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首页> 外文期刊>Nucleic acids research >Telomeric repeat amplification, without shortening or lengthening of the telomerase products: a method to analyze the processivity of telomerase enzyme
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Telomeric repeat amplification, without shortening or lengthening of the telomerase products: a method to analyze the processivity of telomerase enzyme

机译:端粒重复扩增,而不会缩短或延长端粒酶产物:一种分析端粒酶合成能力的方法

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摘要

The Telomeric Repeat Amplification Protocol (TRAP) and its modified versions (including ours, TP-TRAP) change the size and/or the ratio of the telomerase products in the amplification stage of the assay. Based on our recently published method we developed a new TRAP. This method ensures that the number of telomeric repeats present in the original telomerase products does not change on PCR amplification. The usefulness of the method was proved with amplification of chemically synthesized telomerase products and a newly designed telomerase substrate oligonucleotide. This is the first report in which the PCR products directly reflect the size distribution of telomerase products generated by the enzyme.
机译:端粒重复扩增协议(TRAP)及其修改版本(包括我们的TP-TRAP)在测定的扩增阶段会改变端粒酶产物的大小和/或比例。基于我们最近发布的方法,我们开发了一种新的TRAP。该方法确保了原始端粒酶产物中存在的端粒重复序列的数量在PCR扩增时不会改变。通过化学合成的端粒酶产物的扩增和新设计的端粒酶底物寡核苷酸证明了该方法的有效性。这是第一份报告,其中PCR产物直接反映了由酶产生的端粒酶产物的大小分布。

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