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聚合酶链反应-单链构象多态性分析:一种用于遗传疾病分子分析的方法。

PCR-SSCP: a method for the molecular analysis of genetic diseases.

作者信息

Kakavas V Konstantinos, Plageras Panagiotis, Vlachos T Antonios, Papaioannou Agelos, Noulas V Argiris

机构信息

Laboratory of Clinical Chemistry, School of Medical Laboratories, Faculty of Health and Care, Highest Technological Institute of Larissa, Greece.

出版信息

Mol Biotechnol. 2008 Feb;38(2):155-63. doi: 10.1007/s12033-007-9006-7. Epub 2007 Oct 13.

Abstract

Single strand conformation polymorphism (SSCP) is a reproducible, rapid and quite simple method for the detection of deletions/insertions/rearrangements in polymerase chain reaction amplified DNA. All the details for the use of PCR-SSCP are presented in the direction of genetic diseases (beta-thalassaemia, cystic fibrosis), optimum gel conditions, sensitivity and the latest modifications of the method, which are applied in most laboratories. This non-radioactive PCR-SSCP method can be reliably used to identify mutations in patients (beta-globin, CFTR), provided suitable controls are available. Moreover, it is widely used for mutation identification in carriers (beta-thalassaemia, cystic fibrosis), making it particularly useful in population screening.

摘要

单链构象多态性(SSCP)是一种用于检测聚合酶链反应扩增DNA中的缺失/插入/重排的可重复、快速且相当简单的方法。关于PCR-SSCP使用的所有细节都在遗传疾病(β地中海贫血、囊性纤维化)的方向、最佳凝胶条件、灵敏度以及该方法的最新改进方面进行了阐述,这些内容在大多数实验室中都有应用。这种非放射性的PCR-SSCP方法在有合适对照的情况下,可可靠地用于识别患者(β珠蛋白、CFTR)中的突变。此外,它还广泛用于携带者(β地中海贫血、囊性纤维化)的突变鉴定,使其在群体筛查中特别有用。

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