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当前位置: 首页 > 产品中心 > peptide > Qiagen/RNeasy Maxi Kit/12 RNeasy Maxi Spin Columns, Collection Tubes (50 ml), RNase-free Reagents and Buffers/75162
商品详细Qiagen/RNeasy Maxi Kit/12 RNeasy Maxi Spin Columns, Collection Tubes (50 ml), RNase-free Reagents and Buffers/75162
Qiagen/RNeasy Maxi Kit/12 RNeasy Maxi Spin Columns, Collection Tubes (50 ml), RNase-free Reagents and Buffers/75162
Qiagen/RNeasy Maxi Kit/12 RNeasy Maxi Spin Columns, Collection Tubes (50 ml), RNase-free Reagents and Buffers/75162
商品编号: 75162
品牌: Qiagen
市场价: ¥7480.00
美元价: 4488.00
产地: 美国(厂家直采)
公司:
产品分类: 多肽合成
公司分类: peptide
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍

RNeasy Maxi Kit

Product picture
For purification of up to 6 mg total RNA from cells, tissues, and yeast
  • Fast procedure delivering high-quality total RNA in minutes
  • Ready-to-use RNA for high performance in any downstream application
  • Consistent RNA yields from large amounts of starting material
  • No phenol/chloroform extraction
  • No CsCl gradients, no LiCl or ethanol precipitation

The RNeasy Maxi Kit provides fast purification of high-quality RNA from cells, tissues, and yeast using silica-membrane RNeasy spin columns with a binding capacity of 6 mg RNA. Tissue samples can be conveniently stabilized using RNAprotect TissueReagent or Allprotect Tissue Reagent, and efficiently disrupted using a TissueRuptor or TissueLyser system. For smaller samples, the RNeasy Micro Kit (spin-column binding capacity of up to 45 µg RNA), the RNeasy Mini Kit (spin-column binding capacity of 100 µg RNA), and RNeasy Midi Kit (spin-column binding capacity of 1 mg RNA) are also available.

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Cat No./ID:75162
RNeasy Maxi Kit (12)
$374.00
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12 RNeasy Maxi Spin Columns, Collection Tubes (50 ml), RNase-free Reagents and Buffers
The RNeasy Maxi Kit is intended for molecular biology applications. This product is not intended for the diagnosis, prevention, or treatment of a disease.

Product Details

9
RNeasy Maxi spin column.
The RNeasy Maxi spin column contained in the RNeasy Maxi Kit.
9
High-quality RNA from a variety of samples.
9
RNeasy Maxi procedure.

RNeasy Kits provide the highest-quality RNA with minimum copurification of DNA. An additional buffer (composition provided) is required for isolation of cytoplasmic RNA from eukaryotic cells. Lyticase, zymolase, or glass beads (required for yeast samples) are not provided. Amounts of RNA isolated from samples can vary due to the developmental stage, species, and growth conditions of the sample source. Since the RNeasy procedure enriches for RNA species >200 nt, RNA yield does not include 5S rRNA, tRNAs, or other low-molecular-weight RNAs.

Performance

Total RNA purified with the RNeasy Maxi Kit is of high quality and is suitable for many downstream applications (see figure "High-quality RNA from a variety of samples"). Total RNA is easily purified with the RNeasy Maxi Kit from large amounts of starting material including animal or human cells, animal or human tissues, and yeast cells (see table).

Total RNA yields obtained with the RNeasy Maxi Kit
Source Starting materialAverage yield (mg)
Animal cells
LMH 5 x 108 5.7
HeLa 4 x 108 6.0
COS-7 1.8 x 108 5.8
Lymphocytes (unstimulated) 5 x 108 0.3
Mouse tissue
Liver 1 g 3.6
Lung 0.5 g 0.6
Spleen 1 g 3.2
Yeast cells
S. cerevisiae 1 x 109 2.4
Principle

The RNeasy Maxi Kit delivers efficient purification of total RNA from large amounts of starting material. RNeasy technology simplifies total RNA isolation by combining the stringency of guanidine-isothiocyanate lysis with the speed and purity of silica-membrane purification. Total RNA is easily purified from animal or human cells, animal or human tissues, and yeast. Protocols are included in the kit for cleanup of partially purified RNA, in vitro transcripts, and RNA from enzymatic reactions. RNeasy purified nucleic acids can be used in any molecular assay or other downstream application.

