QIAquick 96 PCR Purification Kits – DNA Cleanup

For purification of 96 PCR products (up to 10 µg), 100 bp to 10 kb

S_1346_DNA_QQ0827

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QIAquick 96 PCR Purification Kit (4)

Cat no. / ID.   28181

For purification of 4 x 96 PCR reactions: 4 QIAquick 96 Plates, Buffers, Collection Microtubes (1.2 ml), Caps
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Kit
QIAquick 96 PCR Purification Kit
QIAquick 96 PCR BioRobot Kit
Preparations
4
24
QIAquick 96 PCR Purification Kits 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

  • Up to 95% recovery of ready-to-use DNA
  • Fast and convenient procedure
  • Cleanup of DNA up to 10 kb in three easy steps

Product Details

QIAquick 96 PCR Purification Kits provide 96-well plates, buffers, and collection tubes for high-throughput silica-membrane-based purification of PCR products >100 bp in size. DNA up to 10 kb is purified using a simple and fast bind–wash–elute procedure and an elution volume of 60–80 µl (resulting in an eluate volume of 40–60 µl). The cleanup procedure can be fully automated on the BioRobot Universal workstation using the QIAquick 96 PCR BioRobot Kit.

Performance

The QIAquick 96 PCR Kit provides a quick and easy method for high-throughput purification of PCR samples, with a recovery rate of up to 90%. The QIAquick 96 procedure delivers highly pure DNA suitable for various downstream applications (see figure " Accurate sequencing"). Using the QIAvac 96, DNA fragments 100 bp – 10 kb in size are purified from 1–4 x 96 samples.
See figures

Principle

QIAquick 96 Kits contain a silica-membrane assembly for binding of DNA in high-salt buffer and elution with low-salt buffer or water. The purification procedure removes primers, nucleotides, enzymes, mineral oil, salts, agarose, ethidium bromide, and other impurities from DNA samples. Silica-membrane technology eliminates the problems and inconvenience associated with loose resins and slurries. Specialized binding buffers are optimized for specific applications and promote selective adsorption of DNA molecules within particular size ranges.

The QIAquick 96 procedure allows parallel purification of up to 96 PCR samples using efficient vacuum-driven purification on a QIAvac 96.
The QIAquick 96 PCR BioRobot Kit is a special kit format optimized for use on the BioRobot Universal. The kit provides QIAquick 96 modules, together with all buffers and plasticware required for automated high-throughput cleanup of 96 PCR samples.

Procedure

The QIAquick system uses a simple bind–wash–elute procedure (see flowchart " QIAquick 96 procedure"). Binding buffer is added directly to the PCR sample or other enzymatic reaction, and the mixture is applied to the 96-well plate. Nucleic acids adsorb to the silica membrane in the high-salt conditions provided by the buffer. Impurities are washed away and pure DNA is eluted with a small volume of low-salt buffer provided or water, ready to use in subsequent applications.

Handling

QIAquick multiwell modules are processed using vacuum-driven purification on QIAvac manifolds. The QIAquick 96 PCR Purification Kit requires the use of the QIAvac 96 vacuum manifold. The cleanup procedure can be fully automated on the BioRobot Uworkstations using the QIAquick 96 PCR BioRobot Kit.

See figures

Applications

DNA fragments purified with the MinElute or QIAquick system are ready for direct use in many applications, including sequencing, microarray analysis, ligation and transformation, restriction digestion, labeling, microinjection, PCR, and in vitro transcription.

Supporting data and figures

Specifications

FeaturesSpecifications
bindingcapacity10 µg
processingManual/automated
removal10mers1740mersdyeterminatorproteinsRemoval <40mers
sampletypeapplicationsDNA, oligonucleotides: PCR reactions
format96-well plate
fragmentsize100 bp – 10 kb
technologySilica technology
recoveryoligonucleotidesdsdnaRecovery: oligonucleotides, dsDNA
elutionvolume60–80 µl

Resources

Quick-Start Protocols (1)
Kit Handbooks (1)
For rapid purification of multiple PCR products 
Safety Data Sheets (1)
Download Safety Data Sheets for QIAGEN product components.
Certificates of Analysis (1)

Publications

Temporal and differential gene expression of Singapore grouper iridovirus.
Chen LM; Wang F; Song W; Hew CL;
J Gen Virol; 2006; 87 (Pt 10):2907-2915 2006 Oct PMID:16963749
Comparative genomics of host-specific virulence in Pseudomonas syringae.
Sarkar SF; Gordon JS; Martin GB; Guttman DS;
Genetics; 2006; 174 (2):1041-56 2006 Sep 1 PMID:16951068
cDNA microarrays as a tool for identification of biomineralization proteins in the coccolithophorid Emiliania huxleyi (Haptophyta).
Quinn P; Bowers RM; Zhang X; Wahlund TM; Fanelli MA; Olszova D; Read BA;
Appl Environ Microbiol; 2006; 72 (8):5512-26 2006 Aug PMID:16885305
Characterization of the vernalization response in Lolium perenne by a cDNA microarray approach.
Ciannamea S; Busscher-Lange J; de Folter S; Angenent GC; Immink RG;
Plant Cell Physiol; 2006; 47 (4):481-92 2006 Jan 31 PMID:16449231
Anti-inflammatory activity in vitro and in vivo of the protein farnesyltransferase inhibitor tipifarnib.
Xue X; Lai KT; Huang JF; Gu Y; Karlsson L; Fourie A;
J Pharmacol Exp Ther; 2005; 317 (1):53-60 2005 Dec 13 PMID:16352705