- ¥3452.90
- AIB/LIFE
- 美国
- A25918
- 2025年07月15日
相关产品推荐更多 >
万千商家帮你免费找货
0 人在求购买到急需产品
- 详细信息
- 文献和实验
- 技术资料
- 规格：
10 x 1 mL
PowerUp™ SYBR® Green Master Mix features include:
• A dual hot-start mechanism for excellent specificity
• Highly reproducible CTs over a broad dynamic range
• Inclusion of UDG to help prevent carryover contamination
• Stability of pre-assembled reactions for up to 72 hours
• Compatibility with most real-time qPCR instruments
Exceptional specificity with dual hot-start mechanism
Specificity is paramount in obtaining high-quality data in SYBR® Green reactions and can be enhanced through control of the Taq DNA polymerase at lower temperatures before stringent primer binding. PowerUp™ SYBR® Green Master Mix uses the Dual-Lock™ Taq DNA polymerase enzyme that combines two unique hot-start mechanisms to help control its activity and to prevent undesirable early activity of the polymerase at low temperatures. In an experiment evaluating 24 different primer sets, PowerUp™ SYBR® Green Master Mix generated single melt curves 100% of the time, consistent with highly specific amplification.
Tight reproducibility in CTs over a wide dynamic range
PowerUp™ SYBR® Green Master Mix demonstrates excellent reproducibility over a wide dynamic range for a variety of targets tested (see figure). In addition, this master mix provides efficient amplification over 6 logs of sample input. Unlike competitor mixes that can exhibit inhibition at high cDNA inputs and low correlation coefficients over a dynamic range experiment, PowerUp™ SYBR® Green Master Mix efficiency is maintained over the full dynamic range to help deliver maximal confidence in data quality (see figure).
UDG included for carryover contamination control
The inclusion of uracil-DNA glycosylase (UDG) and dUTP in the PowerUp™ SYBR® Green Master Mix enables the degradation of any previously amplified PCR products, helping prevent contamination of subsequent qPCR reactions and possible false positives.
Stability of pre-assembled reactions
The tight control of the Dual-Lock™ Taq DNA polymerase in PowerUp™ SYBR® Green Master Mix enables reactions to be assembled up to 72 hours prior to cycling without impacting data (see figure). This consistency allows users to have confidence and flexibility in the use of PowerUP™ SYBR® Green Master Mix across numerous workflow scenarios1.
Broad instrument compatibility
PowerUp™ SYBR® Green Master Mix can be used in either standard or fast cycling mode and is compatible with all Applied Biosystems® real-time PCR instruments2. It is also compatible with the Bio-Rad IQ™5 and CFX96™ / CFX384™ systems, Roche LightCycler® LC480, and Stratagene® MX3005P® systems. For optimal results, recommended primer concentrations are 300–800 nM.
风险提示：丁香通仅作为第三方平台，为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全，合理判断，谨慎选购商品，商家和用户对交易行为负责。对于医疗器械类产品，请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验用ReadyMixTM PCR Reaction Mix进行拟南芥SSLP
。 100 bp DNA Ladder可确定100-1500 bp长的双链DNA。 1、首先称量3 g琼脂糖，然后加120 ml 0.5×TBE缓冲液，称量其重量。 2、用微波炉加热融化，直至看不到琼脂糖颗粒，然后再称重，加水至原加热前重量。 3、用胶布构建倒胶槽，在融化的琼脂糖溶液中加5 µl SYBR SAFETM DNA gel stain，混匀。 4、待琼脂糖冷至60℃后，倒入制胶槽，让其在室温下冷却。 5、除去胶布，将制胶槽放入电泳槽，加0.5×TBE
(BD Biosciences / Clontech). SYBR Green PCR master mix, 200 reactions (Applied Biosystems). Optical tube and cap strips (Applied Biosystems). SuperScript
ChamQTM/AceQ® QPCR Master Mix 5 ml 可供 20 μl 体系 500 次反应。 模板的上样量 若直接使用 cDNA 原液作为模板，建议使用体积不超过 qPCR 反应总体积的 1 / 10！ 当复孔之间重复性不佳时，可将模板做适当稀释后以大体积加入反应体系，可有效提高实验重复性。看小 V 做的实验，是不是重复性爆表啊～～～ 预变性时间 常见的 qPCR 试剂预变性时间从 30 sec - 15 min 不等。科学家们为了封闭常温下酶的活性，使 qPCR 产生
技术资料暂无技术资料 索取技术资料