Procedure
RNeasy technology simplifies total RNA isolation. Samples (up to 5 x 108 animal or human cells, 2.5 x 109 yeast cells, or 150 mg to 1 g tissue) are first lysed and then homogenized. Ethanol is added to the lysate to provide ideal binding conditions. The lysate is then loaded onto the RNeasy silica membrane (see figure "RNeasy Maxi spin column"). RNA (up to 6 mg) binds to the membrane, and all contaminants are efficiently washed away. Residual amounts of DNA can be removed using the convenient on-column DNase treatment. Pure, concentrated RNA is eluted in 800–2400 µl water (see figure "RNeasy Maxi procedure"). A variety of special application protocols is also available.
Applications

RNA purified with RNeasy technology has A260/280 ratios of 1.9–2.1 (measured in 10 mM Tris·Cl, pH 7.5)and is ideal for use in all applications. Downstream applications include:

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

Specifications

Features
Specifications
ApplicationsPCR, qPCR, real-time RT-PCR, microarray
Elution volume800–2400 µl
FormatSpin column
Main sample typeTissue, cells
ProcessingManual
Purification of total RNA, miRNA, poly A+ mRNA, DNA or proteinRNA
Sample amount150 mg – 1 g
TechnologySilica technology
Time per run or per prep1 hour
YieldVaries

