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AugeGreenTM qPCR Master Mix
Product overview:
Product content
Component |
100T |
500T |
A. 2 × AugeGreenTM Master Mix |
1 mL |
5×1 mL |
B. 10 × ROX reference dye |
0.5 mL |
1 mL |
Spectral Properties of Super EvaGreen Dye:
The absorption and fluorescence emission spectra of DNA- bound Super EvaGreen dye are very similar to those of SYBR Green I or FAM.
λabs/λem = 500/530 nm (DNA bound)
λabs = 471 nm (without DNA)
Storage and Handling
AugeGreenTM qPCR Master Mix is shipped on blue ice and should be stored immediately upon arrival at -20℃. When stored under the recommended condition and handled correctly, the kit should be stable for at least 12 months from the date of receipt. Before use, thaw the product at room temperature (warm up directly without ice) and gently vortex to mix. Uneven mixing of reagents can result in poor experimental results. After thawing, all experiments should be performed on ice. The product can be refrigerated for storage.
Product Description
AugeGreenTM qPCR Master Mix is a ready-to-use hot-start mix for qPCR and DNA melt curve analysis of PCR amplicons. It is formulated for qPCR using a fast cycling protocol, but also can be used for qPCR with regular cycling protocols.
AugeGreenTM dye is a unique DNA-binding dye with features ideal for both qPCR and melt curve analysis. AugeGreenTM dye binds to dsDNA via a novel “release-on-demand” mechanism, which permits the use of a relatively high dye concentration in qPCR without PCR inhibition.
AugeGreenTM qPCR Master Mix contains our proprietary chemically-modified UE hot-start Taq DNA Polymerase. Unlike AmpliTaq Gold, which is also a chemically modified Taq but takes 10 minutes or longer to activate, this UE Taq DNA Polymerase is fully activated in 2 minutes with high activity recovery, making it particularly suitable for fast PCR. UE HS-Taq is completely inactive at room temperature and largely free of DNA contamination. This makes UE HS-Taq superior to any antibody-based hot-start Taq, which is typically not completely inactive at room temperature and is prone to DNA contamination due to the nature of antibody production.
A unique feature of AugeGreenTM dye is its safety. DNA-binding dyes are inherently dangerous due to their potential to cause mutation. With this in mind, our scientists designed AugeGreenTM dye such that it cannot cross cell membranes, thus preventing the dye from being in contact with genomic DNA in live cells. All other commercial PCR dyes enter into cells in a matter of minutes. SYBR Green I, for example, has been shown to be environmentally more toxic than ethidium bromide, a well-known mutagen.
An added benefit of AugeGreenTM Master Mix is that you can analyze your PCR product by gel electrophoresis without the need to add another DNA-binding dye to either your loading buffer or gel. The SAugeGreenTM dye in the Master Mix can act as a DNA prestain, permitting direct visualization of DNA bands following electrophoresis.
Citations and references:
Meng, Chengsheng Yan, Yuanyuan Liu, Zhengwen Chen, Liting Zhang, Yan Li, Xiuxin Wu, Liqiang Zhang, Guiyin Wang, Xingfen Ma, Zhiying
Frontiers in Plant Science (2018)
Zenda, Tinashe Liu, Songtao Wang, Xuan Jin, Hongyu Liu, Guo Duan, Huijun
International Journal of Molecular Sciences (2018)
张建平,王昭玉,苏智,魏建荣,刘建凤
分子植物育种(2019)
侯胜奎 陶晨雨 胡慧艳 刘津 李志强 张婧 贾青
中国畜牧杂志(2019)
Youbin Kong, Bing Wang, Hui Du,Wenlong Li, XiHuan Li, Caiying Zhang
Frontiers in Plant Science (05 July 2019)
Xuan Wang, Tinashe Zenda , Songtao Liu, Guo Liu, Hongyu Jin, Liang Dai,Anyi Dong, Yatong Yang and Huijun Duan
Int. J. Mol. Sci. 2019, 20(15), 3743
王昭玉 封润霞 苏智 魏建荣 李臻 刘建凤
分子植物育种
Zhaoyu Wang, Runxia Feng, Xue Zhang, Zhi Su, Jianrong Wei, Jianfeng Liu
Genome, 2019, 62(10): 689-703
Zhiming Hao,Miaomiao Geng,Yanran Hao,Yue Zhang,Lijing Zhang,Shumin Wen,Ruihui Wang,Guiru Liu
Theoretical and Applied Genetics November 2019, Volume 132, Issue 11, pp 3201–3221
Jie Liu,Liucheng Wang,Guona Zhou,Suhong Gao,Tianhua Sun,Junxia Liu,Baojia Gao
Arch Insect Biochem Physiol.
Songtao Liu,Tinashe Zenda,Anyi Dong,Yatong Yang,Xinyue Liu,Yafei Wang,Jiao Li,Yongsheng Tao,Huijun Duan
Int. J. Mol. Sci. 2019, 20(22), 5586
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