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Merck

R1028

Sigma-Aldrich

Restorase® DNA Polymerase with 10× Reaction Buffer

Enzyme blend for PCR amplification of damaged DNA

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About This Item

分類程式碼代碼:
12352202
NACRES:
NA.55

品質等級

形狀

liquid

用途

sufficient for 50 reactions

特點

Long & Accurate PCR
dNTPs included: no
hotstart: no

濃度

2.5 units/μL

技術

PCR: suitable

顏色

colorless

輸入

purified DNA

運輸包裝

wet ice

儲存溫度

−20°C

一般說明

Restorase DNA Polymerase with 10× Reaction Buffer combines Sigma′s long and accurate enzyme technology with a small amount of DNA repair enzyme. The optimized blend will initiate the repair and further amplification of damaged DNA templates greater than 800 bp. Restorase has also been shown to increase yield on undamaged DNA templates.

應用

Restorase® DNA Polymerase with 10× Reaction Buffer has been used in DNA repair.

生化/生理作用

DNA templates are often damaged on exposure to heat, acids, alkylating agents, and light. These damaged templates result in inefficient or failed DNA amplification by polymerase chain reaction (PCR). Restorase® DNA Polymerase repairs the damaged sites on the DNA templates and initiates subsequent template copying. Restorase treatment of the DNA depends on the level of template damage.

特點和優勢

  • Reliable amplification of damaged DNA
  • When thermostable polymerases fail, this enzyme amplifies the sequence efficiently
  • Efficient amplification of sequences in multiplex reactions
  • Increased yield and amplicon specificity
  • Amplifies a broad spectrum of amplicon sizes varying from 200 bp to 20 kb
  • Can repair 3′ bungs, nicks, and abasic sites

包裝

The enzyme is provided with an optimized 10× reaction buffer provided as 1 vial/250 units.

其他說明

Learn more about our offering of specialty enzymes at www.sigma-aldrich.com/specialtyenzymes.
View more detailed information on Restorase DNA Polymerase at www.sigma-aldrich.com/restorase.

法律資訊

本产品的使用受到如下一项或多项美国专利及其对应的境外专利声明保护:5,789,224, 5,618,711, 6,127,155以及与届满的美国专利号5,079,352对应的境外专利声明。购买本产品,即相当于依照境外的专利声明获得了一份受限制、不可转让的使用许可,即将此等数量的产品用于购买者内部的研究用途。我们未明确表示、暗示或以禁止反言的形式授予您任何其他专利声明下的权利、进行任何专利方法申请的权利、进行任何形式的商业服务的权利,包括但不限于出于收费或其他商业考虑而报告购买者的研究活动结果的权利。本产品仅适合于研究用途。如需用于Roche专利许可的诊断用途,需另外征得Roche许可。有关购买许可的更多信息,可联系Director of Licensing, Applied Biosystems, 850 Lincoln Centre Drive, Foster City, California 94404, USA获取。
Restorase is a registered trademark of Merck KGaA, Darmstadt, Germany

危險聲明

防範說明

危險分類

Aquatic Chronic 3

儲存類別代碼

10 - Combustible liquids


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Francesca Zinetti et al.
PloS one, 8(6), e65746-e65746 (2013-06-12)
There is increasing evidence that most parapatric cryptic/sister taxa are reproductively compatible across their areas of contact. Consequently, the biological species concept, which assumes absence of interbreeding, is becoming a not so effective criterion in evolutionary ecology. Nevertheless, the few
Mehrdad Hajibabaei et al.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 360(1462), 1959-1967 (2005-10-11)
Large-scale DNA barcoding projects are now moving toward activation while the creation of a comprehensive barcode library for eukaryotes will ultimately require the acquisition of some 100 million barcodes. To satisfy this need, analytical facilities must adopt protocols that can
Innis, M.A., et al.
PCR Protocols: A Guide to Methods and Applications (1990)
James M Robertson et al.
Forensic science international. Genetics, 12, 168-180 (2014-07-06)
Forensic scientists have used several approaches to obtain short tandem repeat (STR) profiles from compromised DNA samples, including supplementing the polymerase chain reaction (PCR) with enhancers and using procedures yielding reduced-length amplicons. For degraded DNA, the peak intensities of the
Shigeo Yagi et al.
Parasitology research, 102(2), 211-217 (2007-09-28)
Granulomatous amoebic encephalitis (GAE) is a usually fatal disease caused by the free-living amoebae Balamuthia mandrillaris and Acanthamoeba spp. The intent of this study was to determine if the polymerase chain reaction (PCR) could be used retrospectively to detect amoeba

商品

Restorase® DNA Polymerase

实验方案

Method for amplification of DNA from damaged DNA sources. Particularly useful for DNA extracted from old samples.

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