|
Status |
Public on Oct 15, 2013 |
Title |
Pu1 FDCPmix E [ChIP-seq] |
Sample type |
SRA |
|
|
Source name |
FDCPmix
|
Organism |
Mus musculus |
Characteristics |
cell line: FDCPmix Stage: 5 days erythroid differentiation chip antibody: Pu1 chip antibody vendor: santa cruz biotechnology chip antibody cat.#: sc352x
|
Treatment protocol |
For differentiation, cells were washed and then triplicate samples were cultured in IMDM plus 10% FCS and low IL-3 supplemented with either Epo and hemin (erythroid output) or G-CSF and SCF (neutrophil output). GATA1ERT and Pu.1ERT were subcloned into the pHR-SIN-CSGWEmGFP lentiviral expression construct under control of the SFFV promoter. Gata2 and Pu.1 shRNAs were subcloned into Lentilox 3.7.
|
Growth protocol |
FDCPmix were routinely maintained in Fischer's medium. For differentiation cells were washed and cultured in IMDM plus 10% FCS and low IL-3 with either Epo+hemin (erythoid) or GCSF+SCF (myeloid)
|
Extracted molecule |
genomic DNA |
Extraction protocol |
FDCPmix cells were cross-linked with 1% formaldehyde and sonicated so that the bulk of the chromatin was between 100-500 bp. ChIP was essentially performed by standard procedures Libraries were made using the ChIP-Seq sample preparation kit (cat# IP-102-1001, Illumina, San Diego, CA, USA) as per manufacture’s instruction.
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina Genome Analyzer II |
|
|
Description |
Sample 6
|
Data processing |
Reads were mapped to the mm9 genome using bowtie (v0.12.3) Peaks were called against an IgG control with MACS (v1.3.7.1, mfold=15,bw=100) and Peakranger (v1.02, b=100,p=0.01,t=4) where a peak was called so if found by both algorithms within 90bp. Genome_build: mm9 Supplementary_files_format_and_content: peak files
|
|
|
Submission date |
Aug 28, 2013 |
Last update date |
May 15, 2019 |
Contact name |
Shamit Soneji |
E-mail(s) |
shamit.soneji@med.lu.se
|
Organization name |
BMC
|
Street address |
Sölvegatan 19
|
City |
Lund |
ZIP/Postal code |
221 84 |
Country |
Sweden |
|
|
Platform ID |
GPL9250 |
Series (2) |
GSE49991 |
Dynamic analysis of gene expression and genome wide transcription factor binding during lineage-specification of multipotent progenitors |
GSE50406 |
Dynamic analysis of gene expression and genome wide transcription factor binding during lineage-specification of multipotent progenitors [ChIP-seq]. |
|
Relations |
BioSample |
SAMN02338392 |
SRA |
SRX340958 |