QIAGEN Plasmid Kits for Plasmid DNA Extraction.

For purification of up to 10 mg transfection-grade plasmid or cosmid DNA

S_2406_Qtips

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QIAGEN Plasmid Mini Kit (25)

Cat no. / ID.   12123

25 QIAGEN-tip 20, Reagents, Buffers
€181.00
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KitBufferColumnCartridge
Plasmid Kit
Plasmid Buffer Set
QIAGEN-tip
QIAfilter Cartridge
Column type
Mini
Midi
Maxi
Mega
Giga
Preparations
25
100
This product contains substances regulated under REACH (EC 1907/2006 Annex XIV). The use of this product in the EU is permitted subject to an exemption (Article 56(3)). Please refer to the REACH notification and the SDS of this product, both of which can be found in the “Resources” section of this page, for more information.
The QIAGEN Plasmid Mini Kit (25) is intended for molecular biology applications. This product is not intended for the diagnosis, prevention, or treatment of a disease.
QIAGEN 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

  • Purity equivalent to 2 x CsCl gradient centrifugation
  • High yields of plasmid DNA
  • Cost-effective preparations
  • LyseBlue for optimum lysis and maximum DNA yield

Product Details

QIAGEN Plasmid Kits provide gravity-flow, anion-exchange tips for purification of transfection-grade plasmid DNA. Lysate clearing and isopropanol precipitation are achieved by centrifugation.

The QIAGEN Plasmid Mega Kit (cat. no. 12181) and the QIAGEN Plasmid Giga Kit (cat. no. 12191) can be used with the QIAfilter Mega-Giga Cartridges (cat. no. 19781) as an optional protocol step for rapid clearing of bacterial lysates by filtration instead of centrifugation. See more information regarding principle below.

Performance

The QIAGEN Plasmid Kits uses gravity-flow QIAGEN anion-exchange tips for efficient purification of plasmid DNA. Up to 10 mg (giga), 2.5 mg (mega), 500 µg (maxi), 100 µg (midi), and 20 µg (mini) high-copy plasmid DNA is purified from culture (culture volumes depend on plasmid copy number, size of insert, host strain, and culture medium). Plasmid DNA purified with QIAGEN Plasmid Kits is highly suitable for use in applications such as transfection (see figure " Transfection efficiency versus plasmid purification method"), cloning, and in vitro transcription..

See figures

Principle

The unique anion-exchange resin in QIAGEN-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. Prepacked QIAGEN-tips operate by gravity flow and never run dry, minimizing the hands-on time required for plasmid preparation. The entire QIAGEN plasmid purification system avoids the use of toxic substances such as phenol, chloroform, ethidium bromide, and CsCl, minimizing hazard both to the user and the environment.

As an optional protocol step for rapid clearing of bacterial lysates by filtration instead of centrifugation, you can use the QIAfilter Mega-Giga Cartridges (cat. no. 19781), which operate with house vacuum to efficiently clear even large volumes of bacterial lysate with minimal effort. The protocol is available in the handbook.

Specifications

Features
Plasmid
Mini Kit
Plasmid
Midi Kit
Plasmid
Maxi Kit
Plasmid
Mega Kit
Plasmid
Giga Kit
Applications Transfection, cloning, sequencing, capillary sequencing, etc. Transfection, cloning, sequencing, capillary sequencing, etc. Transfection, cloning, sequencing, capillary sequencing, etc. Transfection, cloning, sequencing, capillary sequencing, etc. Transfection, cloning, sequencing, capillary sequencing, etc.
Culture volume/starting material 3–10 ml culture volume 25–100 ml culture volume 100–500 ml culture volume 500 ml – 2.5 liters culture volume 2.5–5 liters culture volume
Elution volume Variable Variable Variable Variable Variable
Plasmid type High-copy, low-copy, cosmid DNA High-copy, low-copy, cosmid DNA High-copy, low-copy, cosmid DNA High-copy, low-copy, cosmid DNA High-copy, low-copy, cosmid DNA
Processing Manual (gravity flow) Manual (gravity flow) Manual (gravity flow) Manual (gravity flow) Manual (gravity flow)
Sample per run 1 sample per run 1 sample per run 1 sample per run 1 sample per run 1 sample per run
Technology Anion-exchange technology Anion-exchange technology Anion-exchange technology Anion-exchange technology Anion-exchange technology
Time per run 80 min 150 min 160 min 220 min 320 min
Yield <20 µg up to 100 µg <500 µg <2.5 mg <10 mg