Product Resources

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Brochures & Guides (3)
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All insights start with the sample: Your comprehensive guide for isolating top-quality RNA
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(EN) - Analyzing Gene Expression and Regulation
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Product Profile - RNeasy® Mini, Midi and Maxi Kits
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FAQs (43)
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How do I safely inactivate biohazardous flow-through material?
FAQ ID -12
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How should I quantify RNA isolated with RNeasy Kits?
FAQ ID -32
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Why does my isolated RNA have a low OD 260/280 ratio?
FAQ ID -97
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How can I avoid little or no RNA yields when using an RNeasy Kit?
FAQ ID -28
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Why do I have to add beta-mercaptoethanol (beta-ME) to lysis Buffer RLT of the RNeasy Kits?
FAQ ID -101
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How should RNeasy Kits be stored and how long are they stable?
FAQ ID -103
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How do you ensure that RNeasy buffers are RNase-free?
FAQ ID -113
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How can I isolate RNA from 1 gram of plant tissue?
FAQ ID -128
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What is the difference between disruption and homogenization in the RNeasy System?
FAQ ID -139
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How can I obtain DNA-free RNA using an RNeasy Midi or Maxi Kit?
FAQ ID -143
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Are RNeasy spin columns sold separately?
FAQ ID -159
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How can I check for purity of RNA isolated using RNeasy Kits?
FAQ ID -1023
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How can I check the integrity of RNA purified using RNeasy Kits?
FAQ ID -1024
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Which kit should I use for RNA isolation from Cartilage?
FAQ ID -1026
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Do I have to discard Buffer RLT with beta-Mercaptoethanol (ß-ME) added to it after 1 month of storage?
FAQ ID -1037
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What is the difference between Buffers RLT and RLT Plus?
FAQ ID -1043
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How can I ensure complete genomic DNA removal when using the RNase-Free DNase Set?
FAQ ID -1087
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What is the maximum volume of RNA in solution that can be used with the QuantiTect Whole Transcriptome Kit?
FAQ ID -1616
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Have you observed co-amplification of genomic DNA from RNA templates used in the QuantiTect Whole Transcriptome Procedure?
FAQ ID -1619
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Can I clean up my DNase treated RNA samples using RNeasy columns?
FAQ ID -286
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What is the maximum binding capacity of RNeasy spin columns?
FAQ ID -290
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Effects of low A260/A230 ratios in RNA preparations on downstream applications
FAQ ID -2248
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What is the composition of Buffer RLT?
FAQ ID -2793
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What is the composition of Buffer RW1?
FAQ ID -2796
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What is the composition of Buffer RPE?
FAQ ID -2797
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What is the composition of Buffer RDD?
FAQ ID -2800
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Can I buy the RNeasy Mini columns, RNeasy MinElute columns, RNeasy Midi columns or the RNeasy Maxi columns separately?
FAQ ID - 3388
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What has to be done to an RNA sample before loading it onto an Agilent Bioanalyzer?
FAQ ID -528
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Is it possible to isolate both RNA and recombinant 6xHis-tagged protein from the same sample?
FAQ ID -532
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Do you have a protocol for isolating RNA from yeast using RNeasy?
FAQ ID -535
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Do you offer QIAshredder spin columns for the RNeasy Midi/Maxi Kit format? If not, what is the alternative?
FAQ ID -560
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What do you recommend for isolating RNA from more than 100 mg of plant tissue?
FAQ ID -570
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Can the QIAshredder Maxi Spin Columns from the DNeasy Plant Maxi Kit be used for RNeasy samples?
FAQ ID -616
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Can the RNase-Free DNase Set be used for DNase digestions of RNA in solution?
FAQ ID -619
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How can I improve my RNA yield from liver sample when using RNeasy Kits?
FAQ ID -623
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How can I minimize degradation of RNA from my pancreas sample?
FAQ ID -624
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Do you have a kit for RNA isolation from any kind of sample type?
FAQ ID -627
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What is a QIAshredder? Is it sufficient for complete disruption and homogenization of my tissue sample?
FAQ ID -631
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What can be used as an alternative to the A260 measurement for quantification of small amounts of RNA and DNA?
FAQ ID -728
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I accidentally stored Buffer RDD of the RNase-Free DNase Set at°C. Will it still function?
-20
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I ran my RNA out on an agarose gel and can see lots of bands similar to a ladder. Why?
FAQ ID -745
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Do I need to use RNase inhibitors with the RNeasy Kits?
FAQ ID -813
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What do you suggest to prevent degradation of RNA isolated from tissue with high amounts of RNases using RNeasy?
FAQ ID -942
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Kit Handbooks (1)
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RNeasy Midi/Maxi Handbook

For total RNA isolation from animal cells, animal tissues, bacteria, yeast, whole blood, and for RNA cleanup

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Supplementary Protocols (3)
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Acetone precipitation of protein from Buffer RLT or Buffer RLT Plus lysates - (EN)
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RNeasy Midi/Maxi Protocol for Isolation of Cytoplasmic RNA from Animal Cells
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RNeasy® Midi/Maxi Protocol for Isolation of Total RNA from Bacteria
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Quick-Start Protocols (1)
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RNeasy Maxi Kit (EN)
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User-Developed Protocols (1)
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Purification of total RNA, including small RNAs, using the RNeasy® Maxi Kit - (EN)
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Safety Data Sheets (2)
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MSDS RNeasy Maxi Kit (12)
CofA
References
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品牌介绍
QIAGEN是一家专业化致力于生物分子样品制备解决方案的跨国经营企业,总部位于德国。1984年,QIAGEN在德国成立,1996年在美国纽约纳斯达克上市。QIAGEN拥有超过1000项专利和认可证明,在18个国家设立了分公司,代理商服务国超过40个,在全球有超过400000的用户。QIAGEN提供的产品超过500类,包括各种试剂,耗材和自动化纯化工作站。这些产品用于样品采集,稳定,核酸或蛋白的分离,纯化和检测中,不仅广泛的应用于科研领域的各个方面,在生物技术,制药,法医研究,食品安全检测,畜牧业和分子诊断领域也得到了广泛的应用。QIAGEN产品的卓越品质和在应用中的出色表现使得其成为样品处理中标准的代名词。