QIAamp RNA Blood Mini Kit – RNA Extraction from Blood

For purification of cellular RNA from fresh whole blood

S_1622_RPA_QA_1065

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QIAamp RNA Blood Mini Kit (50)

Cat no. / ID.   52304

For 50 RNA preps: 50 QIAamp Mini Spin Columns, 50 QIAshredder Spin Columns, Collection Tubes (1.5 ml and 2 ml), RNase-free reagents and buffers
€445.00
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KitBuffer
QIAamp RNA Blood Mini Kit
Buffer AW1
The QIAamp RNA Blood Mini Kit 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

  • Rapid purification of high-quality, ready-to-use RNA
  • No organic extraction or alcohol precipitation
  • Consistent, high yields
  • Removal of contaminants and inhibitors

Product Details

The QIAamp RNA Blood Mini Kit provides silica-membrane-based purification of cellular RNA from up to 1.5 ml of fresh, whole human blood stabilized with any common anticoagulant, such as citrate, heparin, or EDTA. After homogenization using the QIAshredder spin column, a fast spin-column procedure simplifies RNA purification. Purification can be fully automated on the QIAcube Connect.

Performance

The QIAamp procedure completely removes RNases, contaminants, and enzyme inhibitors, yielding high-quality RNA suitable for any downstream application (see figures " High-quality RNA for northern analysis" and " Reliable RT-PCR analysis").

The QIAamp RNA Blood Mini Kit provides the highest-quality RNA with minimum copurification of DNA. However, as with any RNA purification method, some DNA contamination can be expected. For certain RNA applications that are sensitive to very small amounts of DNA, it may be necessary to remove any remaining DNA. In these cases, the QIAGEN RNase-Free DNase Set provides convenient on-column DNase treatment of RNA samples during QIAamp RNA procedures.

See figures

Principle

The QIAamp RNA Blood Mini Kit provides purification of cellular RNA using silica-membrane technology. No phenol–chloroform extraction is required. RNA binds specifically to the QIAamp silica-gel membrane while contaminants pass through. PCR inhibitors, such as divalent cations and proteins, are completely removed in two efficient wash steps, leaving pure RNA to be eluted in either water or a buffer provided with the kit.

QIAamp technology yields total cellular RNA from fresh whole blood and other sample sources that is ready to use in RT-PCR and blotting procedures. QIAamp sample preparation technology is fully licensed.

Procedure

The QIAamp RNA Blood Mini Kit simplifies isolation of RNA from blood with a fast spin-column procedure (see figure " Procedure"). Red blood cells are selectively lysed and white cells collected by centrifugation. White cells are then lysed using highly denaturing conditions which immediately inactivate RNases. After homogenization using the QIAshredder spin column, the sample is applied to the QIAamp spin column. Total RNA binds to the QIAamp membrane and contaminants are washed away, leaving pure RNA to be eluted in 30–100 µl RNase-free water (provided with the kit) for direct use in any downstream application.
See figures

Applications

QIAamp RNA Blood Mini Kits provide a fast, easy method for the preparation of total cellular RNA from up to 1.5 ml of human whole blood. Contaminants and enzyme inhibitors, such as hemoglobin and heparin, are completely removed, leaving purified RNA ready for use in downstream applications, such as: 

  • RT-PCR
  • Real-time RT-PCR
  • cDNA synthesis
  • Northern, dot and slot blotting
  • RNase/S1 nuclease protection
  • Differential display
  • Poly A+ RNA selection
  • Primer extension

In addition, QIAamp RNA Blood Mini Kits can be used to purify total RNA from tissues and cultured cells and to separate RNA from proteins, salt and other reaction components after enzymatic reactions, such as DNase digestions, proteinase digestions, RNA ligation and labeling reactions. 

Supporting data and figures

Specifications

FeaturesSpecifications
applicationsPCR, real-time PCR, microarray
elutionvolume30–100 µl
mainsampletypeWhole blood, tissue
purificationoftotalrnamirnapolyamrnadnaorproteinCellular RNA
sampleamount50–1.5 ml
formatSpin columns
processingManual (centrifugation)
timeperrunorperprep<1 hour
technologySilica technology
yield1–5 µg

Resources

Kit Handbooks (1)
For total RNA purification from human whole blood
Scientific Posters (1)
Poster for download
Safety Data Sheets (1)
Download Safety Data Sheets for QIAGEN product components.
Certificates of Analysis (1)

Publications

Preanalytical mRNA stabilization of whole bone marrow samples.
Langebrake C; Günther K; Lauber J; Reinhardt D;
Clin Chem; 2007; 53 (4):587-93 2007 Feb 8 PMID:17289802
Histone acetylation dependent allelic expression imbalance of BAPX1 in patients with the oculo-auriculo-vertebral spectrum.
Fischer S; Lüdecke HJ; Wieczorek D; Böhringer S; Gillessen-Kaesbach G; Horsthemke B;
Hum Mol Genet; 2006; 15 (4):581-7 2006 Jan 11 PMID:16407370
Molecular analysis of the GNAS1 gene for the correct diagnosis of Albright hereditary osteodystrophy and pseudohypoparathyroidism.
De Sanctis L; Romagnolo D; Olivero M; Buzi F; Maghnie M; Scirè G; Crino A; Baroncelli GI; Salerno M; Di Maio S; Cappa M; Grosso S; Rigon F; Lala R; De Sanctis C; Dianzani I;
Pediatr Res; 2003; 53 (5):749-55 2003 Mar 5 PMID:12621129
Perforin-dependent brain-infiltrating cytotoxic CD8+ T lymphocytes mediate experimental cerebral malaria pathogenesis.
Nitcheu J; Bonduelle O; Combadiere C; Tefit M; Seilhean D; Mazier D; Combadiere B;
J Immunol; 2003; 170 (4):2221-8 2003 Feb 15 PMID:12574396