
Description
Product Highlights
- Accurate – clear discrimination of even the most challenging sequence differences
- Reproducible – unparalleled consistency between replicate difference plots for increased confidence in sample characterization
- Sensitive – efficient detection from even very limiting amounts of sample
- Flexible – enables reliable characterization of a broad range of sequence differences
- Fast – rapid PCR amplification prior to high resolution melting, enabling higher throughput
Product Description
SensiFAST HRM Kit has been developed for detailed characterization of samples according to their base composition, length and GC content by high resolution melting. The latest advances in buffer chemistry and enhancers, together with an antibody-mediated hot-start DNA polymerase system, ensure the SensiFAST HRM Kit delivers reproducible, accurate HRM analysis.
SensiFAST HRM Kit contains EvaGreen®, a third generation, saturating fluorescent dye which selectively binds to double-stranded DNA. In contrast to dyes such as SYBR® Green I, EvaGreen can be used at higher concentrations without inhibiting PCR and shows equal binding affinity for GC-rich and AT-rich regions. The combination of our SensiFAST DNA Polymerase, unique buffer system and EvaGreen dye enables amplification and discrimination of even the most challenging sequence differences, such as class IV SNPs without sequence preference. Since it does not require expensive labelled oligonucleotide probes, SensiFAST HRM Kit is also a cost effective alternative to traditional probe based genotyping methods.
Applications
- SNP genotyping
- Characterization of haplotype blocks
- DNA mapping
- Detection of insertions, deletions and translocations
- DNA fingerprinting
- DNA methylation analysis
- Gene scanning
- Species identification
- Allelic prevalence population studies
- Screening for loss of heterozygosity

Introduction to SensiFAST
Overview, features and benefits of the SensiFAST product familyReal-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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没有序列识别的功能,他就是简单的催化相邻DNA链的5-P末端和3'-OH末端以磷酸二酯键结合的反应,需ATP作辅酶。 不仅可以催化粘性末端之间或平滑末端之间的DNA的连接,也催化DNA与RNA之间以及少数RNA之间的连接。
反转录酶(Reversetranscripatase)是以RNA为模板指导三磷酸脱氧核苷酸合成互补DNA(cDNA)的酶。哺乳类C型病毒的反转录酶和鼠类B型病毒的反转录酶都是一条多肽链。鸟类RNA病毒的反转录酶则由两上亚基结构。真核生物中也都分离出具有不同结构的反转录酶。
只要是细胞,就得走向衰老,现代研究表明,细胞的衰老和端粒的变短有关系。端粒就是DNA,随着细胞分裂次数的增多,端粒在不断变短,端粒酶就是组织端粒变短的。然而正常细胞中,端粒酶的活性受抑制,端粒酶是怎么染端粒变长的呢?实际上端粒酶是由RNA组成的,可以根据碱基互补配对逆转形成DNA,使得变短的端粒变长。所以说端粒酶可以逆转录形成端粒,使端粒不减短!
我在做5RACE,选用TaKaRa公司的RNA反转录酶(RNaseH-),不知道这个酶好不好,有什么需要注意的。

