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Sample GSM545881 Query DataSets for GSM545881
Status Public on Jun 23, 2011
Title MEL_Input
Sample type SRA
 
Source name Murine erythroleukemia (MEL) cells stably transfected with Gata-1 fused to ER
Organism Mus musculus
Characteristics clone #: 4
chip antibody: N/A
Growth protocol MEL cells were grown in DMEM supplemented with 10% FBS (Gemini), 2mM L-glutamine, and 5mg/ml puromycin. ES-EPs were cultured in StemPro34 media (Invitrogen) supplmented with 2u/ml Epogen (Amgen), 40ng/ml hIGF-1 (Sigma), 10-6M dexamethosone (Sigma), 100ng/ml murine SCF (R&D Systems/Invitrogen), and 0.1% -mercaptoethanol (Gibco). ES-EP were maintained between 1-6x106 cells/ml by adding fresh media daily.
Extracted molecule genomic DNA
Extraction protocol Libraries were prepared as recommended by Illumina.
 
Library strategy ChIP-Seq
Library source genomic
Library selection ChIP
Instrument model Illumina Genome Analyzer II
 
Description Input DNA that was used for chromatin immunoprecipitation
Data processing Peak detection to mm9 was done using cisGenome and spp software.
 
Submission date May 21, 2010
Last update date May 15, 2019
Contact name Sandeep Nagaraj Wontakal
Organization name Albert Einstein College of Medicine
Department Cell Biology
Lab Dr. Art Skoultchi
Street address 1300 Morris Park Ave Chanin 402
City Bronx
State/province NY
ZIP/Postal code 10461
Country USA
 
Platform ID GPL9250
Series (2)
GSE21950 Genome-wide binding pattern of PU.1 in normal erythroid progenitors and erythroleukemia cells
GSE21953 PU.1 in normal erythroid progenitors and erythroleukemia cells
Relations
SRA SRX021428
BioSample SAMN00014128

Supplementary file Size Download File type/resource
GSM545881_MEL_input_Nov08.bed.gz 82.7 Mb (ftp)(http) BED
SRA Run SelectorHelp
Processed data provided as supplementary file
Raw data are available in SRA

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