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QIAsprint modular system: Automated plant DNA and RNA isolation

Automates high-throughput plant DNA/RNA isolation. Process up to 384 samples for consistent, downstream application-ready nucleic acids

S_1084_5_GEN_V2

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QIAsprint DNA/RNA Plant PrepSet (384)

Cat no. / ID.   580669

Buffer RLT for 384 DNA/RNA preparations from plant samples
¥25,000
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Kit
PrepSet
Essential Kit
Add on
QIAsprint Consumables
Type
Plant Tissue
Inhibitor-rich
QIAsprint DNA/RNA Plant PrepSet (384) is intended for molecular biology applications. This product is not intended for the diagnosis, prevention, or treatment of a disease.
The QIAsprint modular system: Automated plant DNA and RNA isolation is intended for molecular biology applications. This product is not intended for the diagnosis, prevention, or treatment of a disease.

✓ 24/7 automatic processing of online orders

✓ Knowledgeable and professional Product & Technical Support

✓ Fast and reliable (re)-ordering

Features

  • Purify genomic DNA and RNA from up to 50 mg of diverse plant tissues
  • Combine application specific PrepSets with Essential Kits for flexible modular protocols
  • Remove secondary metabolites and PCR inhibitors using specialized IRT technology
  • Simplify logistics with modular components that ship and store at ambient temperature

Product Details

The QIAsprint modular system for DNA/RNA extraction from plants is designed for high-throughput nucleic acid isolation using magnetic bead purification. The modular system enables fully automated processing on the QIAsprint Connect instrument without manual intervention after run start, including an optional fully automated onboard lysis step.

The kit consists of dedicated modules that can be combined or exchanged depending on sample type and workflow requirements.

For genomic DNA isolation from plant cells and tissues, we recommend the following modules:

QIAsprint DNA/RNA Plant PrepSet (384): Designed for efficient pretreatment and lysis of plant samples.

QIAsprint Essential Kit A (384): Provides the beads and wash buffers required for DNA/RNA purification, ensuring high yield, reproducibility and recovery of high-quality nucleic acids.

For inhibitor-rich plant samples, the QIAsprint PowerExtract IRT PrepSet can be combined with Essential Kit A (384) to reduce co-purified inhibitors (see  QIAsprint DNA Plant workflow). 

All modules are optimized for fully automated processing of up to 384 samples on the QIAsprint Connect, enabling minimal hands-on time and reproducible performance.

Performance

The QIAsprint DNA/RNA Plant workflow application delivers high DNA yield across various plant tissues, including leaves and seeds (see  DNA yield from various plant tissues).

In qPCR analysis targeting the chloroplastic rbcL gene, DNA extracted with QIAsprint DNA/RNA Plant PrepSet showed comparable or lower Cq values than the MagMAX Plant DNA Isolation Kit (Thermo Fisher Scientific) (see  qPCR comparison of QIAsprint DNA/RNA Plant PrepSet and MagMAX Plant DNA Isolation Kit). For inhibitor-rich samples, the QIAsprint PowerExtract IRT PrepSet showed no detectable PCR inhibition based on ΔCq analysis, including challenging materials such as faba beans, whereas inhibition was observed with the comparator kit (see  PCR inhibition assessment between QIAsprint PowerExtract IRT PrepSet and MagMAX Plant DNA Isolation Kit).

Principle

The QIAsprint modular system for DNA/RNA extraction from plants enables automated high-throughput purification of total DNA, including genomic, chloroplast and mitochondrial DNA and RNA from plant material such as leaves and seeds. Magnetic particle technology enables purification of high-quality nucleic acids free of proteins, nucleases and other contaminants. The purified nucleic acids are ready for use in sensitive downstream applications such as amplification and other enzymatic reactions. For purification of DNA from inhibitor-rich plants or plant-associated bacteria and fungi, the QIAsprint PowerExtract IRT PrepSet is available for use.

If the workflow needs to be adapted for other sample types or input materials, the flexibility of the QIAsprint modular kit allows the combination of the QIAsprint Plant DNA/RNA PrepSet with other compatible Essential Kits.

