产品名称
Taq DNA聚合酶 来源于水生栖热菌, with 10× PCR reaction buffer without MgCl2
biological source
enzyme from bacterial (Thermus Aquaticus)
recombinant
expressed in E. coli
form
liquid
usage
sufficient for 1500 reactions
sufficient for 250 reactions
sufficient for 50 reactions
sufficient for 5000 reactions
feature
dNTPs included: no
hotstart: no
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
Quality Level
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Application
- DNA提取过程(基因扩增和测序过程)
- 基因分型
- 聚合酶链式反应(PCR),研究上皮中性粒细胞活化肽78 (ENA-78)和白细胞介素-8 (IL-8)的组成性产生
- 通过常规PCR扩增原代内皮细胞的RNA
Biochem/physiol Actions
Features and Benefits
- 在单独的试管中提供MgCl 2,以优化MgCl2。
- 可以耐受反复加热至95 °C而不出现明显活性损失。
General description
Legal Information
Other Notes
Packaging
hcodes
pcodes
Hazard Classifications
Aquatic Chronic 3
存储类别
12 - Non Combustible Liquids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
商品
Explore PCR's history, from discovery to Nobel Prize. Discover real-time PCR (qPCR) and digital PCR developments.
The polymerase chain reaction is one of the most widely used techniques in molecular biology. The PCR process consists of three main steps, Denaturation, Annealing & Extension
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。
聚合酶链反应是分子生物学应用最普遍的技术之一。PCR过程主要由三步组成:变性、退火和延伸
实验方案
Hot start dNTP protocol enhances specificity in PCR by blocking DNA polymerase nucleotide incorporation during PCR.
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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