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Annealing and purification of fluorescently labeled DNA substrates for in vitro assays

We present a protocol to generate high-quality fluorescently labeled DNA substrates that can be used for biochemical assays, including DNA-binding and nuclease activity assays. We describe polyacrylamide-gel-electrophoresis-based purification of DNA oligonucleotides, followed by annealing the oligon...

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Detalles Bibliográficos
Autores principales: Tse, Ying Wah Elizabeth, Yun, Hwa Young, Wyatt, Haley Doris Myskiw
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9958487/
https://www.ncbi.nlm.nih.gov/pubmed/36853679
http://dx.doi.org/10.1016/j.xpro.2023.102128
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author Tse, Ying Wah Elizabeth
Yun, Hwa Young
Wyatt, Haley Doris Myskiw
author_facet Tse, Ying Wah Elizabeth
Yun, Hwa Young
Wyatt, Haley Doris Myskiw
author_sort Tse, Ying Wah Elizabeth
collection PubMed
description We present a protocol to generate high-quality fluorescently labeled DNA substrates that can be used for biochemical assays, including DNA-binding and nuclease activity assays. We describe polyacrylamide-gel-electrophoresis-based purification of DNA oligonucleotides, followed by annealing the oligonucleotides and purifying the annealed substrates using anion-exchange chromatography. This protocol circumvents the use of radioisotopes, which require training and dedicated equipment for safe handling and necessitate specialized waste disposal. This protocol is amenable to varying lengths of oligonucleotides and DNA substrates. For complete details on the use and execution of this protocol, please refer to Payliss and Tse et al. (2022).(1)
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spelling pubmed-99584872023-02-26 Annealing and purification of fluorescently labeled DNA substrates for in vitro assays Tse, Ying Wah Elizabeth Yun, Hwa Young Wyatt, Haley Doris Myskiw STAR Protoc Protocol We present a protocol to generate high-quality fluorescently labeled DNA substrates that can be used for biochemical assays, including DNA-binding and nuclease activity assays. We describe polyacrylamide-gel-electrophoresis-based purification of DNA oligonucleotides, followed by annealing the oligonucleotides and purifying the annealed substrates using anion-exchange chromatography. This protocol circumvents the use of radioisotopes, which require training and dedicated equipment for safe handling and necessitate specialized waste disposal. This protocol is amenable to varying lengths of oligonucleotides and DNA substrates. For complete details on the use and execution of this protocol, please refer to Payliss and Tse et al. (2022).(1) Elsevier 2023-02-20 /pmc/articles/PMC9958487/ /pubmed/36853679 http://dx.doi.org/10.1016/j.xpro.2023.102128 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Tse, Ying Wah Elizabeth
Yun, Hwa Young
Wyatt, Haley Doris Myskiw
Annealing and purification of fluorescently labeled DNA substrates for in vitro assays
title Annealing and purification of fluorescently labeled DNA substrates for in vitro assays
title_full Annealing and purification of fluorescently labeled DNA substrates for in vitro assays
title_fullStr Annealing and purification of fluorescently labeled DNA substrates for in vitro assays
title_full_unstemmed Annealing and purification of fluorescently labeled DNA substrates for in vitro assays
title_short Annealing and purification of fluorescently labeled DNA substrates for in vitro assays
title_sort annealing and purification of fluorescently labeled dna substrates for in vitro assays
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9958487/
https://www.ncbi.nlm.nih.gov/pubmed/36853679
http://dx.doi.org/10.1016/j.xpro.2023.102128
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