추천 제품
Quality Level
형태
liquid
사용
sufficient for 100 reactions
sufficient for 400 reactions
특징
Multiplex PCR
dNTPs included
hotstart
농도
2.5 units/reaction (50 μL reaction volume)
기술
PCR: suitable
색상
colorless
적합성
suitable for (quantitative PCR)
응용 분야
agriculture
배송 상태
wet ice
저장 온도
−20°C
일반 설명
애플리케이션
- For PCR amplifications that require reduced non-specific amplification
- For multiplex PCR
- For reduction of primer dimers
특징 및 장점
- The master mix allows consistency from one reaction to the next
- Reduced preparation time and reduced risk of contamination from multiple pipetting steps
- Designed to minimize non-specific amplification and contamination
- Increased specificity and target yield
- Reduced primer dimers
- Reduced set-up time as compared to manual or wax Hot Start methods
- Allows for room temperature set-up
- Ideal for high throughput, quantitative PCR applications
포장
100RXN is packaged as 1 X 2.5 mL
400RXN is packaged as 1 X 10 mL
기타 정보
This product has been validated in quantitative PCR, but may require supplementation with magnesium chloride solution, 25 mM, Catalog Number M8787, a suitable fluorescent probe, and, if desired, an internal reference dye, Catalog Number R4526. View more detailed information on JumpStart Taq ReadyMix products at www.sigma-aldrich.com/hotstart.
법적 정보
관련 제품
Storage Class Code
10 - Combustible liquids
WGK
WGK 2
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
문서
Method outlines use of a hot start Taq for multiplex qPCR and provides guidance on how to optimize dNTPs, primer, probes and MgCL2 concentrations. By optimizing these parameters, the user can improve assay sensitivity and linear range of detection.
Learn about the history of the polymerase chain reaction (PCR), from the basic principles that proceeded its discovery to the awarding of a Nobel Prize for Chemistry and more recent developments such as real-time PCR (qPCR) and digital PCR.
The purpose of Hot Start PCR is to inhibit the PCR reaction in order to reduce nonspecific amplification, prevent the formation of primer dimers, and increase product yields.
프로토콜
The CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) system was discovered in bacteria, where it functions as an adaptive immune system against invading viral and plasmid DNA.
Protocol using antibody mediated hot start polymerase. Method has short activation period (<1min), and results in higher yields and more specificity over standard PCR methods.
When using hot start Taq DNA polymerase, the enzyme remains inactive until heated. Hot Start DNA polymerase control is achieved by chemical or antibody modification of the enzyme.
자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..
고객지원팀으로 연락바랍니다.