![SMOBIO/[TQ1110] ExcelTaq™ 2X Q-PCR Master Mix (SYBR, ROX), 200 Rxn/SYBR, ROX), 200 Rxn</span>
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Description
The ExcelTaq™ 2X Q-PCR Master Mix (SYBR, ROX) is a ready-to-use reagent with all the essential components for quantitative real-time PCR (qPCR) except primers and template. The master mix features high sensitivity (Fig. 1) and high signal intensity when compared with Brand A (Fig. 2). The ExcelTaq™ 2X Q-PCR Master Mix (SYBR, ROX) contains hot-start Taq polymerase in an optimized buffer with dsDNA specific SYBR green fluorescent dye. This master mix allows for sensitive and precise amplification, real-time tracking of the amplification process, and simultaneous quantification for targeted DNA molecules. The master mix includes ROX reference dye for normalization of each qPCR assay. With inert smart blue contrast dye, the ExcelTaq™ 2X Q-PCR Master Mix (SYBR, ROX) is ready-to-use and greatly reduces pipetting errors, while largely improving the reproducibility of the process.
Features
High sensitivity and signal intensity
With ROX reference dye
Smart blue contrast dye as a visual aid for reaction setup
Better compatibility for reverse transcription
Storage
Protected from light. Aliquot to avoid multiple freeze-thaw cycles.-20°C for 12 months
High sensitivity
The amplification plot of real-time PCR with cDNA templates ranging from 1.49 fg to 25 ng in quantity, analyzed by using TQ1110 ExcelTaq™ 2X Q-PCR Master Mix (SYBR, ROX) for qPCR amplification.
Better fluorescent signal
SMOBIO’s TQ1110 ExcelTaq™ 2X Q-PCR Master Mix (SYBR, ROX) shows better fluorescent signal as compared to a similar product (Brand A).
Contents
Component | Volume | Cat. No |
ExcelTaq™ 2X Q-PCR Master Mix (SYBR, ROX) | 2 x 1 ml | TQ1110 (200 Rxn) |
Storage
Protected from light. Aliquot to avoid multiple freeze-thaw cycles.-20°C for 12 months
Manual
Manual_TQ1110_ExcelTaq™ 2X Q-PCR Master Mix (SYBR, ROX)
SDS
SDS_TQ1110
Flyer
SMOBIO’s Q-PCR Master Mix- Instrument Compatibility
TaqMan® vs. SYBR® Green Chemistry
How can I choose ExcelTaq™ 2X Q-PCR Master Mix?
What instruments are compatible with ExcelTaq™ 2X Q-PCR Master Mix ?
Product Name | ExcelTaq™ 2X Q-PCR Master Mix (SYBR, no ROX) | ExcelTaq™ 2X Q-PCR Master Mix (SYBR, ROX) | ExcelTaq™ 2X Fast Q-PCR Master Mix (SYBR, no ROX) | ExcelTaq™ 2X Fast Q-PCR Master Mix (SYBR, ROX) | ExcelTaq™ 2X Q-PCR Master Mix (TaqMan, ROX) |
Cat. No. | TQ1100 | TQ1110 | TQ1200 | TQ1210 | TQ2110 |
Detection chemistry | SYBR | SYBR | SYBR | SYBR | TaqMan |
Blue contrast dye for best convenience | ü | ü | ü | ü | X |
ROX dye for reference | X | ü | X | ü | ü |
Time required for enzyme activation | 10 min | 10 min | 2 min | 2 min | 10 min |
qPCR program | Standard | Standard | Fast and Standard | Fast and Standard | Standard |
Instrument Compatibility* | |||||
Applied Biosystems system: | |||||
5700, 7000, 7300, 7700, and 7900HT | Δ | V | Δ | V | V |
StepOne, StepOnePlus | Δ | V | Δ | V | V |
7500, 7500 Fast, QuantStudio, ViiA7 | Δ | Δ | Δ | Δ | Δ |
BioRad system: | |||||
CFX96 , CFX384 | V | V | V | V | V |
iQ5 | V | V | V | V | V |
Opticon, Opticon 2, Chromo 4 | V | V | V | V | V |
Cepheid system: | |||||
Smart Cycler | V | V | V | V | V |
Eppendorf system: | |||||
Mastercycler ep realplex | V | V | V | V | V |
Roche system: | |||||
LightCycler 480, Nano | V | V | V | V | V |
QIAgen system: | |||||
Rotor-Gene™ 3000, 6000, Q | V | V | V | V | V |
Agilent (Stratagene) system: | |||||
MX3000P, 3005P, 4000P | Δ | Δ | Δ | Δ | Δ |
Illumina system: | |||||
Eco | V | V | V | V | V |
Can you provide the results that using ExcelTaq™ 2X Q-PCR Master Mix (SYBR, ROX, TQ1110) with different instruments?
Reference Gene Selection in Phenacoccus solenopsis Tinsley (Hemiptera: Pseudococcidae) and Their Normalization Impact on Gene Expression in RNAi Studies.
