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Drosophila melanogaster strain:Kc167

ABSTRACT: Drosophila Kc167 and S2 Mcm2-7 ChIP-seq in HU

PROVIDER: PRJNA268524 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR1663771.fastq.gz	Fastqsanger.gz
	SRR1663315.fastq.gz	Fastqsanger.gz
	SRR1663917.fastq.gz	Fastqsanger.gz
	SRR1663918.fastq.gz	Fastqsanger.gz

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Kc167 Mcm2-7 Localization in HU

Project description:Determination of the genome-wide distribution of the Mcm2-7 helicase by chromatin immunoprecipitation in the Drosophila Kc167 cell line at the beginning of S phase. Kc167 cells were arrested at the G1/S transition with hydroxyurea (HU). Goal was to evaluate changes in the genome-wide Mcm2-7 distribution throughout the cell cycle, and how this relates to the excess Mcm2-7 loaded onto chromatin in G1. ChIP-Chip of Mcm2-7 in HU compared to input genomic DNA. Biological Replicates: 2

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Kc167 Mcm2-7 Localization in Late S Phase

Project description:Determination of the genome-wide distribution of the Mcm2-7 helicase by chromatin immunoprecipitation in the Drosophila Kc167 cell line at the end of S phase. Kc167 cells were synchronized by first arresting at the G1/S transition with hydroxyurea (HU), and then releasing from the HU arrest point for 6 hours. Goal was to evaluate changes in the genome-wide Mcm2-7 distribution throughout the cell cycle, and how this relates to the excess Mcm2-7 loaded onto chromatin in G1.

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Kc167 ORC Localization in hydroxyurea (HU)

Project description:Determination of the genome-wide distribution of ORC by chromatin immunoprecipitation in the Drosophila Kc167 cell line at the beginning of S phase. Kc167 cells were arrested at the G1/S transition with hydroxyurea (HU). Goal was to test whether the ORC binding distribution remained the same between G1 and S. ChIP-Chip of ORC in HU compared to input genomic DNA. Biological Replicates: 1

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