Procedure

With QIAGEN Plasmid Kits, bacterial lysates are cleared by centrifugation. The cleared lysate is then loaded onto the anion-exchange tip where plasmid DNA selectively binds under appropriate low-salt and pH conditions. RNA, proteins, metabolites, and other low-molecular-weight impurities are removed by a medium-salt wash, and pure plasmid DNA is eluted in high-salt buffer (see flowchart " QIAGEN Plasmid Kit procedures"). The DNA is concentrated and desalted by isopropanol precipitation and collected by centrifugation.

See figures

Applications

Plasmid DNA purified with QIAGEN Plasmid Kits is highly suitable for use in applications, such as:

  • Transfection
  • Cloning
  • PCR
  • In vitro transcription

Example 1 
  12123 12125 12143 12145 12145X4 12162 12163 12165
Product Plasmit Kit Plasmit Kit Plasmit Kit Plasmit Kit Plasmit Kit Plasmit Kit Plasmit Kit Plasmit Kit
Product Type Kit Kit Kit Kit Kit Kit Kit Kit
Column Type  Mini Mini MIDI MIDI MIDI MAXI MAXI MAXI
Preparations 25 100 25 100 400 10 25 100
Example 2
CatNo Product Product Type Column Type Preparations
12123 Plasmit Kit Kit Mini 25
12125 Plasmit Kit Kit Mini 100
12143 Plasmit Kit Kit MIDI 25
12145 Plasmit Kit Kit MIDI 100
12145X4 Plasmit Kit Kit MIDI 400
12162 Plasmit Kit Kit MAXI 10
12163 Plasmit Kit Kit MAXI 25
12165 Plasmit Kit Kit MAXI 100

Supporting data and figures

Specifications

FeaturesSpecifications
technologyAnion-exchange technology
culturevolumestartingmaterial3 ml–5 liters culture volume
yield<20 µg to <10 mg
processingManual (gravity flow)
samplesperrunthroughput1 sample per run
timeperrunorprepperrun80–320 min
applicationsTransfection, cloning, sequencing, capillary sequencing etc.
plasmidtypeHigh-copy, low-copy, cosmid DNA

