QIAprep 96 Turbo Miniprep Kit

For purification of up to 20 µg molecular biology grade plasmid DNA per well

S_1084_5_GEN_disclaimer

✓ 연중무휴 하루 24시간 자동 온라인 주문 처리

✓ 풍부한 지식과 전문성을 갖춘 제품 및 기술 지원

✓ 신속하고 안정적인 (재)주문

QIAprep 96 Turbo Miniprep Kit (4)

카탈로그 번호 / ID.   27191

For 4 x 96 high-purity plasmid minipreps, 4 each: TurboFilter 96 and QIAprep 96 Plates; S-Blocks, reagents, buffers, collection microtubes (1.2 ml), caps
€1,559.00
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KitPlate
QIAprep 96 Turbo Kit
QIAprep 96 Turbo Core Kit
TurboFilter 96 Plates
QIAprep 96 Plates
다음의 경우
QIAvac 96
BioRobot Universal
준비
4 x 96
24 x 96
QIAprep 96 Turbo Miniprep Kit은/는 분자생물학 분야에 사용하기 위한 것입니다. 이 제품들은 질병의 진단, 예방, 또는 치료 목적으로 사용할 수 없습니다.

✓ 연중무휴 하루 24시간 자동 온라인 주문 처리

✓ 풍부한 지식과 전문성을 갖춘 제품 및 기술 지원

✓ 신속하고 안정적인 (재)주문

특징

  • 효율적 분리 정제
  • 45분 안에 ready-to-use plasmid DNA로 분리 정제
  • Molecular biology grade plasmid DNA의 재현성 있는 yield

제품 세부 정보

The QIAprep 96 Turbo Miniprep Kit provides QIAprep 96 and TurboFilter 96 plates for purification of up to 20 µg molecular biology grade plasmid DNA per well.

성능

The QIAprep 96 Turbo Miniprep Kit is designed for isolation of up to 20 µg pure plasmid or cosmid DNA for use in routine molecular biology applications, such as sequencing and cloning (see figure "High-quality DNA for automated sequencing").

In addition to plasmid purification from Escherichia coli, QIAprep Kits can be used to purify plasmid DNA from Saccharomyces cerevisiae, Bacillus subtilis, and Agrobacterium tumefaciens. Contact QIAGEN Technical Services or your local distributor for protocols for these applications.

원리

QIAprep 96 plates contain a unique silica membrane that binds up to 20 µg DNA in the presence of a high concentration of chaotropic salt, and allows elution in a small volume of low-salt buffer. QIAprep membrane technology eliminates time consuming phenol–chloroform extraction and alcohol precipitation, as well as the problems and inconvenience associated with loose resins and slurries. Pure plasmid DNA eluted from QIAprep 96 plates is immediately ready to use — there is no need to precipitate, concentrate, or desalt.

TurboFilter 96 plates are specially designed to allow fast clearing of bacterial lysates generated under high concentrations of chaotropic salts. Crude bacterial lysates are vacuum filtered through the TurboFilter 96 plate, eliminating the need for centrifugation. Particle-free lysates flow directly into the wells of the QIAprep 96 plate, ready for purification and elution. TurboFilter technology streamlines QIAprep plasmid purification.

절차

Plasmid purification using QIAprep 96 Turbo Miniprep Kits follows a simple bind–wash–elute procedure (see flowchart "The QIAprep procedure"). First, bacterial cultures are lysed and the lysates are cleared by filtration through TurboFilter modules. The cleared lysates are then applied to the QIAprep 96 plate where plasmid DNA adsorbs to the silica membrane. Impurities are washed away and pure DNA is eluted in a small volume of elution buffer or water.

The QIAprep 96 Turbo procedure is performed entirely in 96-well format, reducing sample handling to a minimum, allowing 96 parallel minipreps to be processed in 45 minutes. Bacterial cultures can be grown and lysed in the 96-well blocks provided with the kit. The QIAvac 96 manifold is designed for in-line filtration in 96-well format, so that cleared lysates from the TurboFilter 96 plate flow directly into the wells of the QIAprep 96 plate, providing high-throughput of 96 samples in parallel.  

응용 분야

QIAprep 96 Turbo Miniprep Kits provide reproducible yields of pure DNA suitable for use in many applications, including:

  • Screening
  • PCR 
  • Sequencing
  • Restriction digestion
  • Ligation and transformation

리소스

Kit Handbooks (1)
Supplementary Protocols (2)
This protocol is designed for 96 parallel plasmid DNA preparations from 1.3 ml overnight cultures.
Safety Data Sheets (1)
Download Safety Data Sheets for QIAGEN product components.
Certificates of Analysis (1)

출판물

Systematic variation in mRNA 3'-processing signals during mouse spermatogenesis.
Liu D; Brockman JM; Dass B; Hutchins LN; Singh P; McCarrey JR; MacDonald CC; Graber JH;
Nucleic Acids Res; 2006; 35 (1):234-46 2006 Dec 8 PMID:17158511
Constraints on HIV-1 evolution and immunodominance revealed in monozygotic adult twins infected with the same virus.
Draenert R; Allen TM; Liu Y; Wrin T; Chappey C; Verrill CL; Sirera G; Eldridge RL; Lahaie MP; Ruiz L; Clotet B; Petropoulos CJ; Walker BD; Martinez-Picado J;
J Exp Med; 2006; 203 (3):529-39 2006 Mar 13 PMID:16533886
Regulation of gene expression in magnocellular neurons in rat supraoptic nucleus during sustained hypoosmolality.
Mutsuga N; Shahar T; Verbalis JG; Xiang CC; Brownstein MJ; Gainer H;
Endocrinology; 2004; 146 (3):1254-67 2004 Dec 9 PMID:15591143
Genome-scale cloning and expression of individual open reading frames using topoisomerase I-mediated ligation.
Heyman JA; Cornthwaite J; Foncerrada L; Gilmore JR; Gontang E; Hartman KJ; Hernandez CL; Hood R; Hull HM; Lee WY; Marcil R; Marsh EJ; Mudd KM; Patino MJ; Purcell TJ; Rowland JJ; Sindici ML; Hoeffler JP;
Genome Res; 1999; 9 (4):383-92 1999 Apr PMID:10207160
Positional cloning of the gene for X-linked retinitis pigmentosa 2.
Schwahn U; Lenzner S; Dong J; Feil S; Hinzmann B; van Duijnhoven G; Kirschner R; Hemberger M; Bergen AA; Rosenberg T; Pinckers AJ; Fundele R; Rosenthal A; Cremers FP; Ropers HH; Berger W;
Nat Genet; 1998; 19 (4):327-32 1998 Aug PMID:9697692