真菌中提取总细胞 DNA，或从植物细胞、组织和种子中提取基因组 DNA

Features

具有专利的抑制剂去除技术 (IRT) 的卓越 PCR 性能
快速提取即用型DNA
无有机萃取，无乙醇沉淀
从坚韧的植物材料和相关植物病原体中高效裂解和释放 DNA

Product Details

DNeasy Plant Pro Kit 具有多项创新功能，可克服从植物组织中提取 DNA 的挑战，并能够从最棘手的样品类型
（包括草莓叶、葡萄叶、松针和各种种子类型）中回收高质量的 DNA。植物 DNA 和植物病原体 DNA 产量的增加
以及抑制剂的卓越去除确保了敏感下游应用中的高性能结果。
DNeasy Plant Kits 以离心柱形式从植物样品中快速简便地分离出基于二氧化硅的 DNA。典型产量为 3–260 μg
高质量 DNA，具体取决于所用样品（例如小麦、玉米、拟南芥、番茄、烟草）和 DNeasy 硅胶膜的结合能力。
DNeasy Plant Kits 还以方便的 96 孔板形式提供基于二氧化硅的 DNA 纯化，典型产量为 1–15 µg DNA，具体
取决于植物物种。 QIAcube Connect 也可自动从植物组织中分离 DNA。

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 . Patented Inhibitor Removal Technology (IRT) provides superior
removal of inhibitors without using harsh chemicals, yielding pure DNA with less PCR inhibition.

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 . 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) . 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”).

DNeasy Plant Kits allow rapid and efficient isolation of high-quality DNA from a wide variety of plant species and tissue types, including the most demanding sources
 (see table "Selection of plant species processed with DNeasy Kits"). Samples may be fresh, frozen or dried. The optimized DNeasy Plant procedure incorporates the QIAshredder
 spin column, a unique filtration and homogenization column that efficiently removes cell debris and improves sample handling following lysis.

The typical yield is 3–260 µg, with a sample size of up to 1 g wet weight, and an elution volume of 50 µl to 2 ml. DNA yields vary between different species and tissues
 depending on genome size, ploidy, cell number and tissue sample age.

The DNeasy Plant procedure yields pure nucleic acid, free of polysaccharides and other secondary metabolites often copurified using conventional methods. Such impurities
can interfere with spectrophotometric readings and inhibit enzymatic reactions. Absorbance scans of DNeasy purified DNA show a symmetrical peak at 260 nm (see figures "
 DNA purity from oak leaves and pine needles"), confirming that the DNA is free of impurities, including enzyme inhibitors. DNeasy purified DNA is sized up to 40 kb (see
 figure "Pure DNA (20–25 kb) for restriction analysis"). Purified DNA can be used in a wide range of applications (see figures "PCR analysis" and "RAPD analysis").

High-quality DNA can be isolated from 96 or 192 samples of plant leaf tissue in less than 2 hours. The simple 96-well procedure provides highly reproducible yields of total
cellular DNA (see figure "Uniformity of DNA yields from 96 wheat samples"). The typical yield is 1–15 µg per 50 mg plant leaf tissue, with an elution volume of 100–200
 µl. DNA yields vary between species depending on genome size, ploidy, cell number and tissue sample age.

Procedure

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.

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.

Samples are first mechanically disrupted and then chemically lysed (see flowchart "DNeasy Plant and DNeasy 96 Plant procedures"). RNA is removed by RNase digestion during
 lysis. Cell debris, precipitated proteins and polysaccharides are removed and the sample is homogenized by centrifugation through a QIAshredder spin column. Buffering
 conditions are adjusted and the lysate is loaded onto a DNeasy Plant spin column or 96-well plate. During a brief spin, DNA selectively binds to the silica membrane while
contaminants pass through. The remaining contaminants and enzyme inhibitors are removed in one or two efficient wash steps. Pure DNA is then eluted in water or low-salt
 buffer, ready for use.

Purification of DNA using the DNeasy Plant Mini Kit can be automated on the QIAcube Connect.

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