In addition, most buffers and reagents used within the workflow are available as standalone components, enabling further customization for specialized applications (see QIAsprint sets and consumables finder).

See QIAsprint Connect Protocol Guide for support on finding or customizing according to your application’s needs.

Procedure

Fresh, frozen or lyophilized plant material, up to 50 mg per sample, is mechanically homogenized (e.g., TissueLyser III). The homogenate is resuspended in lysis buffer, mixed and clarified by brief centrifugation.

For inhibitor-rich samples, an optional Inhibitor Removal Technology (IRT) buffer step can be included after lysis to reduce co-purified inhibitory substances.

Cleared lysates are transferred to the QIAsprint Prep Plate Insert (32) (cat. no. 582226). Wash and elution plates are prepared according to the protocol and loaded onto the QIAsprint Connect. The system then performs fully automated magnetic bead-based binding, washing, drying and elution. Purified DNA is eluted in water or low-salt buffer and is ready for downstream applications such as PCR and other enzymatic reactions.

Applications

DNA purified with the QIAsprint Plant DNA workflow is highly suitable for RT-PCR, digital PCR (dPCR) or next-generation sequencing (NGS) as well as long-read sequencing application (depending on disruption and lysis method).

Supporting data and figures

Specifications

FeaturesSpecifications
ApplicationsRT-PCR, dPCR, NGS, long-read sequencing
Elution volumeVariable, depending on protocol 50 µL and 100 µL recommended
Main sample typeVarious samples from plant
ProcessingAutomated  on QIAsprint
AnalyteGenomic DNA
Sample amountUp to 50 mg is recommended but up to 100 mg is possible based on the input material
TechnologyMagnetic-particle technology

Sets & Consumables

QIAsprint Sets
Add ons
Consumables & Accessories

Resources

Brochures & Guides (3)
QIAsprint Connect Protocol Guide
LITERATURE (17.7KB)
Support on finding or customizing protocols according to your application's needs.
Overview of the QIAsprint Connect system

Catalyze confidence in every reaction

Kit Handbooks & Protocols (5)
Highly pure, nuclease-free water for use in all molecular biology applications
Scientific documents (1)
Evaluate automated DNA isolation from inhibitor-rich stool samples using QIAsprint Connect for high-throughput microbiome and molecular analysis.
Safety Data Sheets (1)
Download Safety Data Sheets for QIAGEN product components.
Certificates of Analysis (1)
Operating software (1)
Note: Unzip the folder prior to protocol installation on the QIAsprint Connect.
User Manuals (1)
QIAsprint Connect User Manual
PDF (14.7MB)
Download

FAQ

How do I safely inactivate biohazardous flow-through material?

Always dispose of potentially biohazardous solutions according to your institution’s waste-disposal guidelines. Although the lysis and binding buffers in QIAamp, DNeasy, and RNeasy kits contain chaotropic agents that can inactivate some biohazardous material, local regulations dictate the proper way to dispose of biohazards. DO NOT add bleach or acidic solutions directly to the sample-preparation waste. Guanidine hydrochloride in the sample-preparation waste can form highly reactive compounds when combined with bleach.
Please access our Material Safety Data Sheets (MSDS) online for detailed information on the reagents for each respective kit.

FAQ-12
What is the pH value of QIAGEN's Nuclease-Free Water?

At 22°C, Nuclease-Free Water has a pH value of between 5.0 and 6.5. It is not possible to determine the pH of highly pure water exactly. Therefore, many publications/industry standards do not provide a pH specification for highly pure water. Highly pure water does not contain enough ions or impurities for an exact pH determination. In general, values between pH 5 and 8 are obtained.

FAQ-1290
Is your Nuclease-Free Water fluorescence-free?

Yes, QIAGEN's Nuclease-Free Water is distilled water that is completely free of substances that may fluoresce.

 

FAQ-1291
What quality level does your Nuclease-Free Water have?

Nuclease-Free Water has been prepared without the use of chemicals such as DEPC (diethylpyrocarbonate) using an in-house method. The high quality of the water is assured by testing for DNase, RNase, and microbial contamination during the production process.

