ChIP-Seq from Limited Starting Material of K562 Cells and

Easy workflow High Signal-to-Noise ratio High reproducibility Low Input ChIP-Seq Tagmentation

Journal

Bio-protocol
ISSN: 2331-8325
Titre abrégé: Bio Protoc
Pays: United States
ID NLM: 101635102

Informations de publication

Date de publication:
20 Feb 2020
Historique:
received: 15 08 2019
revised: 16 12 2019
accepted: 23 12 2019
entrez: 3 3 2021
pubmed: 4 3 2021
medline: 4 3 2021
Statut: epublish

Résumé

Chromatin immunoprecipitation is extensively used to investigate the epigenetic profile and transcription factor binding sites in the genome. However, when the starting material is limited, the conventional ChIP-Seq approach cannot be implemented. This protocol describes a method that can be used to generate the chromatin profiles from as low as 100 human or 1,000

Identifiants

pubmed: 33654745
doi: 10.21769/BioProtoc.3520
pii: e3520
pmc: PMC7842548
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e3520

Informations de copyright

Copyright 2020 The Authors; exclusive licensee Bio-protocol LLC.

Déclaration de conflit d'intérêts

Competing interestsThe authors declare no financial and non-financial competing interest.

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Auteurs

Junaid Akhtar (J)

Institute of Developmental Biology and Neurobiology, University of Mainz, Hanns-Dieter-Hsch Weg 15, 55128 Mainz, Germany.

Piyush More (P)

Department of Pharmacology, University Medical Center, Johannes Gutenberg University of Mainz, 55131 Mainz, Germany.

Steffen Albrecht (S)

Faculty of Biology, Johannes Gutenberg University Mainz, Hans-Dieter-Hsch-Weg 15, 55128, Mainz, Germany.

Classifications MeSH