제품 이름
Taq DNA Polymerase from Thermus aquaticus, with 10× PCR reaction buffer containing MgCl2
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
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
- in the quantification of fungal growth by polymerase chain reaction (PCR) and photometric assay
- in conventional reverse transcriptase (RT)-PCR
- in simple sequence repeats (SSR) genotyping
- as a component of PCR mix for amplification of genomic and mitochondrial DNA
- in direct tetra-primer amplification refractory mutation system (T-ARMS) PCR to amplify dried whole blood samples
Biochem/physiol Actions
Features and Benefits
- Low per unit cost of Taq
General description
Legal Information
Other Notes
Packaging
저장 등급
12 - Non Combustible Liquids
문서
Explore PCR's history, from discovery to Nobel Prize. Discover real-time PCR (qPCR) and digital PCR developments.
프로토콜
표준 PCR 프로토콜 단계를 알아보고 시약 목록 또는 사이클링 매개변수를 검토하세요. 일상적인 DNA 증폭을 위한 이 방법은 표준 Taq DNA 중합효소를 사용합니다.
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.
자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..
고객지원팀으로 연락바랍니다.