QIAsprint modular system: Automated pathogen DNA and RNA extraction

For automated purification of pathogen DNA and RNA from plasma, serum and cell-free body fluids

S_1084_5_GEN_V2

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QIAsprint Pathogen PrepSet (384)

Cat no. / ID.   585799

Buffer ACL, Proteinase K, and Carrier RNA for 384 preparations of viral DNA,RNA and bacterial DNA extraction
€605.00
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Kit
PrepSet
Essential Kit
Add on
QIAsprint prep sets, Essential Kits and Add Ons  are intended for molecular biology applications. These products are not intended for the diagnosis, prevention, or treatment of a disease.
The QIAsprint Pathogen 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 pathogen DNA and RNA extraction 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

  • Recover low-abundance pathogen DNA and RNA with high reliability using magnetic-bead technology
  • Combine QIAsprint Pathogen PrepSet with Essential Kit A to optimize lysis, binding, washing and elution
  • Deliver purified nucleic acids ready for PCR, RT-PCR, qPCR and sequencing
  • Choose between onboard lysis for true walk-away automation or offboard lysis for added flexibility

Product Details

The QIAsprint workflow for pathogen nucleic acid isolation from body fluids is a modular, magnetic-bead–based solution for automated purification of pathogen DNA and RNA. The worfklow enables streamlined processing on the QIAsprint Connect, supporting both onboard and offboard lysis. Dedicated modules can be combined as needed to accommodate different sample types and workflow preferences.

For pathogen DNA and RNA isolation from body fluids, swabs or transport media, we recommend the following modules:

QIAsprint Pathogen PrepSet (384): Designed for efficient lysis of pathogens in complex, inhibitor-rich sample materials. The PrepSet enables the addition of Proteinase K, sample and lysis/binding chemistry either directly into the sample plate for onboard lysis or as a pre-incubation step for offboard lysis.

QIAsprint Essential Kit A (384): Provides the magnetic beads and optimized wash chemistry required for the efficient removal of inhibitors commonly present in pathogen samples. The bead-based technology ensures reliable recovery of low-abundance pathogen DNA and RNA.

All modules are optimized for the fully automated processing of up to 384 samples on the QIAsprint Connect. Depending on the selected workflow, lysis can be performed onboard the instrument for true walk-away automation or offboard to increase flexibility.

Performance

The QIAsprint Pathogen PrepSet in combination with QIAsprint Essential Kit A delivers robust, fully automated purification of pathogen DNA and RNA from complex body fluid and swab samples.

Two validated workflow options provide flexibility depending on laboratory priorities: the onboard lysis workflow enables automation, with all steps performed on the QIAsprint Connect without user interaction, whereas the offboard lysis workflow enables flexible workflow adaptation and competitive processing times (see  QIAsprint pathogen workflow).

For pretreatment of difficult-to-lyse bacteria, mechanical and chemical lysis using bead beating efficiently helps release bacterial nucleic acids. For this type of lysis, Pathogen Lysis Tubes S (cat. no. 19091, including Reagent DX) or Pathogen Lysis Tubes L (cat. no. 19092, including Reagent DX) can be used. Alternatively, the PowerBead Pro Tube (cat. no. 19301) or the PowerBead Pro Plate (cat. no. 19311) are recommended. The choice of Pathogen Lysis Tube variant, PowerBead Pro Tube or Plate depends on the pathogen target.

Performance data generated in QIAGEN internal studies comparing the QIAsprint workflow with commonly alternative pathogen nucleic acid extraction kits demonstrate reliable nucleic acid recovery across diverse pathogen types and challenging sample matrices. Consistent linear RT-qPCR performance is observed for viral RNA and DNA across various sample types, confirming effective inhibitor removal (see  RT-qPCR performance from different starting materials). Digital PCR comparison with a platform from a different supplier demonstrates equivalent or improved recovery performance across viral titers (see  Competitor comparison by dPCR).

Principle

The QIAsprint Pathogen PrepSet combines the speed and efficiency of silica-based nucleic acid purification with the convenient handling of magnetic particles. The purification procedure is designed to ensure safe and reproducible handling of potentially infectious samples. The purification procedure comprises four steps: lyse, bind, wash and elute. Proteolysis of viruses and bacteria in the samples is performed under highly denaturing conditions at elevated temperatures. Lysis is performed in the presence of Proteinase K and lysis buffer, which ensures digestion of viral coat proteins, bacterial membrane proteins and inactivation of RNases.

