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HiSpeed Plasmid Kits

For ultrafast purification of up to 750 µg transfection-grade plasmid or cosmid DNA

S_1376_DNA_PLS0763

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HiSpeed Plasmid Midi Kit (25)

Cat no. / ID.   12643

25 HiSpeed Midi Tips, 25 QIAfilter Midi Cartridges, 25 QIAprecipitator Midi Modules plus Syringes, Reagents, Buffers.
Cartridge type
Midi
Maxi
HiSpeed Plasmid 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

  • Less than 60 minutes prep time
  • Lysate clearing and isopropanol precipitation without centrifugation
  • No risk of DNA pellet loss during precipitation
  • Up to 750 µg yield of high-copy plasmid DNA
  • LyseBlue for optimum lysis and maximum DNA yield
  • Large-scale plasmid preparation without vacuum manifold

Product Details

HiSpeed Plasmid Kits provide fast, large-scale, anion-exchange-based plasmid DNA preparation without centrifugation. The purified DNA is equivalent to that obtained by 2 x CsCl gradient centrifugation and is suitable for transfection-grade applications.

Performance

HiSpeed Plasmid Kits contain QIAfilter Cartridges, HiSpeed Tips, and QIAprecipitator modules for fast large-scale plasmid preparation without vacuum manifold. Syringe-format QIAfilter and QIAprecipitator modules replace centrifugation steps in the classic anion-exchange procedure, making plasmid purification faster and more convenient. Up to 750 µg (maxi) or 200 µg (midi) high-copy plasmid DNA can be purified from 150 ml – 250 ml or 50 ml – 150 ml culture, respectively (culture volumes depend on plasmid copy number, size of insert, host strain, and culture medium). HiSpeed Tip design allows a very high flow rate, permitting DNA binding, washing, and elution steps for plasmid purification to proceed faster.

The unique anion-exchange resin in HiSpeed Tips is developed exclusively for the purification of nucleic acids. Its exceptional separation properties result in DNA purity equivalent or superior to that obtained by two successive rounds of CsCl gradient centrifugation.

Principle

QIAfilter Cartridges (see figure " QIAfilter Cartridge") are special filter units designed to replace the centrifugation step following alkaline lysis of bacterial cells. QIAfilter Cartridges completely remove SDS precipitates and clear bacterial lysates in a fraction of the time needed for centrifugation. Prepacked HiSpeed Tips operate by gravity flow and never run dry, minimizing the hands-on time required for plasmid preparation.

The unique QIAprecipitator module (see figure " QIAprecipitator module") replaces the centrifugation step traditionally used to collect isopropanol-precipitated DNA following purification. The QIAprecipitator module traps the precipitated DNA, while the isopropanol-buffer mixture flows through. The DNA is then simply eluted from the QIAprecipitator into a microcentrifuge tube with TE buffer or water. This unique module also eliminates the risk of pellet loss, which can occur during decanting of the supernatant following centrifugation.

Specifications
Features HiSpeed Plasmid Midi Kit HiSpeed Plasmid Maxi Kit
Applications Transfection, cloning sequencing, gene silencing Transfection, cloning sequencing, gene silencing
Culture volume/starting material 50 µl – 150 ml culture volume 150 µl – 250 ml culture volume
Plasmid type High-copy, cosmid DNA High-copy, cosmid DNA
Processing Manual (filtration) Manual (filtration)
Sample per run 1 sample per run 1 sample per run
Technology Anion-exchange technology Anion-exchange technology
Time per run 45 min 60 min
Yield <200 µg <750 µg

Procedure

Neutralized bacterial lysates are incubated in the QIAfilter Cartridge and cleared in seconds by filtration. The filtrate is applied to a HiSpeed tip for plasmid DNA purification (see flowchart " QIAGEN Plasmid Kit procedures"). Eluted DNA is mixed with isopropanol and applied to the QIAprecipitator module using the syringe provided. The concentrated and desalted DNA is then eluted from the QIAprecipitator directly into a microcentrifuge tube with TE buffer or water.

Applications

DNA purified with HiSpeed Plasmid Kits yield excellent results in all applications, from cloning and sequencing to transfection and plasmid-mediated gene silencing.

Supporting data and figures

Resources

Safety Data Sheets (1)
Download Safety Data Sheets for QIAGEN product components.
Certificates of Analysis (1)

Publications

Characterization of Helicobacter pylori lytic transglycosylases Slt and MltD.
Chaput C; Labigne A; Boneca IG;
J Bacteriol; 2006; 189 (2):422-9 2006 Nov 3 PMID:17085576
Identification of a lipase-linked cell membrane receptor for pigment epithelium-derived factor.
Notari L; Baladron V; Aroca-Aguilar JD; Balko N; Heredia R; Meyer C; Notario PM; Saravanamuthu S; Nueda ML; Sanchez-Sanchez F; Escribano J; Laborda J; Becerra SP;
J Biol Chem; 2006; 281 (49):38022-37 2006 Oct 10 PMID:17032652
Role of parathyroid hormone in the downregulation of liver cytochrome P450 in chronic renal failure.
Michaud J; Naud J; Chouinard J; Désy F; Leblond FA; Desbiens K; Bonnardeaux A; Pichette V;
J Am Soc Nephrol; 2006; 17 (11):3041-8 2006 Oct 4 PMID:17021269
A rapid functional assay for the human trace amine-associated receptor 1 based on the mobilization of internal calcium.
Navarro HA; Gilmour BP; Lewin AH;
J Biomol Screen; 2006; 11 (6):688-93 2006 Jul 10 PMID:16831861
Engineering of a xylose metabolic pathway in Corynebacterium glutamicum.
Kawaguchi H; Vertès AA; Okino S; Inui M; Yukawa H;
Appl Environ Microbiol; 2006; 72 (5):3418-28 2006 May PMID:16672486

FAQ

How can I improve the performance of the HiSpeed QIAprecipitator module?

When using the QIAprecipitator module of the HiSpeed Plasmid Midi- or Maxi Kits, make sure to dry the membrane by pressing air through the QIAprecipitator at least twice. Dry the outlet nozzle of the QIAprecipitator with absorbent paper. This will prevent carry-over of alcohol into the eluate and enable optimal performance of the extracted DNA downstream.

Do not load eluate from from several columns on the QIAprecipitator, and be sure that the correct precipitator size is used for the corresponding HiSpeed Tip. Do not replace the isopropanol with ethanol for precipitation, since the use of ethanol will lead to a finer precipitate that can clog the module.

To prevent breakage and leakage of the module it is important to avoid excessive force, bending, or twisting while attaching the QIAprecipitator to the syringe. Do not stress the inlet by resting one edge of the QIAprecipitator on a hard surface (e.g., the edge of a sink) and depressing the syringe plunger. Always apply gentle, even, pressure perpendicularly to the QIAprecipitator.

FAQ-144
What is the RNase A concentration and composition of Buffer P1?

The composition of Buffer P1 is:

  • 50 mM Tris·Cl, pH 8.0
  • 10 mM EDTA
  • 100 µg/ml RNase A

After RNase A addition, the buffer should be stored at 2–8°C.

Buffer P1 is the resuspension buffer used in a variety of QIAGEN kits for plasmid DNA purification. Details on buffer preparation and storage are presented in Appendix B of the QIAGEN Plasmid Purification Handbook.

FAQ-198