Merck
CN

P0982

Sigma-Aldrich

JumpStart REDTaq® ReadyMix 反应混合物

for PCR

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别名:
Hot start PCR master mix, Hot start master mix, Hot start taq master mix
MDL编号:

质量水平

形式

liquid

用途

sufficient for 100 reactions
sufficient for 20 reactions
sufficient for 800 reactions

特点

dNTPs included
hotstart

浓度

2.5 units/reaction (50 μL reaction volume)

技术

PCR: suitable

颜色

red

输入

purified DNA

应用

agriculture

运输

wet ice

储存温度

−20°C

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一般描述

JumpStart REDTaq ReadyMix PCR反应混合物是制备好的溶液,结合了热启动PCR的性能优势和Sigma ReadyMix和REDTaq的双重便利性。反应混合物优化的2x反应浓缩物中包括Sigma的JumpStart Taq DNA聚合酶、99%纯度的脱氧核苷酸、缓冲液和惰性红色染料。将25 μL ReadyMix加到引物、模板和水中,使最终反应体积为50 μL。在室温下,反应混合物中的JumpStart Taq抗体可使Taq DNA聚合酶失活。在PCR的第一次变性步骤期间,复合物解离,聚合酶活性完全恢复。惰性红色染料不影响自动测序、限制性酶切、连接或其他下游操作。如果需要,只需通过标准纯化方法就可将PCR产物与染料轻松分离。热启动机制允许设置室温,使其成为高通量应用的理想选择 。

应用

Jumpstart REDTaq® ReadyMix反应混合物可用于直接提取DNA并进行PCR扩增。还用于:
  • 多重定量PCR
  • 甲基化特异性PCR(MSPCR)
  • 总RNA合成cDNA的PCR扩增

特点和优势

  • JumpStart REDTaq® DNA聚合酶是一种抗体失活的热启动酶,旨在最大限度地减少非特异性扩增,同时提高目标产量和特异性
  • 无论模板浓度如何,JumpStart Taq DNA聚合酶均可提供优越的扩增效果
  • REDTaq JumpStart ReadyMix可减少移液步骤,降低污染风险。 热启动机制允许设置室温,使其成为高通量应用的理想选择 。
  • 惰性红色染料方便验证试剂是否适当混合
  • 不需要装载其他染料。可以在反应后将等分试样直接加载到琼脂糖凝胶上

包装

默认的反应体积为50 μL

20RXN包装成1 X 500 μL
100RXN包装成1 X 2.5 mL
800RXN包装成1 X 20 mL

单位定义

在74℃下,一个单位可在30分钟内将10 nM总dNTP掺入酸可沉淀的DNA中。

其他说明

想查看JumpStart REDTaq和ReadyMix产品的更多详细信息,请访问 www.sigma-aldrich.com/hotstart
对于典型的PCR反应,将25 μL JumpStart REDTaq® ReadyMix反应混合物与25 μL混合物(含有模板DNA、引物和水)混合。可根据需要改变反应体积。

法律信息

凡购买本产品,即表示授权用户使用产品说明书所指定的专利,但仅限于将所购数量的产品用于内部研究用途。我们未明确表示、暗示,或通过禁止反言形式转让任何其他专利权(如,5′ Nuclease Process专利权)。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。
依照美国专利号5,338,671和5,587,287和其他地区对应的专利,许可抗体用于体外研究用途。
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:US 8,404,464和US 7,972,828。 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。
JumpStart is a trademark of Sigma-Aldrich Co. LLC
REDTaq is a registered trademark of Merck KGaA, Darmstadt, Germany
ReadyMix is a trademark of Sigma-Aldrich Co. LLC

法规信息

常规特殊物品
含少量动物源组分生物产品

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Nijiro Nohata et al.
Developmental biology, 411(2), 183-194 (2016-02-14)
Angiogenesis, the formation of new blood vessels by remodeling and growth of pre-existing vessels, is a highly orchestrated process that requires a tight balance between pro-angiogenic and anti-angiogenic factors and the integration of their corresponding signaling networks. The family of
Stephen J Murphy et al.
DNA research : an international journal for rapid publication of reports on genes and genomes, 19(5), 395-406 (2012-09-20)
High-throughput next-generation sequencing provides a revolutionary platform to unravel the precise DNA aberrations concealed within subgroups of tumour cells. However, in many instances, the limited number of cells makes the application of this technology in tumour heterogeneity studies a challenge.
Stephen J Murphy et al.
Gastroenterology, 145(5), 1098-1109 (2013-08-06)
Increasing grade of pancreatic intraepithelial neoplasia (PanIN) has been associated with progression to pancreatic ductal adenocarcinoma (PDAC). However, the mechanisms that control progression from PanINs to PDAC are not well understood. We investigated the genetic alterations involved in this process. Genomic
Wendy Monger et al.
Archives of virology, 163(6), 1585-1594 (2018-03-02)
A novel virus was discovered in a freeze-dried collection held at SASA, UK, originating from potato (Solanum tuberosum) cv. Nadine. The complete sequence of the viral RNA was determined to be 3674 nucleotides in length encoding five predicted proteins. Based
Tatiana V Danilova et al.
Chromosoma, 121(6), 597-611 (2012-10-12)
Fluorescence in situ hybridization (FISH) is a useful tool for physical mapping of chromosomes and studying evolutionary chromosome rearrangements. Here we report a robust method for single-copy gene FISH for wheat. FISH probes were developed from cDNA of cytosolic acetyl-CoA

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实验方案

介绍RedTaq的应用和优势,包括用于基因组DNA PCR的标准RedTaq、热启动RedTaq和RedTaq。

Reviews the applications and benefits for RedTaq, including standard RedTaq, Hot Start RedTaq and RedTaq for genomic DNA PCR.

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