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聚合酶链反应:从固定组织中扩增DNA

Polymerase chain reaction: amplification of DNA from fixed tissue.

作者信息

Crisan D, Cadoff E M, Mattson J C, Hartle K A

机构信息

Department of Pathology, University of Pittsburgh, PA 15213-2582.

出版信息

Clin Biochem. 1990 Dec;23(6):489-95. doi: 10.1016/0009-9120(90)80037-j.

Abstract

The polymerase chain reaction (PCR) allows the analysis of DNA from biologic samples containing only nanogram quantities of DNA. We used DNA purified from fresh or frozen peripheral blood (PB) leukocytes and formalin, or B-5 fixed bone marrow aspirate clots (BM). A sequence of the beta-globin gene was amplified via the PCR then hybridized with allele specific oligonucleotide probes for hemoglobin A, S, and C. All DNA preparations, including formalin and B-5 fixed BMs, were successfully amplified; the hybridization of the amplified products resulted in patterns consistent with the hemoglobin phenotype for all patients. PCR can be used on DNA from many sources; retrospective studies using paraffin embedded fixed tissue are possible because extremely small amounts of DNA present in fixed tissue can be successfully amplified.

摘要

聚合酶链反应(PCR)可用于分析仅含有纳克量DNA的生物样本中的DNA。我们使用从新鲜或冷冻外周血(PB)白细胞以及福尔马林或B-5固定的骨髓抽吸凝块(BM)中纯化的DNA。通过PCR扩增β-珠蛋白基因序列,然后与血红蛋白A、S和C的等位基因特异性寡核苷酸探针杂交。所有DNA制剂,包括福尔马林和B-5固定的骨髓,均成功扩增;扩增产物的杂交产生了与所有患者血红蛋白表型一致的模式。PCR可用于多种来源的DNA;使用石蜡包埋固定组织的回顾性研究是可行的,因为固定组织中存在的极少量DNA可以成功扩增。

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