QIAGEN Large-Construct Kit

150 ug BAC, PAC, and P1 DNA를 150 ug까지 혹은 cosmid DNA, free of genomic DNA 400 ug까지 분리 정제할 수 있습니다

S_2712_ADNA_Qlargeconstruct_s

✓ 연중무휴 하루 24시간 자동 온라인 주문 처리

✓ 풍부한 지식과 전문성을 갖춘 제품 및 기술 지원

✓ 신속하고 안정적인 (재)주문

QIAGEN Large-Construct Kit (10)

카탈로그 번호 / ID.   12462

10 QIAGEN-tip 500, Reagents, Buffers, ATP-Dependent Exonuclease
MX$13,963.00
로그인 계정 가격 보기.
QIAGEN Large-Construct Kit은/는 분자생물학 분야에 사용하기 위한 것입니다. 이 제품은 질병의 진단, 예방, 또는 치료용이 아닙니다.

✓ 연중무휴 하루 24시간 자동 온라인 주문 처리

✓ 풍부한 지식과 전문성을 갖춘 제품 및 기술 지원

✓ 신속하고 안정적인 (재)주문

특징

  • 효율적인 genomica DNA contamination 제거
  • Transfection grade의 large-construct DNA
  • 빠르고 간단한 처리과정

제품 세부 정보

The QIAGEN Large-Construct Kit provides gravity-flow, anion-exchange columns for purification of large-molecular-weight DNA. A unique integrated ATP-dependent exonuclease digestion step ensures selective removal of contaminating genomic DNA. The purified DNA is equivalent to that obtained by 2 x CsCl gradient centrifugation and is suitable for transfection.

성능

DNA purified using the QIAGEN Large-Construct Kit is free of genomic DNA contamination (see figure "Efficient removal of genomic DNA"). This removal of genomic DNA ensures accurate and reliable DNA quantitation, which enables sensitive experiments to be carried out under defined and reproducible conditions.

원리

DNA purification using the QIAGEN Large-Construct  Kit uses an optimized gravity-flow procedure which yields DNA of significantly greater purity than that obtained with other commonly used methods. A unique integrated treatment with ATP-Dependent Exonuclease enables efficient removal of genomic DNA.

The unique anion-exchange resin in QIAGEN-tips, included in the QIAGEN Large-Construct Kit, 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 (see figure " Anion-exchange 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.

그림 참조

절차

Following alkaline lysis of up to 500 ml culture (see flowchart " QIAGEN Plasmid Kit procedures"), a unique integrated digestion step with ATP-dependent exonuclease provided with the kit, ensures selective removal of contaminating genomic DNA, as well as nicked or damaged construct DNA. The sample 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. Genomic DNA-free, pure plasmid DNA is eluted in high-salt buffer. The DNA is concentrated and desalted by isopropanol precipitation and collected by centrifugation.

그림 참조

응용 분야

DNA purified using the QIAGEN Large-Construct Kit is suitable for any application, including:

  • Subcloning and preparation of shotgun libraries
  • Direct sequencing of large-construct DNA
  • Transfection

지원되는 데이터 및 수치

사양

특징사양
plasmidtypeBAC, PAC, P1, cosmid DNA
applicationsSubcloning, transfection, sequencing etc.
processingManual (centrifugation)
culturevolumestartingmaterial<500 ml culture volume
samplesperrunthroughput1 sample per run
technologyAnion-exchange technology
timeperrunorprepperrun280 min
yield<150 ug

리소스

Quick-Start Protocols (2)
Safety Data Sheets (1)
Download Safety Data Sheets for QIAGEN product components.
Certificates of Analysis (1)

출판물

Functional characterization of Kaposi's sarcoma-associated herpesvirus ORF45 by bacterial artificial chromosome-based mutagenesis.
Zhu FX; Li X; Zhou F; Gao SJ; Yuan Y;
J Virol; 2006; 80 (24):12187-96 2006 Oct 11 PMID:17035322
Autographa californica multiple nucleopolyhedrovirus nucleocapsid assembly is interrupted upon deletion of the 38K gene.
Wu W; Lin T; Pan L; Yu M; Li Z; Pang Y; Yang K;
J Virol; 2006; 80 (23):11475-85 2006 Sep 20 PMID:16987976
Identification of in vivo-induced bacterial protein antigens during human infection with Salmonella enterica serovar Typhi.
Harris JB; Baresch-Bernal A; Rollins SM; Alam A; LaRocque RC; Bikowski M; Peppercorn AF; Handfield M; Hillman JD; Qadri F; Calderwood SB; Hohmann E; Breiman RF; Brooks WA; Ryan ET;
Infect Immun; 2006; 74 (9):5161-8 2006 Sep PMID:16926408
Molecular characterization of a diagnostic DNA marker for domesticated tetraploid wheat provides evidence for gene flow from wild tetraploid wheat to hexaploid wheat.
Dvorak J; Akhunov ED; Akhunov AR; Deal KR; Luo MC;
Mol Biol Evol; 2006; 23 (7):1386-96 2006 May 4 PMID:16675504