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QIAmini DNA Blood Kit

Automated cartridge-based purification of genomic DNA from blood samples

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QIAmini DNA Blood (48) Kit

Cat no. / ID.   590105

Prefilled cartridge-based kit for automated genomic DNA isolation from whole blood samples on QIAmini.
$263.00
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The QIAmini DNA Blood Kit is intended for use with the QIAmini instrument and QIAmini protocols only. The QIAmini DNA Blood Kit is intended for Research Use Only. Not for use in diagnostic procedures.

✓ 24/7 automatic processing of online orders

✓ Knowledgeable and professional Product & Technical Support

✓ Fast and reliable (re)-ordering

Features

  • Automated purification of genomic DNA from up to 8 whole blood samples in parallel
  • Magnetic-bead-based purification with prefilled reagents for easy handling
  • Minimal hands-on time workflow: Lyse. Load. Press Start
  • Reproducible DNA purification for downstream qPCR, dPCR, NGS and other applications

Product Details

The QIAmini DNA Blood (48) Kit contains reagents and single-use prefilled cartridges for the purification of genomic DNA from whole blood using QIAmini. This simple protocol consists of manual lysis followed by hands-free, magnetic-bead-based purification. Buffer AL and Proteinase K digestion enable complete lysis of blood samples. Following lysis, you transfer the lysate into the prefilled cartridge, loads the cartridge into the QIAmini and start the protocol. Prefilled cartridges minimize pipetting and reduce the risk of human error, leading to reproducible DNA recovery. Purified DNA is suitable for a wide range of downstream applications including qPCR, dPCR and DNA sequencing. The QIAmini DNA Blood Kit is designed for laboratories looking for easy-to-use, walk-away and standardized DNA purifications for research.

Performance

The QIAmini DNA Blood Kit together with QIAmini purifies high-yield DNA from whole blood samples (treated with EDTA, ACD, or heparin). The DNA yields are comparable to or higher than platforms and kits from alternative suppliers while having a lower overall total processing time. qPCR results also show similar Cqs for β-actin regardless of kit or automation instrument, indicating similar DNA purification quality for downstream analyses  Comparable yield and qPCR amplification using DNA from blood samples.

The DNA yield and quality is comparable whether purified by QIAmini DNA Blood Kit and or a trusted manual spin-column kit  Comparable DNA recovery from different donors.

Finally, QIAmini DNA Blood Kit greatly reduces the hands-on time spent performing purifications compared to manual extraction method and processing times for DNA extractions on QIAmini are lower or similar to those of alternative suppliers  Processing time comparison to the QIAmini DNA Blood Kit. 

Principle

The QIAmini DNA Blood (48) Kit uses magnetic-bead technology for automated purification of genomic DNA from whole blood. Enzymatic digestion and complete lysis easily achieved through mixing the blood samples with Proteinase K and Buffer AL. The lysate is then loaded into the prefilled cartridge where it is combined with the magnetic beads and isopropanol. The cartridge is prepared and put (with frame) in QIAmini. After the protocol is selected, QIAmini automatically performs nucleic acid binding to magnetic beads, wash steps, and elution.

The recommended elution volume is 100 µL, however adjustable are typically in a range of 50-200 µL. This cartridge-based workflow simplifies reagent handling and reduces manual pipetting during nucleic acid purification. The purified DNA can be either used immediately in downstream applications or stored for future use.

Procedure

The simple and intuitive protocol requires only a few preparation and loading steps before fully automated purification begins  QIAmini DNA Blood Kit workflow:

  1. Prepare samples homogenization and lysis with Proteinase K followed by buffer AL. Vortexing or efficient pipetting the mix ensures a consistent lysis.
  2. Transfer the lysate into the prefilled cartridge in well 1 and add RNase-free water to well 5.
  3. Load the cartridge onto the QIAmini workdeck and start the protocol.*
  4. QIAmini performs binding, washing, and elution of genomic DNA.
  5. Recover purified DNA from the elution well to a clean tube.

Applications

DNA purified using the QIAmini DNA blood Kit can be used in downstream applications including:

  • Quantitative PCR (qPCR)
  • Digital PCR (dPCR)
  • NGS
  • long-read sequencing

Supporting data and figures

Specifications

FeaturesSpecifications
ApplicationsAutomated purification of genomic DNA on QIAmini
Main sample typeWhole blood
Sample amountUp to 200 µL
TechnologyMagnetic-particle technology
ProcessingAutomated on QIAmini
Elution volumeRecommended elution volume 100 µL. Typically adjustable between 50 and 200 µL.

Resources

Kit Handbooks & Protocols (3)
Safety Data Sheets (1)
Download Safety Data Sheets for QIAGEN product components.
Certificates of Analysis (1)
Software-related downloads (2)
QIAmini Suite
LITERATURE (17.7KB)
Browse and transfer protocols, manage reports, access protocol guidance and troubleshooting resources.
All QIAmini protocol scripts for download and transfer to the instrument via USB drive.
User Manuals (1)