FAQ-1292
What is the composition of Buffer RLT?

The exact composition of Buffer RLT is confidential. This buffer is a proprietary component of RNeasy Kits. Buffer RLT contains a high concentration of guanidine isothiocycanate, which supports the binding of RNA to the silica membrane. Buffer RLT can be purchased separately (cat. no. 79216)

Note: note that ß-mercaptoethanol should be added to Buffer RLT before use to effectively inactivate RNAses in the lysate (10 µl ß-Mercaptoethanol per 1 ml Buffer RLT).

FAQ-2793
3314-What is the concentration of RNase A sold separately?

RNase A (17500 U), catalog number 19101, is 100mg/ml. 

RNase A Solution (650 µl), catalog number 158922, and RNase A Solution (5 ml), catalog number 158924, are both 4mg/ml.

FAQ-3314
Can I use other plastics than the QIAsprint Connect plastics on the instrument?
No, this is not possible. The QIAsprint Connect plastics are designed to fit into the frames that are transported on the workdeck by the gripper in a stable way. Other plastics would not fit in there. 
FAQ-4201
What sample type can be processed using the QIAsprint PowerExtract IRT PrepSet?
The QIAsprint PowerExtract IRT PrepSet can be combined with Essential Kit C for processing fresh and frozen stool samples and wastewater. When paired with Essential Kit A, it is suitable for inhibitor-rich plant materials such as seeds and beans.
FAQ-4210
Which sample amounts can be processed with the QIAsprint PowerExtract IRT PrepSet + Essential Kit C?
Use 1–100 mg stool material. It is recommended to start with 50 mg. An easy way to transfer stool material without weighing is to use a 10 µL or 1 µL inoculating loop.
FAQ-4211
What are the elution volume and the elution buffer?
The elution buffer is RNase-free water, and elution volume is 100 µL.
FAQ-4212
Which sample disruption options are available for stool samples?
Disruption in 2 mL PowerBead Pro tubes can be used to achieve optimal RNA and DNA quality and purity when following the recommended protocol with phenol–chloroform–isoamyl alcohol (PCIA). For the high-throughput approach, PowerBead Pro Plates can be used with an adapted protocol, as PCIA is incompatible with the sealing foil on the plate. In the modified protocol, PCIA is added only after sample disruption and is important for the extraction of high-quality RNA. If only DNA is to be extracted, PCIA can be omitted, although this may result in slightly lower yields and reduced inhibitor removal, depending on the stool sample. A new high-throughput disruption format (CMTR-based) will be developed post-launch.
FAQ-4213
Do I need additional equipment to work with the QIAsprint PowerExtract IRT PrepSet?
For sample disruption, a vortex adapter for the Vortex-Genie 2 is required when using PowerBead Pro tubes, or a TissueLyser III when working with PowerBead Pro Plates. For centrifugation, a benchtop centrifuge that accommodates either 2 mL tubes or 96-well plates is required.
FAQ-4214
Are there any critical steps in the protocol?
Avoid transferring any of the pellet after centrifugation. Perform the disruption step as described in the protocol, as deviations may affect yield and diversity.
FAQ-4215
Are there possible stopping points in the protocol?
Yes, the supernatant from disruption and centrifugation can be stored for 2 hours at room temperature and overnight at 2– 8°C. For longer storage, the supernatant should be stored at −20°C (storage beyond 4 weeks has not been tested).
FAQ-4216
I see precipitates in Solution CD2. What should I do?
Solution CD2 should be stored at 2–8°C upon arrival. If stored at room temperature for extended periods, precipitates may form. This reaction is irreversible. Do not use the solution and replace it with a new bottle (cat.no. 47016-2).
FAQ-4217
How many buccal swab samples can be processed with the QIAmini DNA Tissue/Cells Kit?
Due to the higher volume of Buffer ATL and Proteinase K required for processing buccal swabs, additional components may need to be purchased. The supplied volume of Buffer ATL will be sufficient for processing 30 buccal swab samples.
FAQ-4250