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采用流式细胞术和荧光原位杂交技术来测量端粒的平均长度(流式荧光原位杂交技术)。

Flow cytometry and FISH to measure the average length of telomeres (flow FISH).

作者信息

Baerlocher Gabriela M, Vulto Irma, de Jong Gary, Lansdorp Peter M

机构信息

Terry Fox Laboratory, British Columbia Cancer Agency, 675 West 10th Avenue, Vancouver, British Columbia, V5Z 1L3, Canada.

出版信息

Nat Protoc. 2006;1(5):2365-76. doi: 10.1038/nprot.2006.263.

Abstract

Telomeres have emerged as crucial cellular elements in aging and various diseases including cancer. To measure the average length of telomere repeats in cells, we describe our protocols that use fluorescent in situ hybridization (FISH) with labeled peptide nucleic acid (PNA) probes specific for telomere repeats in combination with fluorescence measurements by flow cytometry (flow FISH). Flow FISH analysis can be performed using commercially available flow cytometers, and has the unique advantage over other methods for measuring telomere length of providing multi-parameter information on the length of telomere repeats in thousands of individual cells. The accuracy and reproducibility of the measurements is augmented by the automation of most pipetting (aspiration and dispensing) steps, and by including an internal standard (control cells) with a known telomere length in every tube. The basic protocol for the analysis of nucleated blood cells from 22 different individuals takes about 12 h spread over 2-3 days.

摘要

端粒已成为衰老及包括癌症在内的各种疾病中至关重要的细胞元件。为了测量细胞中端粒重复序列的平均长度,我们描述了我们的实验方案,该方案使用与端粒重复序列特异性结合的标记肽核酸(PNA)探针进行荧光原位杂交(FISH),并结合流式细胞术进行荧光测量(流式FISH)。流式FISH分析可使用市售的流式细胞仪进行,与其他测量端粒长度的方法相比,具有独特优势,能够提供数千个单个细胞中端粒重复序列长度的多参数信息。大多数移液(吸取和分配)步骤的自动化以及在每个试管中加入具有已知端粒长度的内标(对照细胞),提高了测量的准确性和可重复性。分析来自22个不同个体的有核血细胞的基本实验方案大约需要12小时,分2至3天完成。

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