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多色引物原位标记法和多色肽核酸

Multicolor PRINS and multicolor PNA.

作者信息

Pellestor F, Paulasova P, Andréo B, Lefort G, Hamamah S

机构信息

CNRS UPR 1142, Institute of Human Genetics, Montpellier, France.

出版信息

Cytogenet Genome Res. 2006;114(3-4):263-9. doi: 10.1159/000094211.

Abstract

Both PRimed IN Situ (PRINS) and Peptide Nucleic Acid (PNA) technologies have emerged as research techniques, but they have quickly evolved to applications in biological diagnosis assays. The two procedures now constitute efficient alternatives to the conventional fluorescence in situ hybridization (FISH) procedure for in situ chromosome identification and aneuploidy detection. They present several advantages (specificity, speed, discriminating ability) that make them very attractive for a number of cytogenetic purposes. Multicolor PRINS and PNA protocols have been described for the specific identification of human chromosomes. Various applications have already been developed in human genetics and new adaptations are ongoing.

摘要

引物原位标记(PRINS)技术和肽核酸(PNA)技术最初都是作为研究技术出现的,但它们很快就发展到可应用于生物诊断分析。目前,这两种方法已成为传统荧光原位杂交(FISH)方法的有效替代方法,用于原位染色体鉴定和非整倍体检测。它们具有多种优势(特异性、速度、鉴别能力),这使得它们在许多细胞遗传学应用中极具吸引力。已经有用于人类染色体特异性鉴定的多色PRINS和PNA方案。在人类遗传学领域已经开发了各种应用,并且新的应用正在不断涌现。

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