
Product Highlights
- Reproducible – consistent results between technical replicates for increased confidence in results
- Specific – antibody-mediated hot-start DNA polymerase minimizes non-specific amplification for improved assay sensitivity and reliability
- Sensitive – reliable quantification of low abundance targets and scarce samples
- Robust – reliable, accurate detection of DNA and RNA targets from a broad range of sample types
- Fast – delivers reproducible, accurate assay results in as little as 30 minutes
Product Description
The SensiFAST™ SYBR & Fluorescein Kit has been developed for fast, highly accurate real-time PCR and has been validated on real-time PCR platforms that require the passive reference dye fluorescein for collection of dynamic well factors.
A combination of the latest advances in buffer chemistry and PCR enhancers ensures that the SensiFAST SYBR & Fluorescein Kit produces reliable assay results under fast thermal cycling conditions. An antibody-mediated hot-start DNA polymerase system promotes highly-specific amplification, in turn improving assay sensitivity and dynamic range.
The SensiFAST SYBR & Fluorescein Kit has been optimized to deliver optimal performance in tandem with the SensiFAST cDNA Synthesis Kit, which offers fast, unbiased cDNA synthesis, without compromising cDNA yield or coverage.
Applications
- Gene expression analysis
- DNA / RNA target detection
- miRNA profiling / quantification
- Copy number variation (CNV) analysis

SensiFAST Products Customer Review
SensiFAST SYBR No-ROX One-Step Kit Customer Review
Real-Time PCR Selection Chart
One-step Vs. Two-step real-time RT PCR
A discussion of the pros and cons of each detection strategy.ebiomall.com






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2.SNaPshot法 该技术由美国应用生物公司(ABI)开发,是基于荧光标记单碱基延伸原理的分型技术,也称小测序,主要针对中等通量的SNP分型项目。在一个含有测序酶、四种荧光标记ddNTP、紧临多态位点5’-端的不同长度延伸引物和PCR产物模板的反应体系中,引物延伸一个碱基即终止,经ABI测序仪检测后,根据峰的移动位置确定该延伸产物对应的SNP位点,根据峰的颜色可得知掺入的碱基种类,从而确定该样本的基因型。对于PCR产物模板可通过多重PCR反应体系来获得。通常用于10-30个SNP位点分析。
用takara的in-fusion方法做了个重组质粒,如左图PCR验证,右起第二道是空载质粒为模板的对照。右图是酶切验证,两个图片结合起来觉得除了第四个单克隆外,其他几个应该都可能是阳性克隆。结果送了1,2两个样品后测序的结果都不对。为什么会这样。
期待着高手们的指点,谢谢。
不是很相信网上的商家,遂求助各位路过的大虾们,有用过的吗?这些酶特异性怎样啊?贵不贵,跟我直接测序相比,有优势吗?
●应用酶水解多肽不会破坏氨基酸,也不会发生消旋化。水解的产物为较小的肽段。向左转|向右转
请教高人,这样的问题怎么解决?
多谢
目的片段用kpn1和xho1双酶切,然后连接到PGL4.10上,结果用RPV3测序出来目的序列是反向互补的,这是什么原因导致的?
利用NheI和HindIII双酶切插入目的片段,为什么双酶切有目的片段和切开的质粒,测序却没有?
并且测序后在NheI位点后的序列变成了-GGCTAGGTAC-Kpn位点(CGTTTAAACTTAAGCTTG消失。之前和之后的序列都相符),之间的怎么都没了?

