Protocol for the simultaneous isolation of DNA, RNA, and miRNA from a single archived Kaposi sarcoma biopsy.

IF 1.3 Q4 BIOCHEMICAL RESEARCH METHODS STAR Protocols Pub Date : 2024-12-20 Epub Date: 2024-10-04 DOI:10.1016/j.xpro.2024.103365
Larissa L S Scholte, Justin Browne, David J Nolan, Peyton St John, Katherine Tracy, Rafaela S Thur, Ghangzhao Li, Susanna L Lamers, Paige Bracci, Michael S McGrath, Jeffrey M Bethony
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引用次数: 0

Abstract

Kaposi sarcoma (KS) punch biopsies present unique challenges for extracting nucleic acids, which can be exacerbated by their long-term stabilization in RNAlater. Here, we present a protocol for simultaneously isolating DNA, RNA, and miRNA from a single KS punch biopsy. We detail the steps for preparing reagents and supplies, disrupting KS tissue using manual and mechanical methods, isolating DNA and total RNA, evaluating nucleic acid quality, and storing nucleic acids long-term.

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从单个存档卡波西肉瘤活检组织中同时分离 DNA、RNA 和 miRNA 的方案。
卡波西肉瘤(KS)打孔活检为提取核酸带来了独特的挑战,而核酸在 RNAlater 中的长期稳定又加剧了这种挑战。在此,我们介绍一种同时从单个 KS 穿孔活检组织中分离 DNA、RNA 和 miRNA 的方案。我们详细介绍了准备试剂和用品、使用手工和机械方法破坏 KS 组织、分离 DNA 和总 RNA、评估核酸质量以及长期储存核酸的步骤。
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来源期刊
STAR Protocols
STAR Protocols Biochemistry, Genetics and Molecular Biology-General Biochemistry, Genetics and Molecular Biology
CiteScore
2.00
自引率
0.00%
发文量
789
审稿时长
10 weeks
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