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Protocol for purification of cells in their native state using reversible aptamer-antidote pairs.
Requena, Martin D; Gray, Bethany Powell; Sullenger, Bruce A.
Afiliação
  • Requena MD; Department of Surgery, Duke University Medical Center, 2 Genome Ct, Durham, NC 27710, USA; University Program in Genetics and Genomics, Duke University Medical Center, 2 Genome Ct, Durham, NC 27710, USA. Electronic address: mdr45@duke.edu.
  • Gray BP; Department of Surgery, Duke University Medical Center, 2 Genome Ct, Durham, NC 27710, USA; Department of Pharmacology and Molecular Sciences, The Johns Hopkins University School of Medicine, 725 North Wolfe St, Baltimore, MD 21205, USA.
  • Sullenger BA; Department of Surgery, Duke University Medical Center, 2 Genome Ct, Durham, NC 27710, USA; University Program in Genetics and Genomics, Duke University Medical Center, 2 Genome Ct, Durham, NC 27710, USA. Electronic address: bruce.sullenger@duke.edu.
STAR Protoc ; 4(3): 102348, 2023 Sep 15.
Article em En | MEDLINE | ID: mdl-37314924
ABSTRACT
Cell isolation from complex mixtures is a key step in many clinical and research applications, but standard isolation methods may affect the cell's biology and are difficult to reverse. Here, we present a method to isolate and restore cells to their native state using an aptamer that binds epidermal growth factor receptor (EGFR+)cells and a complementary antisense oligonucleotide to reverse binding. For complete details on the use and execution of this protocol, please refer to Gray et al.1.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oligonucleotídeos / Antídotos Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oligonucleotídeos / Antídotos Idioma: En Ano de publicação: 2023 Tipo de documento: Article