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About This Item
Quality Level
usage
sufficient for 250 reactions
feature
dNTPs included, hotstart
technique(s)
qPCR: suitable, RT-qPCR: suitable
color
colorless
input
purified RNA
compatibility
ABI 5700, ABI 7000, ABI 7300, ABI 7500 Fast, ABI 7500, ABI 7700, ABI 7900 HT , ABI 7900 HT Fast, ABI 7900, ABI StepOne, ABI StepOnePlus, ABI ViiA 7, Bio-Rad CFX384, Bio-Rad CFX96, Bio-Rad MJ Chromo4, Bio-Rad MJ Opticon 2, Bio-Rad MJ Opticon, Bio-Rad MiniOpticon, Bio-Rad MyiQ, Bio-Rad iCycler iQ, Bio-Rad iQ5, Cepheid SmartCycler, Eppendorf® Mastercycler ep realplex2 s, Eppendorf® Mastercycler ep realplex, Illumina Eco qPCR, Qiagen Corbett Rotor-Gene 3000, Qiagen Corbett Rotor-Gene 6000, Qiagen Corbett Rotor-Gene Q, Roche LightCycler 480, Strategene Mx3000P, Strategene Mx3005P, Strategene Mx4000
detection method
SYBR® Green
shipped in
wet ice
storage temp.
−20°C
General description
Application
- to detect specific genetic clusters of genogroup I and II noroviruses
- for chikungunya viral (CHIKV) RNA quantification
- to detect mRNA expression levels
- for amplification of total RNA extracted from human umbilical vein endothelial cells (HUVECs) and prostate cancer cells
Features and Benefits
- The master mix allows consistency and reproducibility from one reaction to the next
- Reduced preparation time and the risk of contamination from multiple pipetting steps
- Reduced set-up time as compared to manual or wax Hot Start methods
- JumpStart™Taq Polymerase reduces primer-dimer and non-specific product formation
- SYBR® Green I dye is inexpensive, easy to use, and highly sensitive
- Broad instrument compatibility
- Includes a separate ROX reference dye vial for reaction normalization
Packaging
Legal Information
Kit Components Only
- SYBR® Green Taq ReadyMix™ for Quantitative RT-PCR 2 x 25
signalword
Danger
Storage Class
8A - Combustible corrosive hazardous materials
flash_point_f
Not applicable
flash_point_c
Not applicable
wgk
WGK 3
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - ED ENV 1 - Eye Dam. 1 - Skin Corr. 1C - Skin Sens. 1
Regulatory Information
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Protocols
使用逆转录酶和dNTPs进行逆转录(RT)使用总RNA或基因特异性方法实现仅目标RNA被转化为cDNA。
引物浓度优化实验方案是一种建立反应阵列的方法。该阵列用来对照伴侣引物的不同浓度来测试每种引物的一系列浓度。
Perform reverse transcription (RT) using a reverse transcriptase enzyme and dNTPs. Use total RNA or a gene-specific approach so that only the RNA of interest is converted to cDNA.
Articles
分析基因表达的方法之一是测量基因的mRNA浓度。此类分析面临着若干挑战,例如不同转录本之间的半衰期不同、转录时间模式以及mRNA和蛋白质之间缺乏相关性。
Challenges in gene expression analysis include mRNA stability, temporal transcription patterns, and mRNA-protein correlation, impacting accuracy.
PCR master mix simplifies PCR/RT-PCR with components like DNA polymerase, dNTPs, MgCl2, and buffer, available commercially or DIY.
Related Content
RT-qPCR detects specific targets with applications in gene expression and pathogen detection.
Global Trade Item Number
| SKU | GTIN |
|---|---|
| QR0100-1KT | 04061835378371 |


