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  Protocol for chromatin accessibility profiling of human endothelial cells cultured under fluid shear stress using ATAC-seq

Raaz, L., Mendez, P.-L., Mundlos, S., Knaus, P., & Jatzlau, J. (2024). Protocol for chromatin accessibility profiling of human endothelial cells cultured under fluid shear stress using ATAC-seq. STAR Protocols, 5(1): 102859. doi:10.1016/j.xpro.2024.102859.

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STAR Protocols_Raaz et al_2024.pdf (Publisher version), 6MB
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STAR Protocols_Raaz et al_2024.pdf
Description:
Protocol
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Gold
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application/pdf / [MD5]
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© 2024

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 Creators:
Raaz, Lion1, Author                 
Mendez, Paul-Lennard2, Author                 
Mundlos, Stefan1, Author                 
Knaus, Petra, Author
Jatzlau, Jerome1, Author
Affiliations:
1Research Group Development & Disease (Head: Stefan Mundlos), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1433557              
2IMPRS for Biology and Computation (Anne-Dominique Gindrat), Dept. of Computational Molecular Biology (Head: Martin Vingron), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1479666              

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Free keywords: Cell Biology; Genomics; Molecular Biology
 Abstract: Chromatin accessibility influences gene regulation and can be quantified using assay for transposase-accessible chromatin with high-throughput sequencing (ATAC-seq). Recapitulating in vivo fluid shear stress (FSS) mechano-regimes in vitro allows the study of atheroprone and atheroprotective mechanisms. In this protocol, we show how to culture and harvest endothelial cells from microfluidic channels for the preparation of ATAC-seq, highlighting optional growth factor stimulation and different FSS rates. This extends the application of ATAC-seq to the analysis of in vitro mechanically stimulated cells.

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Language(s): eng - English
 Dates: 2024-02-072024-03-15
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: DOI: 10.1016/j.xpro.2024.102859
PMID: 38329877
PMC: PMC10865476
 Degree: -

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Title: STAR Protocols
Source Genre: Journal
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Publ. Info: Cambridge, MA ; Amsterdam : Cell Press ; Elsevier
Pages: - Volume / Issue: 5 (1) Sequence Number: 102859 Start / End Page: - Identifier: ISSN: 2666-1667
CoNE: https://pure.mpg.de/cone/journals/resource/2666-1667