选择尺寸
关于此项目
biological source
enzyme from bacterial (Thermus Aquaticus)
recombinant
expressed in E. coli
form
liquid
usage
sufficient for 10000 reactions, sufficient for 3000 reactions, sufficient for 500 reactions
mol wt
94 kDa
feature
dNTPs included: no, hotstart: no, Standard PCR
Quality Level
concentration
5 units/μL
technique(s)
PCR: suitable
color
colorless
input
purified DNA
suitability
suitable for PCR and automated sequencing reactions
application(s)
agriculture
shipped in
wet ice
storage temp.
−20°C
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General description
Application
- 通过聚合酶链反应(PCR)和光度法定量真菌生长
- 传统逆转录酶(RT)-PCR
- 简单序列重复(SSR)基因分型
- 作为PCR混合物的成分,用于基因组和线粒体DNA的扩增
- 用直接四引物扩增难降解突变系统(T-ARMS) PCR扩增干燥全血标本
Biochem/physiol Actions
Features and Benefits
- Taq的单位成本较低
Packaging
Other Notes
Legal Information
存储类别
12 - Non Combustible Liquids
wgk
WGK 3
法规信息
商品
Explore PCR's history, from discovery to Nobel Prize. Discover real-time PCR (qPCR) and digital PCR developments.
了解聚合酶链反应(PCR)的历史,从促进它的发现的基本原理到获得诺贝尔化学奖,以及实时PCR(qPCR)和数字PCR等最近的发展。
实验方案
Hot Start dNTPs block DNA polymerase until heat activation, enhancing PCR specificity.
Learn standard PCR protocol steps and review reagent lists or cycling parameters. This method for routine PCR amplification of DNA uses standard Taq DNA polymerase.
了解标准 PCR 方案步骤,查看试剂清单或循环参数。本方法使用标准 Taq DNA 聚合酶对 DNA 进行常规 PCR 扩增。
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