AllPrep DNA/RNA Kits

For simultaneous purification of DNA and RNA from cells and tissues, including small samples, in spin-column and 96-well format

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AllPrep DNA/RNA Mini Kit (50)

Cat no. / ID.   80204

For 50 minipreps: AllPrep DNA Spin Columns, RNeasy Mini Spin Columns, Collection Tubes, RNase-Free Water and Buffers 
US$797.00
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Kit
AllPrep DNA/RNA Kit
Eco-friendlier kit
Column typePlate type
Mini
Micro
96 well
For information on storage and stability, see the relevant kit handbook, instructions for use or instrument user manual under the Resources tab
The AllPrep DNA/RNA Kits is intended for molecular biology applications. This product is not intended for the diagnosis, prevention, or treatment of a disease.
Is sustainability important to you?
For an eco-friendlier alternative to the selected product, look no further.

Features

  • High-quality DNA and RNA from the same sample
  • Maximal yields of DNA and RNA from precious samples
  • Rapid purification with short, streamlined protocol
  • Streamlined protocols for 96-well plates
  • Ready-to-use DNA and RNA for any downstream analysis

Product Details

AllPrep DNA/RNA Kits enable simultaneous purification of genomic DNA and total RNA from each cell or tissue sample. Since there is no need to divide each sample into two for separate purification procedures, maximum yields of DNA and RNA can be achieved. The purified DNA and RNA are eluted separately.

The AllPrep DNA/RNA Micro and Mini Kits can be automated on the QIAcube Connect. The AllPrep DNA/RNA 96 Kit is well suited for high-throughput purification of genomic DNA and total RNA from up to 96 samples.

 

Performance

Small samples of cultured cells and easy-to-lyse tissues can be processed with AllPrep DNA/RNA technology (see table “Optimal yields of DNA and RNA from tissues using the AllPrep DNA/RNA Micro Kit”). Genomic DNA is purified using the novel AllPrep DNA spin column, and total RNA is purified using an RNeasy MinElute spin column. Total RNA with Agilent RIN values of close to 10 is routinely obtained from cultured cells. Genomic DNA and total RNA show reliable quantification over a wide dynamic range (see figure " Wide dynamic range").

Optimal yields of DNA and RNA from tissues using the AllPrep DNA/RNA Micro Kit

Tissue (5 mg) DNA yield (µg)* RNA yield (µg)*
Heart 3.89 2.00
Brain 2.60 3.08
Kidney 11.33 12.70
Liver 32.40 16.02
Lung 9.65 24.63
Spleen 20.50 43.51
Thymus 34.90 56.89
Intestine 26.71 27.38

A simple workflow allows DNA and RNA extraction from one sample. The purified genomic DNA has an average length of 15–30 kb and performs well in multiplex PCR (see figure  "Multiplex PCR of 8 targets"). Total RNA is of high quality and has a RIN value of 10 indicating that the RNA is intact (see figure " Simultaneous purification of total RNA and genomic DNA" and figure " High-quality total RNA").

AllPrep DNA/RNA technology also enables efficient purification of high-quality DNA and RNA from different cell and tissue types in convenient 96-well format (see table “High-quality RNA from tissues purified using the AllPrep DNA/RNA 96 Kit” and figure " Reproducible purification of DNA and RNA in 96-well format").

High-quality RNA from tissues purified using the AllPrep DNA/RNA 96 Kit

Rat tissue RIN value*
Liver 9.4
Lung 9.5
Spleen 9.6
Thymus 10.0

There is no need for additional RNase or DNase digestion (see figure " RNA with no genomic DNA contamination") and the purified DNA is suitable for downstream applications (see figure " High-quality DNA for reliable multiplex PCR analysis").

See figures

Principle

AllPrep DNA/RNA Kits are designed to purify both genomic DNA and total RNA from the same cell or tissue sample. Since there is no need to divide the sample into two for separate purification procedures, maximum yields of DNA and RNA can be achieved. Efficient purification of high-quality DNA and RNA from different tissue types is achieved without the need for additional RNase or DNase digestion. The purified DNA and RNA are eluted separately and ready to use in any downstream application. Processing in 96-well format makes AllPrep DNA/RNA technology the ideal tool for sample preparation in genomics and systems biology.