Resources

Supplementary Protocols (8)
This protocol is designed for the rapid, easy, and non-toxic preparation of up to 2 mg genomic DNA from not more than 2 g of tissue using QIAGEN-tip 2500. QIAGEN® Genomic-tips 20/G, 100/G, and 500/G can also be used with this protocol by reducing the amount of starting material according to the table on page 2. The purified genomic DNA ranges in size from 50-150 kb.
This protocol is designed for isolation of up to 200 μg RNA from 150 mg plant tissue or up to 1 mg RNA from 600 mg plant tissue and is for use with QIAGEN-tip 100 or QIAGEN-tip 500, respectively.
This protocol is for purification of up to 100 µg endotoxin-free plasmid DNA using QIAGEN-tip 100.
This protocol is designed to provide up to 150 μg BAC/PAC/P1 DNA or up to 400 μg cosmid DNA.
Endotoxin-free DNA is essential for gene therapy research and will improve transfection into sensitive eukaryotic cells.
User-Developed Protocols (12)
The procedure has been used successfully for isolation of different medium-copy-number plasmids carrying pHM1519 or pBL1 origins of replication from Corynebacterium glutamicum ATCC 13032. Yield of plasmid DNA was typically 0.4-1.5 µg per ml LB culture, although yield was dependent on the vector, the insert, and the size of the plasmid.
The procedure has been used successfully for isolation of high- and low-copy-number plasmids from various Bacillus subtilis strains. Yield of plasmid DNA was typically 10-20 µg plasmid DNA from 100 ml culture.
The procedure has been used successfully for isolation of 110 kb P1 DNA (pAdsacBII with an 80 kb insert) from Escherichia coli strain NS3529. Yield of P1 DNA was typically 10-50 µg from 500 ml culture.
The procedure has been used successfully for isolation of a variety of medium-copy-number shuttle vectors from S. xylosus, S. carnosus, S. epidermidis, and S. aureus. Yield of plasmid DNA was typically 2-10 µg from 50 ml culture.
The procedure has been used successfully for isolation of cryptic plasmids (pLC2-based) from mesophilic Lactobacillus strains such as L. sake and L. curvatus. Yield of plasmid DNA was typically 10-20 µg plasmid DNA from 100 ml culture.
This procedure has been used successfully for isolation of 150-250 kb BAC DNA from a mouse-BAC library cloned in pBeloBAC11 from Escherichia coli strain HB101/r. The yield of BAC DNA from 100 ml culture was typically 20-40 μg.
The procedure has been used successfully for isolation of high-copy-number plasmids from Proteus vulgaris and Proteus mirabilis. Yield of plasmid DNA was typically 3-8 µg DNA per ml culture.
The procedure has been used successfully for isolation of plasmids SCP2 and SCP2* as well as the plasmids listed in Table 1 (see next page) from S. coelciolor and S. lividans strains.
The procedure has been used successfully for isolation of the large (128 kb), very-low-copynumber (1-2 copies per cell) plasmid pHCG3 and its derivatives from Oligotropha carboxidovorans. Yield of plasmid DNA was typically 3-6 µg plasmid DNA from 200 ml culture.
The procedure has been used successfully for isolation of linear plasmids from Borrelia burgdorferi sensu lato species, which include Borrelia burgdorferi sensu stricto, Borrelia afzelli, and Borrelia garinii.
The procedure has been used successfully for isolation of high-copy-number plasmids from Citrobacter freundii. Yield of plasmid DNA was typically 3-8 µg DNA per ml culture.
Safety Data Sheets (3)
Download Safety Data Sheets for QIAGEN product components.
Download Safety Data Sheets for QIAGEN product components.
Certificates of Analysis (1)

Publications

Oncocytic change in pleomorphic adenoma: molecular evidence in support of an origin in neoplastic cells.
Di Palma S; Lambros MB; Savage K; Jones C; Mackay A; Dexter T; Iravani M; Fenwick K; Ashworth A; Reis-Filho JS;
J Clin Pathol; 2006; 60 (5):492-9 2006 Feb 7 PMID:16467165
Haploinsufficiency of C2GnT-I glycosyltransferase renders T lymphoma cells resistant to cell death.
Cabrera PV; Amano M; Mitoma J; Chan J; Said J; Fukuda M; Baum LG;
Blood; 2006; 108 (7):2399-406 2006 Jun 15 PMID:16778138
RepAM of the Amycolatopsis methanolica integrative element pMEA300 belongs to a novel class of replication initiator proteins.
Te Poele EM; Kloosterman H; Hessels GI; Bolhuis H; Dijkhuizen L;
Microbiology (Reading); 2006; 152 (Pt 10):2943-2950 2006 Oct PMID:17005975
Involvement of Bcl-X(L) deamidation in E1A-mediated cisplatin sensitization of ovarian cancer cells.
Chang CY; Lin YM; Lee WP; Hsu HH; Chen EI;
Oncogene; 2006; 25 (18):2656-65 2006 Apr 27 PMID:16331250