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货号 单位规格
目录价格 (CNY) 数量 11146-016 100 reactions
9,910.00 11146-024 25 reactions
2,919.00
产品概述
描述
ThermoScript™ Reverse Transcriptase (RT) 是鸟类 RT,RNase H 活性降低,设计用于具有高级结构,处理难度大的 RNA 模板的 RT-PCR。 ThermoScript™ RT-PCR 系统设计用于复制具有二级结构的 RNA 并改善引发的特异性。 与 PCR 结合使用时,该系统可用于检测稀有信使或者对来自少量细胞的特异性 mRNA 进行定量。 该系统含有 ThermoScript™ RT,克隆的鸟类反转录酶,这种酶经过改造,具有降低的 RNase H 活性和很高的热稳定性(最高 70°C)。 每个系统针对从总 RNA 或多聚 (A)+ RNA 产生第一链 cDNA 进行了优化 (1)(图 1)。 ThermoScript™ RT-PCR 系统:
• 针对 RT-PCR 进行了优化
• 可用于具有高级结构的 RNA 或基因特异性引物
• RNase H 活性降低,第一链 cDNA 产量更高
• 直接扩增第一链 cDNA 产物,无需有机萃取或沉淀
• 包含寡 (dT) 和随机六核苷酸以引发 cDNA 合成,用途灵活
• 可选择 Platinum® Taq DNA 聚合酶,在扩增最长达 3 kb 的模板时提供更高的特异性 (2)(图 2),或者 Platinum® Taq DNA 高保真聚合酶 (Platinum® Taq DNA Polymerase High Fidelity),以扩增最长达 12 kb 的模板(图 3)规格
Reverse Transcriptase: ThermoScript™ Downstream Application: Reverse Transcriptase PCR (RT-PCR) Reaction Format: Separate Components Primer Type: Oligo dT Primers, Random Primers Product Size: 25 reactions Shipping Condition: Dry Ice Optimal Reaction Temperature: 50-65°C 内容及储存
ThermoScript™ RT-PCR Systems are supplied with the components listed in Table 1. Store at -70°C. Guaranteed stable for 6 months when properly stored.手册
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手册和实验方案
化学品安全技术说明书(MSDS)
引用及参考文献
Rawat VP, Cusan M, Deshpande A, Hiddemann W, Quintanilla-Martinez L, Humphries RK, Bohlander SK, Feuring-Buske M, Buske C,
Proc Natl Acad Sci U S A (2004) 101:817-822
Product usage: First-strand cDNA was synthesized from 1 µg of total RNA by using the ThermoScript RT-PCR system. A PCR product was cloned in frame to the 3' end of the histidine epitope of pCDNA6/ His A plasmid.Liao P; Georgakopoulos D; Kovacs A; Zheng M; Lerner D; Pu H; Saffitz J; Chien K; Xiao R P; Kass D A; Wang Y;
Proc Natl Acad Sci U S A (2001) 98:12283-12291
Product usage: RNA samples were prepared from the heart tissues by using Trizol reagent (Life Technologies, Rockville, MD) according to the manufacturer's recommended protocol. The RNA dot-blot analysis was performed based on a published protocol using a set of oligonucleotide probes. Reverse tHolt Jeffrey R; Gillespie Susan K H; Provance D William; Shah Kavita; Shokat Kevan M; Corey David P; Mercer John A; Gillespie Peter G;
Cell (2002) 108:371-452
Product usage: We purified total RNA from utricles of genotyped mice, synthesized cDNA using oligo(dT)-containing primers, and carried out PCR (ThermoScript RT-PCR, Gibco-BRL).




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