RNeasy MinElute Cleanup Kit – RNA Cleanup and Concentration

RNA를 clean-up을 할 수 있고 적은 elution volume으로 농축할 수 있습니다

S_1265_GEF_RNALT0157

✓ 연중무휴 하루 24시간 자동 온라인 주문 처리

✓ 풍부한 지식과 전문성을 갖춘 제품 및 기술 지원

✓ 신속하고 안정적인 (재)주문

RNeasy MinElute Cleanup Kit (50)

카탈로그 번호 / ID.   74204

50 RNeasy MinElute Spin Columns, Collection Tubes (1.5 ml and 2 ml), RNase-free Reagents and Buffers
MX$11,794.00
로그인 계정 가격 보기.
RNeasy MinElute Cleanup 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

  • RNase, nucleotide 제거 외에 labeling 같은 효소 반응으로 부터의 효율적인 정제
  • 민감도 높은 실험을 위해 10ul로 RNA를 농축할 수 있음
  • 다른 방법으로 추출된 RNA 정제 — e.g., crude preps from organic extraction methods
  • 15분안에 양질의 RNA 추출 — 침전 과정, vacuum 과정, 원심 분리 과정 없음

제품 세부 정보

The RNeasy MinElute Cleanup Kit enables cleanup and concentration of RNA from enzymatic reactions or other samples using specialized RNeasy MinElute spin columns based on silica-membrane technology. The kit can also be used to desalt RNA samples. Up to 45 μg RNA can be purified in a volume as low as 10 μl. Purification can be fully automated on the QIAcube.

성능

The RNeasy MinElute Cleanup Kit provides high-quality total RNA, free from impurities or enzymatic inhibitors, with A260/A280 ratios of 1.9–2.1 (see figure " High-quality RNA"). RNA amounts corresponding to less than one cell (as little as 1 pg) can be concentrated (see figure " Concentration of RNA"). A large amount of RNA (up to 45 µg) can be purified and is suitable for use in sensitive assays (see figure "Reliable cleanup of RNA").  Reaction volumes can be kept small in downstream applications, giving increased reaction efficiency. The high purity RNA allows more of the sample to be used in reactions without inhibition (see figure " Efficient removal of real-time RT-PCR inhibitors").
그림 참조

원리

The RNeasy MinElute Cleanup Kit is designed to purify and concentrate RNA from enzymatic reactions (e.g., labeling, in vitro transcription), RNA isolated by alcohol-precipitation and organic-extraction methods, as well as to desalt RNA samples, and concentrate RNA prepared by silica-membrane procedures (e.g., PAXgene Blood RNA preps). RNeasy technology simplifies total RNA isolation by combining guanidine-isothiocyanate lysis with silica-membrane purification.

절차

Guanidine-isothiocyanate–containing lysis buffer and ethanol are added to the sample to create conditions that promote selective binding of RNA to the RNeasy MinElute membrane. The sample is then applied to the RNeasy MinElute spin column. RNA binds to the silica-membrane, contaminants are efficiently washed away, and high-quality RNA is eluted in water.

Enzymatic reactions or crude RNA preps are simultaneously cleaned up and concentrated in less than 15 minutes. In comparison, time-consuming concentration and cleanup by alcohol precipitation can result in loss of RNA, especially from small samples. The RNeasy MinElute procedure is faster than vacuum centrifugation, which only concentrates the sample without removing salts and other impurities. The unique design of RNeasy MinElute spin columns enables concentration of purified RNA to as little as 10 µl for downstream applications such as microarray analysis and real-time RT-PCR. Purification can be fully automated on the QIAcube.

응용 분야

RNA purified with RNeasy MinElute technology is high-quality and ideal for use in all applications including:

  • Northern, dot, and slot blotting
  • End-point RT-PCR
  • Quantitative, real-time RT-PCR
  • Array analysis
  • Poly A+ RNA selection

지원되는 데이터 및 수치

사양

특징사양
applicationsPCR, qPCR, real-time PCR, microarray
formatMinElute Spin column
sampleamount200 µl
elutionvolume10–14 µl
processingManual
mainsampletype(Crude) RNA preps
purificationoftotalrnamirnapolyamrnadnaorproteinRNA
timeperrunorperprep<15 minutes
technologySilica technology
yield45 µg

리소스

Kit Handbooks (1)
Safety Data Sheets (1)
Download Safety Data Sheets for QIAGEN product components.
Supplementary Protocols (2)
There are two protocols: follow Protocol 1 if you want to purify total RNA containing miRNA, or follow Protocol 2 if you want to purify small RNA (includes miRNA, 5S rRNA, and tRNA) and larger RNA (>200 nt) separately.
Quick-Start Protocols (1)
Gene Expression Analysis (1)
Certificates of Analysis (1)

출판물

Silencing of stathmin induces tumor-suppressor function in breast cancer cell lines harboring mutant p53.
Alli E; Yang JM; Hait WN;
Oncogene; 2006; 26 (7):1003-12 2006 Aug 14 PMID:16909102
The extracellular nucleotide UTP is a potent inducer of hematopoietic stem cell migration.
Rossi L; Manfredini R; Bertolini F; Ferrari D; Fogli M; Zini R; Salati S; Salvestrini V; Gulinelli S; Adinolfi E; Ferrari S; Di Virgilio F; Baccarani M; Lemoli RM;
Blood; 2006; 109 (2):533-42 2006 Sep 28 PMID:17008551
The lspA gene, encoding the type II signal peptidase of Rickettsia typhi: transcriptional and functional analysis.
Rahman MS; Ceraul SM; Dreher-Lesnick SM; Beier MS; Azad AF;
J Bacteriol; 2006; 189 (2):336-41 2006 Nov 10 PMID:17098907
Selection and cloning of poly(rC)-binding protein 2 and Raf kinase inhibitor protein RNA activators of 2',5'-oligoadenylate synthetase from prostate cancer cells.
Molinaro RJ; Jha BK; Malathi K; Varambally S; Chinnaiyan AM; Silverman RH;
Nucleic Acids Res; 2006; 34 (22):6684-95 2006 Dec 1 PMID:17145707
Additional freeze hardiness in wheat acquired by exposure to -3 degreesC is associated with extensive physiological, morphological, and molecular changes.
Herman EM; Rotter K; Premakumar R; Elwinger G; Bae H; Ehler-King L; Chen S; Livingston DP 3rd;
J Exp Bot; 2006; 57 (14):3601-18 2006 Sep 12 PMID:16968883