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QIAmini DNA Tissue/Cells Kit

Automated cartridge-based purification of genomic DNA from tissue and cell samples

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QIAmini DNA Tissue/Cells (48) Kit

Cat no. / ID.   591005

48 QIAmini DNA Tissue/Cells Cartridges, 12 QIAmini Rod Covers, 2x7 mL RNase-free water, 14 mL Buffer ATL, 6 mL Buffer VXL, 1 mL Reagent DX, and 2 mL Proteinase K.
€285.00
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The QIAmini DNA Tissue/Cells Kit is intended for use with the QIAmini instrument and QIAmini protocols only. The QIAmini DNA Tissue/Cells 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 tissue, cell or buccal swab samples at a time
  • Magnetic-bead-based purification with prefilled reagents for easy handling
  • Reproducible DNA with flexible lysis options
  • Minimal hands-on time workflow: Prepare. Load. Press Start
  • Reproducible DNA purification for downstream qPCR, dPCR, NGS and other applications

Product Details

The QIAmini DNA Tissue/Cells (48) Kit contais reagents and single-use prefilled cartridges for the purification of genomic DNA from tissue samples, cultured cells or buccal swabs using QIAmini. This simple protocol is manual lysis followed by hands-free, magnetic-bead-based purification. Following lysis and Proteinase K digestion, you transfer the lysate into the prefilled cartridge, load 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 Tissue/Cells Kit is designed for laboratories looking for easy-to-use, walk-away and standardized DNA purifications for research.

Performance

The QIAmini DNA Tissue/Cells Kit together with QIAmini purifies high-yield DNA from tissue samples (such as brain, liver or spleen), cultured cells (such as Jurkat cells) or buccal swabs. The DNA yields for various tissues purified by QIAmini workflow are similar to platforms from an alternative suppliers and trusted manual spin column kits  Comparable DNA yield from fresh and frozen tissue samples. Performance of DNA from tissues was similar in qPCR  Comparable qPCR amplification from fresh and frozen tissue samples, and performance was slightly better than an alternative supplier in dPCR experiments  Comparable dPCR amplification from tissue samples.

DNA purified from cells using the QIAmini DNA Tissue/Cells Kit had higher yield and performance in qPCR and dPCR when compared to an alternate supplier, and similar yield and performance to a trusted manual spin column kit  Comparable DNA yield, qPCR amplification and dPCR performance from cultured cells.

Finally, QIAmini DNA Tissue/Cells Kit greatly reduces the hands-on time spent performing purifications compared to manual extraction method and processing times for DNA extractions on QIAmini were similar to those of an alternative supplier  Processing time comparison to the QIAmini DNA Tissue/Cells Kit.

Principle

The QIAmini DNA Tissue/Cells (48) Kit uses magnetic-bead technology for automated purification of genomic DNA from lysed tissue, cells or buccal swabs. Based on the material, samples are homogenied and lysed before loading into the prefilled cartridge. The prefilled reagent cartridge (with frame) is put in QIAmini. After the protocol is selected, QIAmini automatically performs nucleic acid binding to magnetic beads, wash steps, integrated RNA digestion and elution. The elution volume depends on the sample material used, for tissue and cell samples it is 200 µL and for low biomass samples such as buccal swabs, 60 µL. This cartridge-based protocol 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 Tissue/Cells workflow:

  1. Prepare samples by lysing tissue, cells or buccal swabs in Buffer ATL followed by Proteinase K digestion. Depending on the sample material, mechanical disruption and homogenization may be recommended.
  2. Transfer the lysate together with binding buffer VXL into the prefilled cartridge in well 1 and add elution buffer to well 5.
  3. Load the cartridge onto the QIAmini workdeck and start the protocol.*
  4. QIAmini performs binding and washing as well as elution of genomic DNA. RNA digestion is optional and be performed off-board.
  5. Recover purified DNA from the elution well to a clean tube.

*Protocols must be uploaded to the QIAmini before usage. This is a simple one-time procedure using the barcode scanner, a USB drive or a mobile device with Bluetooth. For a comprehensive list of available protocols see QIAmini Suite.

Applications

DNA purified using the QIAmini DNA Tissue/Cells 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 typeTissue, cells, buccal swabs
Sample amountUp to 50 mg (fresh, frozen) or up to 25 mg (stabilized) tissue or up to 5 x 106 cells or 1 buccal swab.
TechnologyMagnetic-particle technology
Workflow FormatPrefilled cartridge-based workflow
ProcessingAutomated on QIAmini
Elution volumeVariable, depending on sample types: 60 µL or 200 µL recommended

Resources

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
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 the DNA will be suitable for downstream assays. However, this may lead to shearing of very long DNA fragments.
FAQ-4246
How much tissue can I use?
Up to 50 mg of fresh frozen and up to 25 mg of stabilized tissue can be used. For DNA-rich tissues like spleen starting amounts should not exceed 10 mg and 5 mg, respectively.
FAQ-4247
I see some beads in my elution plate. 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 optimal lysis. To continue with the eluate, place the samples on a magnet rack and remove the cleared supernatant.
FAQ-4248
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
Which protocol should I choose?
For tissue and cell samples, the protocol option with a 200 µL elution volume is recommended for efficient DNA recovery. For low-biomass samples such as buccal swabs, the respective protocol with a lower elution volume is recommended.
FAQ-4249
How many buccal swab samples can be processed with the QIAmini DNA Tissue/Cells Kit?
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 will be sufficient for processing 30 buccal swab samples.
FAQ-4250
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
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
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
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 the DNA will be suitable for downstream assays. However, this may lead to shearing of very long DNA fragments.
FAQ-4297
How much tissue can I use?
Up to 50 mg of fresh frozen and up to 25 mg of stabilized tissue can be used. For DNA-rich tissues like spleen starting amounts should not exceed 10 mg and 5 mg, respectively.
FAQ-4298
I see some beads in my elution plate. 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 optimal lysis. To continue with the eluate, place the samples on a magnet rack and remove the cleared supernatant.
FAQ-4299
Which protocol should I choose?
For tissue and cell samples, the protocol option with a 200 µL elution volume is recommended for efficient DNA recovery. For low-biomass samples such as buccal swabs, the respective protocol with a lower elution volume is recommended.
FAQ-4300
How many buccal swab samples can be processed with the QIAmini DNA Tissue/Cells Kit?
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 will be sufficient for processing 30 buccal swab samples.
FAQ-4301