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TAQuest qPCR Master Mix with Helixyte Green *低ROX*
货号 | 17272 | 存储条件 | 在零下15度以下保存, 避免光照 | |
规格 | 1 mL | 价格 | 1164 | |
Ex (nm) | Em (nm) | |||
分子量 | 溶剂 | Water | ||
产品详细介绍 |
简要概述
产品基本信息
货号:17272
产品名称:TAQuest qPCR Master Mix with Helixyte Green *低ROX*
规格:1ml
储存条件:-15℃避光防潮
保质期:12个月
产品物理化学光谱特性
溶剂:水
产品介绍
TAQuest qPCR Master Mix with Helixyte Green 是一种即用型 2X溶液,针对 qPCR 和 2 步 RT-qPCR 进行了优化。预混液在优化的 PCR 缓冲液中包含我们专有的 TAQuest 热启动 Taq DNA 聚合酶和 dNTP。您只需添加模板和目标引物即可运行所需的 PCR 反应。热启动 Taq DNA 聚合酶允许您在室温下设置 PCR 反应,从而最大限度地减少非特异性产物的形成。该酶与优化的缓冲液结合使用,可确保对所有样品类型(如基因组、质粒、病毒和 cDNA 模板)的 PCR 特异性和灵敏度。 Helixyte Green 嵌入染料无需使用序列特异性探针即可快速检测和分析DNA。该预混液包含少量 ROX 参考染料。金畔生物是AAT Bioquest的中国代理商,为您提供最优质的TAQuest qPCR Master Mix with Helixyte Green *低ROX*。
适用仪器
qPCR | |
仪器规格 | SYBR Green 滤波片 |
样品实验方案
注意 在室温下用 Helixyte Green *低ROX* 解冻 TAQuest™ qPCR Master Mix。 使用前彻底涡旋 qPCR Master Mix。
1. 制备表 1 所示的下列反应混合物之一。
2. 轻轻涡旋混合试剂,然后短暂离心。
3. 在 qPCR 仪器中设置板并按表 2 所示操作。
表 1. 各反应每孔试剂组成
成分 | 体积 (25 µL/reaction) | 体积 (50 µL/reaction) | 最终浓度 |
TAQuest qPCR Master Mix with Helixyte Green *低 ROX* | 12.5 µL | 25 µL | 1X |
上游引物,10 µM | 0.25-2.5 µL | 0.5-5.0 µL | 0.1-1.0 µM |
下游引物,10 µM | 0.25-2.5 µL | 0.5-5.0 µL | 0.1-1.0 µM |
DNA模板 | 1-5 µL | 1-5 µL | 优化的浓度 |
无核酸酶水 | 25 µL | 50 µL |
表 2. 热循环参数
范围 | 聚合酶激活 | PCR (30-40个循环) | ||
Hold | 变性 | 退火 | 延伸 | |
温度 | 95 °C | 95 °C | 55-65 °C | 68-72 °C |
时间 (m:ss) | 0:20 | 0:30 | 1:00 | 1:00 |
参考文献
A SYBR Green I-based real-time polymerase chain reaction assay for detection and quantification of canine bufavirus.
Authors: Wang, Yong and Sun, Jianfei and Guo, Xu and Li, Wei and Zhang, Da and Liu, Guangqing and Zhou, Tianhong and Li, Yongdong
Journal: Molecular and cellular probes (2021): 101762
A duplex SYBR green I-based real-time polymerase chain reaction assay for concurrent detection of feline parvovirus and feline coronavirus.
Authors: Sun, Liting and Xu, Zhiqing and Wu, Junhuang and Cui, Yongqiu and Guo, Xu and Xu, Fazhi and Li, Yongdong and Wang, Yong
Journal: Journal of virological methods (2021): 114294
A new SYBR Green real-time PCR to detect SARS-CoV-2.
Authors: Marinowic, D R and Zanirati, G and Rodrigues, F V F and Grahl, M V C and Alcará, A M and Machado, D C and Da Costa, J C
Journal: Scientific reports (2021): 2224
A novel duplex SYBR Green real-time PCR with melting curve analysis method for beef adulteration detection.
Authors: Li, Jiapeng and Wei, Yixuan and Li, Jinchun and Liu, Ruixi and Xu, Suigen and Xiong, Suyue and Guo, Ya and Qiao, Xiaoling and Wang, Shouwei
Journal: Food chemistry (2021): 127932
A rapid and low-cost protocol for the detection of B.1.1.7 lineage of SARS-CoV-2 by using SYBR Green-based RT-qPCR.
Authors: Abdel Sater, Fadil and Younes, Mahmoud and Nassar, Hassan and Nguewa, Paul and Hamze, Kassem
Journal: Molecular biology reports (2021): 7243-7249
Design and characterization of a SYBR Green I-based melting curve method for investigation of HER2I655V polymorphism in breast cancer.
Authors: Desriani and Azamris and Ghaissani, Shabrina S and Kinanti, Senja R and Warisman, Muhammad A and Fitria, N
Journal: Journal, genetic engineering & biotechnology (2021): 6
Development and Validation of a SYBR Green Real Time PCR Protocol for Detection and Quantification of Nervous Necrosis Virus (NNV) Using Different Standards.
Authors: Olveira, José G and Souto, Sandra and Bandín, Isabel and Dopazo, Carlos P
Journal: Animals : an open access journal from MDPI (2021)
Development and application of SYBR Green Ⅰ real-time quantitative reverse transcription PCR assay for detection of swine Getah virus.
Authors: Xia, Yin-He and Shi, Zi-Cong and Wang, Xin-Wei and Li, Yong-Tao and Wang, Zeng and Chang, Hong-Tao and Liu, Hong-Ying and Chen, Lu and Wang, Chuan-Qing and Yang, Xia
Journal: Molecular and cellular probes (2021): 101730
Development of New PCR Assay with SYBR Green I for Detection of Mycoplasma, Acholeplasma, and Ureaplasma sp. in Cell Cultures.
Authors: Krzysztoń-Russjan, Jolanta and Chudziak, Jakub and Bednarek, Małgorzata and Anuszewska, Elżbieta Lidia
Journal: Diagnostics (Basel, Switzerland) (2021)
Development of SYBR Green I-based polymerase chain reaction for feline bocavirus 1 detection.
Authors: Wang, Yong and Li, Wei and Guo, Xu and Zhang, Da and Sun, Jianfei and Fu, Ziteng and Liu, Guangqing and Li, Yongdong and Jiang, Shudong
Journal: 3 Biotech (2021): 61