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
US$165.00
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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
  • Process up to 384 samples on the QIAsprint Connect with zero manual intervention after the run starts
  • 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 Ct 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 ΔCt 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).

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 and Guides (2)

Catalyze confidence in every reaction

Overview of the QIAsprint Connect system
Kit Handbooks (3)
Highly pure, nuclease-free water for use in all molecular biology applications
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 buffer should be used to dilute cDNA made using the miScript Reverse Transcription Kit?

cDNA generated with the miScript Reverse Transcription Kit can be diluted either with Nuclease-Free Water or TE buffer.

 

 

FAQ-1601
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
I get low DNA yield. What can I do?
Ensure that the starting material is completely disrupted and homogenized.  Some plant tissues may require more or less bead beating than recommended. Requirements can vary substantially between species and between different portions of the plant. Therefore, individual sample types should be assessed to determine optimal conditions.
FAQ-4230
I get low DNA yield. What can I do?
Increase the volume of Buffer RLT used for lysis to up to 500–600 μL, but process only the recommended 300 μL of lysate for DNA purification. Polyphenolic compounds may be copurified with some plant materials, and these compounds can inhibit downstream reactions. Polyphenols can be removed by adding 33 mg/mL insoluble polyvinyl polypyrrolidone (PVP) to Buffer RLT before use. PVP forms hydrogen-bonded complexes with polyphenolic compounds, which are then separated from the DNA during the lysate centrifugation step. Prepare a small aliquot of Buffer RLT containing 33 mg/mL PVP and thoroughly vortex the modified lysis buffer before use.
FAQ-4231
My plant lysate becomes very viscous after disruption. What can I do?
Reduce the input amount, ensure efficient but not excessive mechanical disruption, or increase the lysis buffer volume as suggested. Avoid overgrinding, especially for fresh or soft tissues.
FAQ-4232
I am targeting the plant-associated bacteria. Is there a difference in the lysis options?
The optimal lysis method depends on the plant tissue and the target. Mechanical disruption is effective for most plant tissues but may shear high‑molecular‑weight DNA. When targeting plant‑associated bacteria, the use of small‑sized beads or PowerBead tubes or plates is recommended. In these cases, increasing the lysis buffer volume can further improve bacterial lysis and DNA recovery.
FAQ-4233
How much plant tissue can I use?
The optimal input amount depends on the sample type. Although DNA can be extracted from up to 100 mg of material, it is generally recommended not to exceed 50 mg of fresh plant tissue. For many ground seeds or beans, 30 mg of material is sufficient and provides optimal performance.
FAQ-4234
I see beads in my elution plate. Is this a problem, and what can I do?
Beads can be a result of high input amounts. If possible, reduce the amount of sample. To proceed with the eluate, place the samples onto a magnet rack and remove cleared supernatant.
FAQ-4235
Why is my eluate discolored, and why are my 260/230 ratios lower than expected after DNA isolation from plant tissue?
Some plant tissues, particularly those rich in secondary metabolites, pigments, or polysaccharides, may cause discoloration and reduced 260/230 ratios. Reducing the input amount or adding Buffer ATL, as described in the protocol,  might help in reducing the interfering contaminant in the eluate. 
FAQ-4236
Which PrepSet should I chose for my samples DNA/RNA Plant PrepSet or PowerExtract IRT PrepSet?
Choosing the PrepSet depends on the plant material and the intended downstream application. The DNA/RNA Plant PrepSet is suitable for DNA extraction from a wide range of plant tissues, including many inhibitor‑rich samples. However, for some challenging plant materials, DNA quality may be reduced. The PowerExtract IRT PrepSet is more efficient for plants rich in inhibitors (e.g., polyphenols or polysaccharides) and provides improved DNA quality and robustness for sensitive downstream.
FAQ-4237
I got green-, red-, or yellow-colored eluates. What should I do?
Chlorophyll or carotenoids can be removed efficiently by adding one additional wash step using Buffer AW2 or 100% ethanol in future preparations. Alternatively, reducing the amount of starting material to the recommended amount. Slight color in the eluate does not necessarily interfere with downstream applications. You can also add Buffer ATL, reduce Buffer RLT volume to 300 µL, and supplement with 100 µL Buffer ATL. Optionally, add 1 µL Reagent DX  to minimize foaming. Disrupt and homogenize the plant material then centrifuge the lysate as describe.
FAQ-4238
How many buccal swab samples can be processed with the QIAsprint DNA Tissue/Cells PrepSet?
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 is sufficient for processing 200 buccal swab samples, and the supplied volume of Proteinase K is sufficient for processing 300 buccal swab samples.
FAQ-4251