QIAsprint modular system: Automated DNA extraction from tissue and cells

For automated purification of genomic DNA from tissues and cells on the QIAsprint Connect instrument

S_1084_5_GEN_V2

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QIAsprint DNA Tissue/Cells PrepSet (384)

Cat no. / ID.   587449

Buffer ATL, Buffer VXL, Buffer ACB, Proteinase K, and Reagent DX for 384 DNA preparations from tissue or cell samples
Kit
PrepSet
Essential Kit
Add on
QIAsprint Consumables
QIAsprint modular system: Automated DNA extraction from tissue and cells are intended for molecular biology applications. These products are 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

  • Extract high-yield DNA from tissue or cells, ensuring high-quality DNA recovery
  • Customize gDNA extraction protocols for specific applications using modular kit components
  • Eliminate manual intervention with fully automated processing on the QIAsprint Connect
  • Remove dry ice requirements with ambient temperature shipping

Product Details

The QIAsprint workflow for genomic DNA isolation from tissue and cells is a modular magnetic-bead-based system for high-throughput DNA purification using the QIAsprint Connect system. The workflow combines modular workflow design with magnetic-bead technology, enabling fully automated processing without manual interaction.

The workflow consists of dedicated modules that can be flexibly combined or exchanged depending on sample type and workflow requirements. For genomic DNA isolation from tissue and cells, we recommend the following modules:

QIAsprint DNA Tissue/Cells PrepSet (384): Designed for efficient pretreatment of tissue and cell samples. This module provides Buffer ATL for cell lysis and Proteinase K for protein digestion prior to automated purification.

QIAsprint Essential Kit C (384): Supplies the magnetic beads and wash buffer required for DNA purification. Magnetic-bead technology enables efficient binding, washing and elution to obtain high-quality genomic DNA.

All modules are optimized for automated processing of up to 384 samples on the QIAsprint Connect, enabling scalable high-throughput DNA purification with no manual intervention during run.

Performance

The QIAsprint DNA Tissue/Cells workflow delivers DNA yields comparable to or higher than those obtained with other leading magnetic-bead-based purification systems. This performance is consistent even with challenging sample types as fibrous tissues or fatty (see Comparative analyses of DNA yield from tissue and cells).

The QIAsprint DNA Tissue/Cells workflow enables efficient purification of genomic DNA from various biological materials compared to leading magnetic-bead-based purification systems. The purified DNA provides reliable quality suitable for downstream analyses such as qPCR and dPCR (see Comparative analyses of qPCR amplification for DNA extracted from tissue and dPCR amplification of DNA extracted from tissue samples).


 

Principle

The QIAsprint DNA Tissue/Cells workflow uses a modular approach to enable efficient and flexible DNA purification on the QIAsprint Connect. Sample pretreatment is performed using the QIAsprint DNA Tissue/Cells PrepSet (384), in which Buffer ATL and Proteinase K digestion enable complete lysis, even of tough tissue types. The QIAsprint Essential Kit C (384) then provides the magnetic beads and buffers required for the automated bind, wash and elute steps on the instrument. During processing, DNA binds to the magnetic beads, contaminants are efficiently washed away, and high-quality DNA is eluted for downstream analysis.

For other samples types or input material, the flexibility of the QIAsprint modular workflow allows users to combine the QIAsprint DNA Tissue/Cells PrepSet with other compatible Essential Kits. In addition to combining different modules, nearly all buffers and reagents used within the system are available as standalone items, providing additional customization options for specialized workflows (see QIAsprint sets and consumables finder).

Procedure

In the QIAsprint DNA Tissue/Cells workflow, samples undergo straightforward pretreatment and an automated purification process. Cell pellets are first homogenized, while tissue samples are disrupted and homogenized in Buffer ATL. Proteinase K is then added, and samples are incubated to achieve complete enzymatic digestion and efficient lysis (see  QIAsprint DNA tissue/cells workflow).

Following incubation, the lysates are transferred to the prep plate and combined with MagG Bead Suspension in a binding master mix to enable efficient DNA binding. Wash plates and the elution plate are prepared according to the protocol and placed into the plate hotels. All plates and hotels are then loaded onto the QIAsprint Connect, and the appropriate protocol is selected. The instrument performs fully automated magnetic-bead-based bind, wash and elute steps. 

Applications

DNA purified with the QIAsprint DNA Tissue/Cells workflow is highly suitable for RT-PCR, digital PCR (dPCR) or next-generation sequencing (NGS) as well as long-read sequencing applications (depending on the 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 200 µL recommended
Main sample typeCells, tissue
ProcessingAutomated on QIAsprint Connect
AnalyteGenomic DNA
Sample amountUp to 50 mg (fresh) or 25 mg (stabilized) tissue or up to 5 x 106 cells
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 (2)
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

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
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
When resuspending my cell pellet, the sample gets very viscous. What can I do?
For high cell numbers and/or certain cell lines, this may happen for >1 × 106 cells. Using homogenization methods like the TissueLyser III, TissueRuptor II, vortex with respective adaptor, or passing the sample through a needle will help.
FAQ-4244
Is there a difference in the lysis options mentioned for tissue samples?
The most efficient lysis option depends on the tissue type. For many tissues, mechanical disruption may be the most efficient solution, and DNA will be suitable for downstream assays. However, this may lead do shearing of very long DNA fragments.
FAQ-4245
How much tissue can I use?
Up to 50 mg of fresh-frozen tissue and up to 25 mg of stabilized tissue can be used. For DNA-rich tissues like spleen, starting amounts should not exceed 10 and 5 mg, respectively. 
FAQ-4246
I see some beads in my elution plate. Is this a problem, and what can I do?
Residual beads can result from high input amounts; if possible, reduce the amount of sample. Ensure that Proteinase K has been used for optimized lysis. To continue with the eluate, place the samples on a magnetic rack and remove the cleared supernatant.
FAQ-4247
Why is my eluate discolored after DNA isolation from tissue?
For some tissues, especially those rich in blood, discoloration may occur. Using Buffer RDW in the second wash step instead of 80% ethanol may resolve the issue.
FAQ-4248
Which protocol should I chose?
For tissue and cell samples, two protocol options are recommended, with a 200 µL elution to recover DNA efficiently. The extended air-dry option may be beneficial when high volumes of undiluted eluate will be used in downstream assays known to be sensitive to alcohol carry over. For low-biomass samples such as buccal swabs, a protocol with a lower elution volume is recommended.
FAQ-4249
I would like to process more than 200 µL lysate?
Processing higher sample volumes can be achieved by adjusting the protocol by adding a second (or more) lysate plate. In this plate, lysate and binding master mix without MagG Bead Suspension are added. During the extraction, the magnetic particles are transferred from the first lysate plate into the next, allowing for use of twice as much. 
FAQ-4250
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