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寡核苷酸 DNA 的纯化以提高杂交链反应性能。

Purification of DNA oligonucleotides to improve hybridization chain reaction performance.

机构信息

Department of Pharmaceutical Biosciences, Pharmaceutical Cell Biology, Uppsala University, Uppsala, Sweden.

出版信息

N Biotechnol. 2023 Sep 25;76:33-40. doi: 10.1016/j.nbt.2023.04.004. Epub 2023 Apr 12.

Abstract

Hybridization Chain Reaction (HCR) is a technique to generate a linear polymerization of oligonucleotide hairpins, used in multiple molecular biology methods. The HCR reaction is dependent on every hairpin being metastable in the absence of a triggering oligonucleotide and that every hairpin can continue the polymerization, which puts a strong demand on oligonucleotide quality. We show how further purification can greatly increase polymerization potential. It was found that a single extra PAGE-purification could greatly enhance hairpin polymerization both in solution and in situ. Purification using a ligation-based method further improved polymerization, yielding in situ immunoHCR stains at least 3.4-times stronger than a non-purified control. This demonstrates the importance of not only good sequence design of the oligonucleotide hairpins, but also the demand for high quality oligonucleotides to accomplish a potent and specific HCR.

摘要

杂交链式反应(HCR)是一种产生寡核苷酸发夹的线性聚合的技术,用于多种分子生物学方法。HCR 反应依赖于每个发夹在没有触发寡核苷酸的情况下处于亚稳态,并且每个发夹都可以继续聚合,这对寡核苷酸的质量提出了很高的要求。我们展示了进一步的纯化如何大大提高聚合潜力。结果发现,额外进行一次 PAGE 纯化可以大大提高溶液中和原位的发夹聚合。使用基于连接的方法进行纯化进一步提高了聚合作用,使得原位免疫 HCR 染色比未纯化的对照至少强 3.4 倍。这证明了不仅寡核苷酸发夹的良好序列设计很重要,而且还需要高质量的寡核苷酸才能实现有效的特异性 HCR。

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