QIAsprint modular system: Magnetic bead DNA extraction from blood

For automated purification of genomic DNA, from up to 200 μL of blood samples, for all downstream applications

S_1084_5_GEN_V2

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QIAsprint DNA Blood PrepSet (384)

Cat no. / ID.   585459

Buffer AL, Proteinase K, and Buffer RDW for 384 DNA preparations from blood samples
Kit
PrepSet
Essential Kit
Add on
QIAsprint Consumables
The QIAsprint DNA Blood PrepSet (384) is intended for molecular biology applications. This product is not intended for the diagnosis, prevention, or treatment of a disease.
QIAsprint modular system: Magnetic bead DNA extraction from blood 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

  • Eliminate manual lysis through complete digestion using Buffer AL and Proteinase K to reduce hands-on time  
  • Reduce user interaction with fully automated processing after run initiation
  • Simplify protocol adaptation for diverse blood workflows using modular Essential Kits and PrepSets
  • Minimize logistical overhead with reagents shipped at ambient temperature to simplify storage

Product Details

The QIAsprint modular kit system is a high-throughput solution for genomic DNA isolation from blood. It combines flexible modular architecture with automated magnetic bead purification, allowing fully automated processing on the QIAsprint Connect system without manual intervention. 

For 384-well blood genomic DNA isolation, the system utilizes two primary reagent modules: 

  • QIAsprint DNA Blood PrepSet (384): Optimized for sample pretreatment, this module provides Buffer AL for cell lysis and Proteinase K for thorough protein digestion.
  • QIAsprint Essential Kit A (384): This module provides the paramagnetic particles and wash buffers required for DNA purification, ensuring high yield, reproducibility and recovery of high-quality DNA.

This platform is optimized for the automated processing of up to 384 samples, ensuring no hands-on time and reproducible performance for diverse research workflows.

Performance

The QIAsprint DNA Blood workflow enables efficient purification of high-molecular-weight genomic DNA from whole blood across a range of input volumes. Using the QIAsprint DNA Blood PrepSet together with Essential Kit A on the QIAsprint Connect, consistent DNA recovery is achieved from 50–300 µL blood samples with reproducible performance across replicates (see  DNA recovery from whole blood at increasing input volumes). The purified DNA provides reliable yield and quality suitable for downstream analyses such as qPCR and other molecular biology applications. 

In internal comparisons with alternative automated magnetic bead workflows, the QIAsprint DNA Blood workflow demonstrated competitive DNA recovery and strong amplification performance, supporting its use in demanding high-throughput laboratory environments (see  Comparative evaluation of DNA yield and qPCR amplification from blood sample).

Principle

The QIAsprint DNA Blood workflow uses a modular approach for efficient and flexible DNA purification on the QIAsprint Connect system. Sample pretreatment is performed with the QIAsprint DNA Blood PrepSet (384), where Buffer AL and Proteinase K digestion enable complete lysis of blood samples. The QIAsprint Essential Kit A (384) then provides the magnetic beads and buffers required for the automated bind–wash–elute steps. During processing, DNA binds to magnetic beads, contaminants are washed away and high-quality DNA is eluted for downstream analysis. 

If the workflow needs to be adapted for other applications, the QIAsprint modular kit system allows the DNA Blood PrepSet to be combined with other compatible Essential Kits. In addition, nearly all buffers and reagents used in the system are available as standalone items, providing further customization options for specialized workflows (see QIAsprint sets and consumables finder). 

Procedure

The QIAsprint blood DNA workflow supports straightforward pretreatment and an automated purification process that requires zero manual intervention once the run starts (see  QIAsprint DNA blood workflow).

Standard protocol steps: 

  • Sample lysis and digestion: Proteinase K is mixed with the blood sample and Buffer AL to enable enzymatic digestion and complete lysis.
  • DNA binding: The lysate is combined with MagG Bead Suspension and isopropanol to promote efficient binding of DNA to the magnetic beads.
  • Plate preparation: Wash plates and the elution plate are prepared according to the protocol and placed into the plate hotels.
  • Automated purification: Plate hotels are loaded onto the QIAsprint Connect instrument and the selected protocol performs automated magnetic bead–based bind, wash and elute steps.

Applications

DNA purified with the QIAsprint DNA Blood 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 between protocols, 100 µL default
Main sample typeBlood
ProcessingAutomated on QIAsprint
AnalyteGenomic DNA
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 (3)
Highly pure, nuclease-free water for use in all molecular biology applications
Buffer AL - (EN)
PDF (87.8KB)
Download
for DNA isolation using QIAamp and DNeasy Kits
Protocols (1)
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
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
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 yields. What can I do?
Thorough lysis is crucial for a good DNA recovery. Ensure that samples are mixed properly after addition of Buffer AL.
FAQ-4239
How much blood can I use?
The protocol is optimized for 200 µL of blood but can be adjusted to a maximum 300 µL per binding plate. The QIAsprint Connect instrument allows protocol adjustment to meet application-specific needs. If processing larger blood volumes are required,  a subsequent binding using the same beads can be implemented. 
FAQ-4240
May I skip the Proteinase K step?
Omitting the Proteinase K step may result in reduced DNA yield and  possible bead carryover in the eluate. 
FAQ-4241
I see beads in my elution plate. Is this a problem, and what can I do?
Beads can result from high input amounts. If possible, reduce the sample input and ensure that Proteinase K was used. To proceed with the eluate, place the samples on a magnetic rack and remove the cleared supernatant.
FAQ-4242
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