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Status |
Public on Jan 24, 2018 |
Title |
Next Generation Sequencing based on the DNA fragment pulled down by p53 antibody (Santa Cruz, sc-126) from MCF7 wile type and MCF7 MDMX-C463A/WT cells. |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
Hypothesis: Based on gene chip results and further investigation, MDMX C463A/WT cells shows large portion of transcripts change at p53 dependent manner. As transcriptional factor, p53 regulates those genes could be related to DNA binding status change. ChIP-seq was used to test this hypothesis and figure out global map of p53 binding in MCF7 C463A/WT MCF7 cells by using MCF7 parental cells as reference.
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Overall design |
Examination of p53 genomic DNA binding affinity change in MCF7 C463A/WT cells comparing to parental cells.
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Contributor(s) |
Yuan Z, Zeng W |
Citation missing |
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Submission date |
Jan 23, 2018 |
Last update date |
Mar 27, 2019 |
Contact name |
Zhi-Min Yuan |
E-mail(s) |
zyuan@hsph.harvard.edu
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Phone |
6174322139
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Organization name |
Harvard University
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Department |
School of Public Health
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Lab |
John B. Little Center
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Street address |
Goldenson Building, Long wood Ave.
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City |
Boston |
State/province |
Massachusetts |
ZIP/Postal code |
02120 |
Country |
USA |
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Platforms (1) |
GPL11154 |
Illumina HiSeq 2000 (Homo sapiens) |
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Samples (4)
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This SubSeries is part of SuperSeries: |
GSE109482 |
Expression data and ChIP-seq from MCF7 wildtype and MCF7 MDMXC463A/WT cells |
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Relations |
BioProject |
PRJNA431182 |
SRA |
SRP131121 |