For a more sustainable alternative, we have the QIAwave DNA/RNA Mini Kit. This kit reduces plastic and cardboard usage by up to 52% and 58%, respectively compared to the AllPrep DNA/RNA Mini Kit. It features waste tubes made from 100% recycled plastic, which can be reused throughout the procedure. The QIAwave buffers, in concentrated form, cut down plastic consumption by up to 90% per bottle. Despite the visual difference, the QIAwave Kit maintains user-friendliness with chemistry and performance identical to the standard kit.

In partnership with My Green Lab, we've also assessed the environmental impact of the AllPrep DNA/RNA Mini Kit (50) and the QIAwave DNA/RNA Mini Kit (50). My Green Lab ACT environmental impact factor labels aim to assess and rate products based on various sustainability criteria, including: 

  • Manufacturing
  • Responsible chemical management 
  • Sustainable content within products and packaging materials
  • Disposal of the packaging at the end of life 


Products are scored from 1 to 10 except for energy and water consumption, which are scored as 1 point per kWh or gallon, respectively. A low score means a lower environmental impact (see figures "DNA/RNA Mini Kits (50) environmental impact factor label    US,   EU and   UK").

See figures

Procedure

A simple spin-column workflow allows the purification of high-quality DNA and RNA from the same sample (see flowchart “ AllPrep DNA/RNA procedure”). Both cultured cells and easy-to-lyse tissues can be processed. Genomic DNA is purified using the novel AllPrep DNA spin column, and total RNA is purified using an RNeasy Mini or RNeasy MinElute spin column (AllPrep DNA/RNA Micro Kit).

When disrupting and homogenizing tissues in Buffer RLT Plus (supplied with the AllPrep DNA/RNA Micro Kit and Allprep DNA/RNA Mini Kit), excessive foaming may occur (please note this is not the case for the Allprep DNA/RNA 96 Kit since this product is supplied with Buffer RLT). This foaming is substantially reduced by adding Reagent DX (supplied separately) to Buffer RLT Plus at a final concentration of 0.5% (v/v) before starting disruption and homogenization. Reagent DX has been carefully tested with the kits, and has no effect on RNA purity or on downstream applications such as real-time RT-PCR. Buffer RLT Plus containing Reagent DX can be stored at room temperature (15–25ºC) for at least 9 months.

A supplementary protocol allows optional purification of protein. For experiments where DNA, RNA, and protein are regularly prepared from each sample, the AllPrep DNA/RNA/Protein Mini Kit can be used instead.

For high-throughput processing, the 96-well purification plates of the AllPrep DNA/RNA 96 Kit are for both DNA and RNA. The plates are rapidly and conveniently processed using either a centrifuge (Centrifuge 4-16 and Plate Rotor 2 x 96) or a combination of vacuum (QIAvac 96) and centrifuge. Both cultured cells and easy-to-lyse tissues can be processed.

AllPrep DNA/RNA Kits form part of QIAGEN's solution for preparing multiple analytes from the same sample. These include Allprotect Tissue Reagent, which stabilizes DNA, RNA, and protein in tissues, and RNAprotect Cell Reagent, which stabilizes DNA and RNA in cells. Both reagents deliver immediate stabilization at room temperature. For tissues, TissueRuptor and TissueLyser systems provide fast disruption at low- to high-throughputs.

See figures

Applications

The purified genomic DNA has an average length of 15–30 kb, depending on homogenization conditions, and is suited for any application, including next-generation sequencing, Southern-, dot-, and slot-blot analyses; and PCR and multiplex PCR.

The purified total RNA can be used in any application, such as RNA-seq RT-PCR and real-time RT-PCR; differential display; cDNA synthesis; northern-, dot-, and slot-blot analyses; and microarrays.

A supplementary protocol allows optional purification of protein. The purified protein is denatured and can be used in applications such as SDS-PAGE, western blotting, and 2D gel electrophoresis.