FAQ

I see magnetic beads in the elution well. Is this a problem?​
Beads can result from high sample input amounts. If possible, reduce the amount of sample. To proceed with the eluate, place the samples on a magnet rack and remove the cleared supernatant.
FAQ-4243
What do I need to do after the QIAmini run is completed?
After removing and discarding the rod cover(s), remove the cartridge frame holding the cartridge(s) and transfer the purified nucleic acids into a new reaction tube (e.g., a 1.5 mL tube). 
FAQ-4244
I see reagent splashing, droplets on top of the cartridge wells, or plastic fragments remaining after removing the seal. What should I do?
Before removing the sealing film, invert the prefilled cartridge to resuspend the magnetic beads and gently flick it to collect the reagents and bead suspension at the bottom of the wells. Carefully peel off the sealing film to avoid splashing, inspect the cartridge rim and remove any remaining pieces or thin strands of sealing material before loading the cartridge into the instrument.
FAQ-4241
When resuspending my cell pellet, the sample becomes very viscous. What can I do?
For high cell numbers and/or certain cell lines, this may happen at >1 × 10⁶ cells. Using homogenization methods like the TissueLyser III, Tissue Ruptor II, a vortex with the appropriate adapter or passing the sample through a needle will help.
FAQ-4245
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-4253
Can I vary the elution volume​?
The default elution volume is 80 µL, but it can be adjusted. The range is 50–200 µL.
FAQ-4255
I see some beads in my elution well. Is this a problem? What can I do?
Residual beads can result from high sample input amounts. If possible, reduce the amount of sample. Make sure Proteinase K has been used for optimized lysis. To continue with the eluate, place the samples on a magnet rack and remove the cleared supernatant.
FAQ-4254
How can I prevent reagent loss when removing the cartridge seal?
After inverting the reagent cartridge to resuspend the magnetic particles, gently flick the cartridge to collect the reagents at the bottom of each well before removing the seal. This reduces the risk of reagent loss during seal removal.
FAQ-4242
Can I run chemistry from other vendors on the QIAmini?​
No, the QIAmini is a closed system using prefilled cartridges and QIAGEN-validated protocols.
The plastics that fit the instrument can only be ordered from QIAGEN. The instrument will not physically accept plastics from similar systems.
FAQ-4238
Can I change all parameters of my QIAmini protocol?
It is possible to adjust some parameters such as temperature, incubation time, and elution volume.
FAQ-4239
I get low yields. What can I do?
Thorough lysis is crucial for a good DNA recovery. Ensure that samples are mixed properly after the addition of Buffer AL.
FAQ-4251
The required protocol to run my kit on the QIAmini is not installed on my instrument. How can I obtain it?
Download the appropriate protocol file from www.qiagen.com/QIAmini or from QIAmini Suite (www.qiagen.com/QIAminiSuite). The protocols can be adapted to suit experimental setup needs via QIAmini Suite and transferred to the instrument via a USB drive, Bluetooth or QIAmini barcode scanner. The instrument’s touchscreen display allows the user to easily select and start protocols. 
FAQ-4240
How much blood can I use?
The protocol is designed for 200 µL of blood.
FAQ-4252
Can I run chemistry from other vendors on the QIAmini?​
No, the QIAmini is a closed system using prefilled cartridges and QIAGEN-validated protocols.
The plastics that fit the instrument can only be ordered from QIAGEN. The instrument will not physically accept plastics from similar systems.
FAQ-4289
Can I change all parameters of my QIAmini protocol?
It is possible to adjust some parameters such as temperature, incubation time, and elution volume.
FAQ-4290
The required protocol to run my kit on the QIAmini is not installed on my instrument. How can I obtain it?
Download the appropriate protocol file from www.qiagen.com/QIAmini or from QIAmini Suite (www.qiagen.com/QIAminiSuite). The protocols can be adapted to suit experimental setup needs via QIAmini Suite and transferred to the instrument via a USB drive, Bluetooth or QIAmini barcode scanner. The instrument’s touchscreen display allows the user to easily select and start protocols. 
FAQ-4291
I see reagent splashing, droplets on top of the cartridge wells, or plastic fragments remaining after removing the seal. What should I do?
Before removing the sealing film, invert the prefilled cartridge to resuspend the magnetic beads and gently flick it to collect the reagents and bead suspension at the bottom of the wells. Carefully peel off the sealing film to avoid splashing, inspect the cartridge rim and remove any remaining pieces or thin strands of sealing material before loading the cartridge into the instrument.
FAQ-4292
How can I prevent reagent loss when removing the cartridge seal?
After inverting the reagent cartridge to resuspend the magnetic particles, gently flick the cartridge to collect the reagents at the bottom of each well before removing the seal. This reduces the risk of reagent loss during seal removal.
FAQ-4293
I see magnetic beads in the elution well. Is this a problem?​
Beads can result from high sample input amounts. If possible, reduce the amount of sample. To proceed with the eluate, place the samples on a magnet rack and remove the cleared supernatant.
FAQ-4294
What do I need to do after the QIAmini run is completed?
After removing and discarding the rod cover(s), remove the cartridge frame holding the cartridge(s) and transfer the purified nucleic acids into a new reaction tube (e.g., a 1.5 mL tube). 
FAQ-4295
When resuspending my cell pellet, the sample becomes very viscous. What can I do?
For high cell numbers and/or certain cell lines, this may happen at >1 × 10⁶ cells. Using homogenization methods like the TissueLyser III, Tissue Ruptor II, a vortex with the appropriate adapter or passing the sample through a needle will help.
FAQ-4296
I get low yields. What can I do?
Thorough lysis is crucial for a good DNA recovery. Ensure that samples are mixed properly after the addition of Buffer AL.
FAQ-4302
How much blood can I use?
The protocol is designed for 200 µL of blood.
FAQ-4303
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-4304
I see some beads in my elution well. Is this a problem? What can I do?
Residual beads can result from high sample input amounts. If possible, reduce the amount of sample. Make sure Proteinase K has been used for optimized lysis. To continue with the eluate, place the samples on a magnet rack and remove the cleared supernatant.
FAQ-4305
Can I vary the elution volume​?
The default elution volume is 80 µL, but it can be adjusted. The range is 50–200 µL.
FAQ-4306