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dNTP Mixture

dNTP混合物

Company: Takara Bio
Catalog#: 4030
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CRISPR-PCS Protocol for Chromosome Splitting and Splitting Event Detection in Saccharomyces cerevisiae
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Date:
2017-05-20
[Abstract]  Chromosome engineering is an important technology with applications in basic biology and biotechnology. Chromosome splitting technology called PCS (PCR-mediated Chromosome Splitting) has already been developed as a fundamental chromosome engineering technology in the budding yeast. However, the splitting efficiency of PCS technology is not high enough to achieve multiple splitting at a time. This protocol describes a procedure for achieving simultaneous and multiple chromosome splits in the budding yeast Saccharomyces cerevisiae by a new technology called CRISPR-PCS. At least four independent sites in the genome can be split by one transformation. Total time and labor for obtaining a multiple split yeast strain is drastically reduced when compared with conventional PCS ... [摘要]  染色体工程是应用于基础生物学和生物技术的重要技术。染色体分裂技术称为PCS(PCR介导的染色体分裂)已经被开发为发芽酵母中的基本染色体工程技术。然而,PCS技术的分割效率不够高,不能一次实现多次分割。该协议描述了通过称为CRISPR-PCS的新技术在芽状酵母酿酒酵母中实现同时和多个染色体分裂的过程。基因组中至少四个独立的位点可以通过一次转化来分裂。与常规PCS技术相比,获得多重分裂酵母菌株的总时间和劳动力大大降低。

背景 能够快速有效地操纵多个遗传基因座或染色体区域的染色体工程技术变得越来越重要。这些技术为阐明染色体和基因组功能提供了有力的手段。此外,它可以用于通过创建广泛的遗传变体来繁殖有用的菌株。在芽殖酵母酿酒酵母(Saccharomyces ...

Determination of the Secondary Structure of an RNA fragment in Solution: Selective 2`-Hydroxyl Acylation Analyzed by Primer Extension Assay (SHAPE)
Author:
Date:
2015-01-20
[Abstract]  This protocol describes the methodology for the determination of the secondary structure of an RNA fragment in solution using Selective 2´-Hydroxyl Acylation analyzed by Primer Extension, abbreviation SHAPE. It consists in the very fast chemical modification of flexible and therefore possibly single-stranded nucleotides in a sequence-independent manner using benzoyl cyanide (BzCN), forming 2´-O-adducts. The modifications in the RNA are then analyzed by primer extension. Reverse transcriptase is blocked by the 2´-O-adducts formed. The advantage of the method is, first, that not each RNA molecule studied but the primer used in the extension reaction is labelled and, second, that the resulting cDNA analyzed in sequencing gels is much more stable than the modified RNA. [摘要]  该方案描述了使用通过引物延伸(缩写为SHAPE)分析的选择性2'-羟基酰化来确定溶液中RNA片段的二级结构的方法。 其包括使用苯甲酰氰(BzCN)以序列非依赖性方式非常快速地化学修饰柔性且因此可能的单链核苷酸,形成2'-O-加合物。 然后通过引物延伸分析RNA中的修饰。 逆转录酶被形成的2'-O-加合物阻断。 该方法的优点是,首先,不是每个RNA分子研究,而是在延伸反应中使用的引物被标记,其次,在测序凝胶中分析得到的cDNA比修饰的RNA更稳定。

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