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原位聚合酶链反应:细胞内HIV-1前病毒DNA及其他特定基因的扩增与检测

Polymerase chain reaction in situ: intracellular amplification and detection of HIV-1 proviral DNA and other specific genes.

作者信息

Bagasra O, Seshamma T, Pomerantz R J

机构信息

Department of Medicine, Jefferson Medical College, Philadelphia, PA 19107.

出版信息

J Immunol Methods. 1993 Jan 14;158(1):131-45. doi: 10.1016/0022-1759(93)90265-9.

Abstract

The ability to detect a single copy of a specific gene in situ has many advantages and multiple applications in molecular biology, pathology and cell biology. We report here a unique, highly sensitive and specific technique which can be utilized to detect a single copy of human immunodeficiency virus type I (HIV-1) provirus and other genes, at the single cell level, by in situ amplification of a portion of a gene sequence. In this method, a polymerase chain reaction (PCR) can be carried out in situ, in fixed cells, on specially designed glass slides. After amplification one can detect the amplified signals by the in situ hybridization method, utilizing either biotinylated probes or 32P-labelled probes. The early molecular events in the retroviral life-cycle of HIV-1, in specific target cells, are demonstrated utilizing in situ PCR. The techniques utilized in this procedure and various potential uses of this methodology are described.

摘要

在原位检测特定基因单拷贝的能力在分子生物学、病理学和细胞生物学中具有诸多优势及多种应用。我们在此报告一种独特、高度灵敏且特异的技术,该技术可通过对基因序列的一部分进行原位扩增,在单细胞水平检测人类免疫缺陷病毒I型(HIV-1)前病毒及其他基因的单拷贝。在这种方法中,聚合酶链反应(PCR)可在固定细胞中于特制的载玻片上原位进行。扩增后,可利用生物素化探针或32P标记探针,通过原位杂交方法检测扩增信号。利用原位PCR展示了HIV-1在特定靶细胞中的逆转录病毒生命周期早期分子事件。描述了本实验过程中所使用的技术以及该方法的各种潜在用途。

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