플라스미드 DNA 추출을 위한 QIAGEN Plasmid Kits

Transfection grade의 plasmid 혹은 cosmid DNA을 10 mg까지 분리 정제할 수 있습니다

S_2406_Qtips

✓ 연중무휴 하루 24시간 자동 온라인 주문 처리

✓ 풍부한 지식과 전문성을 갖춘 제품 및 기술 지원

✓ 신속하고 안정적인 (재)주문

QIAGEN Plasmid Mini Kit (25)

카탈로그 번호 / ID.   12123

25 QIAGEN-tip 20, Reagents, Buffers
KitBufferColumnCartridge
Plasmid Kit
Plasmid Buffer Set
QIAGEN-tip
QIAfilter Cartridge
컬럼 유형
Mini
Midi
Maxi
Mega
Giga
준비
25
100
이 제품에는 REACH(EC 1907/2006 부속서 XIV)에 따라 규제되는 물질이 포함되어 있습니다. EU에서 이 제품의 사용은 예외 조항(56조 3항)에 따라 허용됩니다. 자세한 내용은 이 페이지의 ‘Resources’(리소스) 부분에서 확인할 수 있는 이 제품의 REACH 고지 및 SDS를 참조하시기 바랍니다.
QIAGEN Plasmid Mini Kit (25)은/는 분자생물학 분야에 사용하기 위한 것입니다. 이 제품은 질병의 진단, 예방, 또는 치료용이 아닙니다.
QIAGEN Plasmid Kits은/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

  • CsCl 농도구배 원심분리 두 번 한 것과 같은 동일한 순도
  • Transfection grade plasmid DNA 의 재현성 있는 yield.
  • Ethidium bromide, phenol, chloroform, 또는 CsCl 불필요
  • 경제적인 preparation이 가능함

제품 세부 정보

QIAGEN Plasmid Kits provide gravity-flow, anion-exchange tips for purification of transfection-grade plasmid DNA. The QIAGEN Plasmid Giga Kit delivers DNA yields of up to 10 mg. Lysate clearing and isopropanol precipitation are achieved by centrifugation.

성능

The QIAGEN Plasmid Giga Kit uses gravity-flow QIAGEN-tip 10000 anion-exchange tips for efficient purification of plasmid DNA. Up to 10 mg high-copy plasmid DNA is purified from 2.5–5 liters 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.

원리

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.

절차

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. 

응용 분야

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

지원되는 데이터 및 수치

사양

특징사양
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

리소스

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)

출판물

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