In addition to combining different modules, nearly all buffers and reagents used within the system are available as standalone items, offering additional customization options for specialized workflows (see QIAsprint sets and consumables finder).

Procedure

The QIAsprint pathogen workflow uses a modular magnetic-bead-based approach for the automated purification of pathogen nucleic acids from cell-free body fluids.

The procedure combines the QIAsprint Pathogen PrepSet for optimized pathogen lysis with QIAsprint Essential Kit A, which provides magnetic beads and wash chemistry to remove inhibitors commonly present in body fluids or transport media.

Depending on workflow preference, lysis can be performed:

  • Onboard the instrument by adding Proteinase K, sample and lysis/binding mix directly into the sample plate
  • Offboard by incubating the sample with lysis reagents prior to loading onto the instrument

In both cases, nucleic acids bound to magnetic beads are automatically transferred through multiple wash steps and are finally eluted as highly pure DNA and RNA suitable for sensitive downstream detection (see  QIAsprint pathogen workflow).

Applications

Pathogen DNA and RNA purified with the QIAsprint pathogen workflow are ideally suited for sensitive downstream detection methods such as RT-PCR, qPCR, digital PCR (dPCR) and next-generation sequencing (NGS).

Supporting data and figures

Specifications

FeaturesSpecifications
ApplicationsRT-PCR, qPCR, dPCR, NGS
Elution volumeVariable, depending on sample 50 µL and 100 µL recommended
Main sample typeSerum, plasma, blood, body fluids, swabs, transport media
ProcessingAutomated on QIAsprint
AnalytePathogen DNA and RNA
Sample amount200 µL
TechnologyMagnetic-particle technology

Sets & Consumables

QIAsprint Sets
Add ons
Consumables & Accessories

Resources

Brochures and Guides (2)
Overview of the QIAsprint Connect system
Kit Handbooks (1)
Highly pure, nuclease-free water for use in all molecular biology applications
Protocols (1)
Safety Data Sheets (1)
Download Safety Data Sheets for QIAGEN product components.
Certificates of Analysis (1)

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
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
I get low nucleic acid yield. What can I do?
Ensure thorough lysis. Proper mixing of the lysis/binding mix of Buffer ACL, isopropanol, carrier RNA, and MagG Bead Suspension is critical. Check sample pretreatment: some matrices (e.g., viscous) may require pretreatment as described in the handbook.
FAQ-4218
What sample volume can I process?​
Standard input is 200 µL sample per well. If you need to process larger volumes, you can modify the protocol by introducing a second (or additional) lysate plate. In this approach, the lysis/binding  mix — without MagG Bead Suspension — is added to the additional plate(s). During extraction, the magnetic particles are transferred from the first lysate plate into the subsequent plate(s), allowing you to process double the sample volume or more. 
FAQ-4219
Can I skip Proteinase K?​
It is not recommended to skip the Proteinase K step. Omitting this step can result in reduced nucleic acid yield, incomplete lysis, and higher bead carryover.
FAQ-4220
I see magnetic beads in the elution plate. Is this a problem?​
Beads can be a result of high input amounts. If possible, reduce the amount of sample. To proceed with the eluate, place the samples on a magnetic rack and remove the cleared supernatant.
FAQ-4221
Can I quantify my eluates with UV-vis quantification?​
The QIAsprint Pathogen workflow uses carrier RNA to improve nucleic acid recovery, especially at low target concentrations. Carrier RNA strongly absorbs at 260 nm and therefore affects UV-vis quantification. As a result, UV-vis measurements do not reflect the true amount of pathogenic nucleic acid in the sample. For accurate quantification, functional readouts (e.g., amplifications methods) are recommended.
FAQ-4222
I have difficult-to-lyse bacteria. Which disruption methods are available?​
The QIAsprint Pathogen application offers the usage of the Pathogen Lysis Tubes (S/L) or the PowerBeadPro Tubes or Plates for efficient sample disruption. For more details see the QIAsprint Pathogen Application Guide.
FAQ-4223
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