QIAamp DSP Virus Kit

从人类血清或血浆中纯化病毒核酸

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QIAamp DSP Virus Kit

Cat. No. / ID:   60704

For 50 preps: QIAamp MinElute Columns, buffers, reagents, tubes, column extenders, VacConnectors
€510.00
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QIAamp DSP Virus Kit适用于体外诊断。

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特点

  • 通用的核酸纯化系统
  • 获得高品质病毒核酸
  • 浓缩的核酸,洗脱体积为20 μl或60 μl
  • 上样量为500 µl
  • 快速纯化,将交叉污染的风险降至最低

产品详情

QIAamp DSP Virus Kit采用成熟和方便的QIAamp技术同时纯化病毒DNA和RNA。

绩效

使用QIAamp DSP Virus Kit纯化的病毒核酸可即用于各种敏感的下游应用,如基于酶的扩增或其他修饰,包括:PCR和RT-PCR。

原理

QIAamp DSP Virus Kit采用成熟和方便的QIAamp技术同时纯化病毒DNA和RNA。QIAamp硅胶膜特异性结合裂解样品中的核酸,其他裂解物通过真空操作去除。经过有效地洗涤去除污染物,然后洗脱DNA,洗脱体积为20 µl或60 µl。

程序

QIAamp DSP Virus Kit操作流程包括以下步骤:裂解、结合、洗涤(3x)、离心干燥和洗脱。使用真空抽滤装置,如QIAvac 24 Plus,从血浆或血清中纯化病毒核酸(参见"Procedure")。

应用

从血浆或血清样本中纯化病毒核酸。样本可加抗凝剂柠檬酸盐或EDTA,可以是新鲜的、或冷冻的(不可重复冻融)。

QIAamp DSP Virus Kit可纯化各种病毒核酸,与各种上游样品收集系统和下游应用兼容。

辅助数据和图表

Specifications

FeaturesSpecifications
ApplicationsZHPCR, RT-PCR, LCR
Elution volume20 µl, 60 µl
Main sample typeSerum, plasma
CE/FDA/IVD compatibleCE/IVD
FormatSample tubes
ProcessingManual (vacuum)
Purification of total RNA, miRNA, poly A+ mRNA, DNA or proteinViral DNA, viral RNA
Sample amount500 µl
TechnologySilica technology
YieldVaries

资源

安全数据表 (1)
Download Safety Data Sheets for QIAGEN product components.
产品介绍与指南 (1)
Certificates of Analysis (1)

FAQ

Does the QIAamp DSP Virus Kit require the QIAvac 24 Plus, or can I use it with my own laboratory vacuum system?
It is possible to use a general laboratory vacuum system with the QIAamp DSP Virus Kit. However, this will require validation in-house. The CE-marked QIAamp Kits have been developed, field-tested and validated with the QIAvac 24 Plus vacuum system (QIAvac 24 Plus, QIAvac Connecting System and Vacuum Pump). Using this system with the QIAamp DSP Virus Kit will avoid lengthy validation procedures for the enduser.
FAQ ID -789
What vacuum pressure should be applied using the QIAvac 24 Plus for the QIAamp DSP Virus Kit and Blood Mini Kit Protocols?

When processing samples with the QIAamp DSP DNA Blood Mini Kit and the QIAamp DSP Virus Kit, the vacuum pressure should be below -800 mbar. The QIAvac 24 Plus and the QIAvac Connecting System should be tested according to Appendix B of the QIAvac 24 Plus Handbook before performing a nucleic acid purification procedure.

If you would like to use an equivalent general laboratory vacuum system, make sure that the minimum vacuum pressure is reached. Performance of the QIAamp DSP DNA Blood Mini or Virus Kits in combination with a house-vacuum system has to be validated by the researcher.

FAQ ID -1033
What is the difference between QIAGEN Protease and QIAGEN Proteinase K provided in various QIAamp Kits?

QIAGEN Proteinase K is a subtilisin-type protease, which cleaves at the carboxyl side of hydrophobic, aliphatic and aromatic amino acids. It is particularly suitable for short digestion times. It possesses a high specific activity over a wide range of temperatures and pH values with substantially increased activity at higher temperature. Soluble calcium is not essential for enzymatic activity. This means that EDTA, which is used to inhibit Mg2+-dependent enzymes such as nucleases, will not inhibit Proteinase K activity.

QIAGEN Protease is a broad-specificity Serine protease with high activity, cleaving preferentially at neutral and acidic residues. It is an economical alternative to Proteinase K for isolation of native DNA and RNA from a variety of samples.

For more information on activity of QIAGEN Protease and Proteinase K in various buffers please click here.

FAQ ID -761
What can be used as an alternative to the A260 measurement for quantification of small amounts of RNA and DNA?

Small amounts of RNA and DNA may be difficult to measure spectrophotometrically. Fluorometric measurements, or quantitative RT-PCR and PCR are more sensitive and accurate methods to quantify low amounts of RNA or DNA.

Fluorometric measurements are carried out using nucleic acid binding dyes, such as RiboGreen® RNA Quantitation Reagent for RNA, and PicoGreen® DNA Quantitation Reagent for DNA (Molecular Probes, Inc.).

FAQ ID -728
What has to be done to an RNA sample before loading it onto an Agilent Bioanalyzer?

For RNA isolated on the BioRobot EZ1 and BioRobot M48:

The RNA can be directly applied to the Agilent Bioanalyzer, since it is being denatured in the final protocol steps of these isolation procedures.

For RNA prepared with all other QIAGEN RNA Isolation Products:

We recommend to denature the samples in a water bath for 2 min at 70°C, and then place them directly on ice prior to loading them onto the Agilent Bioanalyzer.

 

FAQ ID -528
How do I safely inactivate biohazardous flow-through material?

Always dispose of potentially biohazardous solutions according to your institution’s waste-disposal guidelines. Although the lysis and binding buffers in QIAamp, DNeasy, and RNeasy kits contain chaotropic agents that can inactivate some biohazardous material, local regulations dictate the proper way to dispose of biohazards. DO NOT add bleach or acidic solutions directly to the sample-preparation waste. Guanidine hydrochloride in the sample-preparation waste can form highly reactive compounds when combined with bleach.
Please access our Material Safety Data Sheets (MSDS) online for detailed information on the reagents for each respective kit.

FAQ ID -12