Satnam Singh Suneet Pandher Mridula Gupta Gurmeet Kaur Pankaj Rathore
Journal of Economic Entomology, toy328, Published: 17 October 2018 doi: 10.1093/jee/toy328
Synergistic inhibition effect of TNIK inhibitor KY-05009 and receptor tyrosine kinase inhibitor dovitinib on IL-6-induced proliferation and Wnt signaling pathway in human multiple myeloma cells
Yura Lee, Jung-Il Jung, Kyeong-Yong Park, Soon Ae Kim, Jiyeon Kim Oncotarget. 2017 Jun 20; 8(25): 41091–41101. Published online 2017 Apr 12. doi: 10.18632/oncotarget.17056
PMCID: PMC5522218
Hydroxylation and sulfation of sex steroid hormones in inflammatory liver
Sang R. Lee, Seung-yeon Lee, Sang-yun Kim, Si-yun Ryu, Bae-kuen Park, Eui-Ju Hong J Biomed Res. 2017; 31(5): 437–444. doi: 10.7555/JBR.31.20170031
PMCID: PMC5706436
Loss of endogenous estrogen increases cardiac toxicity by doxorubicin
Young Ho Lee, Sang R. Lee, Sun Woo Kwon, Seung-yeon Lee, Bae-kuen Park, Eui-Ju Hong
Journal of Biomedical Translational Research Vol.18 No.4 pp.146-150 DOI : https://doi.org/10.12729/jbtr.2017.18.4.146
ExcelTaq™ 2X Q-PCR Master Mix
Product Name | ExcelTaq™ 2X Q-PCR Master Mix (SYBR, no ROX) | ExcelTaq™ 2X Q-PCR Master Mix (SYBR, ROX) | ExcelTaq™ 2X Fast Q-PCR Master Mix (SYBR, no ROX) | ExcelTaq™ 2X Fast Q-PCR Master Mix (SYBR, ROX) | ExcelTaq™ 2X Q-PCR Master Mix (TaqMan, ROX) |
Cat. No. | TQ1100 | TQ1110 | TQ1200 | TQ1210 | TQ2110 |
Detection chemistry | SYBR | SYBR | SYBR | SYBR | TaqMan |
Blue contrast dye for best convenience | ü | ü | ü | ü | X |
ROX dye for reference | X | ü | X | ü | ü |
Time required for enzyme activation | 10 min | 10 min | 2 min | 2 min | 10 min |
qPCR program | Standard | Standard | Fast and Standard | Fast and Standard | Standard |
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还有你所用的荧光物质也有关系，Cy5以上应该可以活体成像。只看药物器官分布的话LZ可以用普通的小白鼠
然后剖腹观察，染料用Cy3或者其他普遍的FITC都行。
活体荧光成像一般有三种标记方法：荧光蛋白标记、荧光染料标记以及量子点标记。荧光蛋白适用于标记肿瘤细胞、病毒、基因等。通常使用GFP/EGFP/RFP等。荧光染料常用Cy3,Cy5以及Cy7。可以标记抗体、多肽、小分子药物。量子点标记是一种新的标记方法，楼主可自行查询
如果有，具体在哪个学校/单位/企业？
最近实验需要用到此设备。
如能告诉，不胜感谢！！！谢谢！！！
不知道哪家单位会有啊？
最近的实验会用到，哪位知道，请不吝赐教，越详细越好，多谢多谢！
丙酮法属于溶液法，是以有机溶剂稀释或溶解聚氨酯（或预聚体），再进行乳化的方法。在溶剂存在下，预聚体与亲水性扩链剂进行扩链反应，生成较高分子量的聚氨酯，反应过程可根据需要加人溶剂以降低聚氨酯溶液粘度，使之易于搅拌，然后加水进行分散，形成乳液，最后蒸去溶剂。溶剂以丙酮、甲乙酮居多，故称为丙酮法。此法的优点是丙酮、甲乙酮的沸点低、与水互容、易于回收处理，整个体系均匀，操作方便，由于降低粘度同时也降低了浓度，有利于在乳化之前制得高分子量的预聚体或聚氨酯树脂，所得乳液的膜性能比单纯预聚体法的好。而预聚体法由于粘度的限制，为了便于剪切分散，预聚体的分子量不能太高，可能会影响水性聚氨酯性能，例如粘度高则乳化困难，粒径大，乳液稳定性差；预聚体分子量小则NCO基团含量高，乳化后形成的脲键多，胶膜硬，缺乏柔软性。
Luciferase
）
标记细胞或
DNA
，而荧光技术则采用绿色荧光蛋白、红色荧光蛋白等荧光报告基因和
FITC
、
Cy5
、
C
y7
等荧光素及量子点
(quantumdot
，
QD)
进行标记。
小动物活体成像技术是采用高灵敏度制冷
CCD
配合特制的成像暗箱和图像处理，使得可以直接监
控活体生物体内的细胞活动和基因行为。实验者借此可以观测活体动物体内肿瘤的生长及转移、
感染性
疾病发展过程、特定基因的表达等生物学过程。
由于具有更高量子效率
CCD
的问世，使活体动物体内光学成像技术具有越来越高的灵敏度，对肿瘤微
小转移灶的检测灵敏度极高；另外，该技术不涉及放射性物质和方法，非常安全。因其操作极其简单、
所得结果直观、
灵敏度高、
实验成本低等特点，
在刚刚发展起来的几年时间内，
已广泛应用于生命科学、
医学研究及物开发等方面
（1）普通凝胶成像分析系统：可以对蛋白电泳凝胶，DNA凝胶样品进行图象采集并进行定性和定量分析，样品包括：EB、SYBR Green、SYBR Gold、Texas Red、GelStar、Fluoroscecin、 Radiant Red等染色的核酸监测；以及Coomassie Blue、SYPRO Orange、各种染色的蛋白质凝胶如考染等。（或UV,EB和有色及可见样品成像）；（2）化学发光成像分析系统：成像范围涵盖UV,EB,化学发光、紫外-荧光、有色及可见样品成像；（3）多色荧光成像分析系统：成像范围涵盖UV,EB,化学发光、多色荧光荧光、有色及可见样品成像；（4）多功能活体成像分析系统：UV,EB,化学发光、多色荧光荧光、有色及可见样品成像和离体组织和小型动物，及大型型动物。
我知道所以你知道！
