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  • AugeGreenTM qPCR Master Mix

    Product No.:S2008

    Product specification:20μL×100T/20μL×500T

    Catalogue price(RMB):500/1000

    Can replace similar products:qPCR SYBR Green Master Mix

    Bulk Request


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

The product contains two components. Component A contains Super EvaGreen dye, dNTP, PCR buffer (including Tris and MgCl2) and hot-start Taq polymerase. Component B is 10× Rox reference, which may be required on certain ABI instruments (See protocol below).


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.


Instructions:


   UE-S2008

Citations and references:


1.Systematic Analysis of Cotton Non-specific Lipid Transfer Protein Family Revealed a Special Group That Is Involved in Fiber Elongation

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)

2.Comparative Proteomic and Physiological Analyses of Two Divergent Maize Inbred Lines Provide More Insights into Drought Stress Tolerance Mechanisms

Zenda, Tinashe Liu, Songtao Wang, Xuan Jin, Hongyu Liu, Guo Duan, Huijun

International Journal of Molecular Sciences (2018)

3.沙棘转录因子基因HrWRKY1的克隆与表达分析

张建平,王昭玉,苏智,魏建荣,刘建凤

分子植物育种(2019)

4.牛性控精液纯度快速评价方法研究

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)

5.GmEXLB1, a Soybean Expansin-Like B Gene, Alters Root Architecture to Improve Phosphorus Acquisition in Arabidopsis

Youbin Kong, Bing Wang, Hui Du,Wenlong Li, XiHuan Li, Caiying Zhang

Frontiers in Plant Science (05 July 2019)

6.Comparative Proteomics and Physiological Analyses Reveal Important Maize Filling-Kernel Drought-Responsive Genes and Metabolic Pathways

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

7.沙棘HrCYP85A1基因生物信息及表达分析

王昭玉 封润霞 苏智 魏建荣 李臻 刘建凤

分子植物育种

8.Characterization of the Hippophae rhamnoides WRKY gene family and functional analysis of the role of the HrWRKY21 gene in resistance to abiotic stresses

Zhaoyu Wang, Runxia Feng, Xue Zhang, Zhi Su, Jianrong Wei, Jianfeng Liu

Genome, 2019, 62(10): 689-703

9.Screening for differential expression of genes for resistance to Sitodiplosis mosellana in bread wheat via BSR‑seq analysis

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

10.Midgut transcriptome analysis of Clostera anachoreta treated with lethal and sublethal Cry1Acprotoxin

Jie Liu,Liucheng Wang,Guona Zhou,Suhong Gao,Tianhua Sun,Junxia Liu,Baojia Gao

Arch Insect Biochem Physiol. 

11.Comparative Proteomic and Morpho-Physiological Analyses of Maize Wild-Type Vp16 and Mutant vp16 Germinating Seed Responses to PEG-Induced Drought Stress

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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