Comparison of AllPrep DNA/RNA Kits

Features AllPrep DNA/RNA Micro Kit AllPrep DNA/RNA Mini Kit AllPrep DNA/RNA 96 Kit
Applications PCR, RT-PCR, real-time PCR,
cDNA synthesis, microarray, blotting
PCR, real-time PCR, microarray,
blotting
PCR, real-time PCR, microarray,
blotting
Elution volume DNA: 30 µl; RNA: 10 µl 100 µl 50–100 µl
Format Spin column Spin column 96-well plate
Main sample type Cells, tissue Cells, tissue Cultured cells, easy-to-lyse tissue
Processing Manual (centrifugation) Manual (centrifugation) Manual (centrifugation and/or vacuum)
Purification of total RNA, miRNA,
poly A+ mRNA, DNA or protein
Genomic DNA and total RNA Genomic DNA and total RNA Total RNA, DNA, miRNA (optional)
Sample amount 5 x 105 cells or 5 mg tissue 1 x 107 cells or 30 mg tissue Up to 2 x 106 cells/up to 10 mg tissue
Technology Silica technology Silica technology Silica technology
Time per run or per prep 35 min 35 min 60 min
Yield Varies Varies Varies

Supporting data and figures

Resources

Kit Handbooks (3)
For simultaneous purification of genomic DNA and total RNA from the same small sample, including
  • animal and human cells (≤5 x 10^5)
  • animal and human tissues (≤5 mg)
  • microdissected cryosections
For simultaneous purification of genomic DNA and total RNA from animal and human cells and tissues in 96-well format
Brochures & Guides (1)
Safety Data Sheets (1)
Download Safety Data Sheets for QIAGEN product components.
Certificates of Analysis (1)

Publications

Simultaneous targeting of TGF-β/PD-L1 synergizes with radiotherapy by reprogramming the tumor microenvironment to overcome immune evasion.
Lan Y; Moustafa M; Knoll M; Xu C; Furkel J; Lazorchak A; Yeung TL; Hasheminasab SM; Jenkins MH; Meister S; Yu H; Schlegel J; Marelli B; Tang Z; Qin G; Klein C; Qi J; Zhou C; Locke G; Krunic D; Derner MG; Schwager C; Fontana RE; Kriegsmann K; Jiang F; Rein K; Kriegsmann M; Debus J; Lo KM; Abdollahi A;
Cancer Cell; 2021; 39 (10):1388-1403.e10 2021 Sep 9 PMID:34506739
Anti-PD-1/L1 lead-in before MAPK inhibitor combination maximizes antitumor immunity and efficacy.
Wang Y; Liu S; Yang Z; Algazi AP; Lomeli SH; Wang Y; Othus M; Hong A; Wang X; Randolph CE; Jones AM; Bosenberg MW; Byrum SD; Tackett AJ; Lopez H; Yates C; Solit DB; Ribas A; Piva M; Moriceau G; Lo RS;
Cancer Cell; 2021; 39 (10):1375-1387.e6 2021 Aug 19 PMID:34416167
NTRK Fusion Genes in Thyroid Carcinomas: Clinicopathological Characteristics and Their Impacts on Prognosis.
Pekova B; Sykorova V; Mastnikova K; Vaclavikova E; Moravcova J; Vlcek P; Lastuvka P; Taudy M; Katra R; Bavor P; Kodetova D; Chovanec M; Drozenova J; Astl J; Hrabal P; Vcelak J; Bendlova B;
Cancers (Basel); 2021; 13 (8) 2021 Apr 16 PMID:33923728
Engineered virus-like particles for transient delivery of prime editor ribonucleoprotein complexes in vivo.
An M; Raguram A; Du SW; Banskota S; Davis JR; Newby GA; Chen PZ; Palczewski K; Liu DR;
Nat Biotechnol; 2024; 42 (10):1526-1537 2024 Jan 8 PMID:38191664
Engineered virus-like particles for efficient in vivo delivery of therapeutic proteins.
Banskota S; Raguram A; Suh S; Du SW; Davis JR; Choi EH; Wang X; Nielsen SC; Newby GA; Randolph PB; Osborn MJ; Musunuru K; Palczewski K; Liu DR;
Cell; 2022; 185 (2):250-265.e16 2022 Jan 11 PMID:35021064