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GEO help: Mouse over screen elements for information. |
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Status |
Public on May 22, 2012 |
Title |
Stanford_ChipSeq_K562_COREST_(sc-30189)_IgG-rab |
Sample type |
SRA |
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Source name |
K562
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Organism |
Homo sapiens |
Characteristics |
lab: Stanford lab description: Snyder - Stanford University datatype: ChipSeq datatype description: Chromatin IP Sequencing cell: K562 cell organism: human cell description: leukemia, "The continuous cell line K-562 was established by Lozzio and Lozzio from the pleural effusion of a 53-year-old female with chronic myelogenous leukemia in terminal blast crises." - ATCC cell karyotype: cancer cell lineage: mesoderm cell sex: F treatment: None treatment description: No special treatment or protocol applies antibody: COREST_(sc-30189) antibody antibodydescription: Rabbit polyclonal, epitope corresponding to amino acids 246-310 mapping within an internal region of CoREST of human origin recommended for detection of CoREST of mouse, rat and human origin. Antibody Target: COREST (sc30189) antibody targetdescription: Essential component of the BHC complex, a corepressor complex that represses transcription of neuron-specific genes in non-neuronal cells. In the BHC complex, it serves as a molecular beacon for the recruitment of molecular machinery, including MeCP2 and SUV39H1, that imposes silencing across a chromosomal interval. Plays a central role in demethylation of Lys-4 of histone H3 by promoting demethylase activity of KDM1A on core histones and nucleosomal substrates. antibody vendorname: Santa Cruz Biotech antibody vendorid: sc-30189 control: IgG-rab control description: Input signal from Normal Rabbit IgG ChIP-seq. control: IgG-rab control description: Input signal from Normal Rabbit IgG ChIP-seq. controlid: wgEncodeEH001795 replicate: 1
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Biomaterial provider |
ATCC
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Treatment protocol |
None
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Growth protocol |
K562_protocol.pdf
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Extracted molecule |
genomic DNA |
Extraction protocol |
Instrument model unknown. ("Illumina Genome Analyzer" specified by default). For more information, see http://genome.ucsc.edu/cgi-bin/hgTrackUi?db=hg19&g=wgEncodeSydhTfbs
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Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina Genome Analyzer |
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Data processing |
http://genome.ucsc.edu/cgi-bin/hgTrackUi?db=hg19&g=wgEncodeSydhTfbs
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Submission date |
May 22, 2012 |
Last update date |
May 15, 2019 |
Contact name |
ENCODE DCC |
E-mail(s) |
[email protected]
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Organization name |
ENCODE DCC
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Street address |
300 Pasteur Dr
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City |
Stanford |
State/province |
CA |
ZIP/Postal code |
94305-5120 |
Country |
USA |
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Platform ID |
GPL9052 |
Series (2) |
GSE31477 |
ENCODE Transcription Factor Binding Sites by ChIP-seq from Stanford/Yale/USC/Harvard |
GSE51334 |
DNA replication-timing boundaries separate stable chromosome domains with cell-type-specific functions |
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Relations |
SRA |
SRX150518 |
BioSample |
SAMN01000978 |
Named Annotation |
GSM935439_hg19_wgEncodeSydhTfbsK562Corestsc30189IggrabSig.bigWig |
Supplementary file |
Size |
Download |
File type/resource |
GSM935439_hg19_wgEncodeSydhTfbsK562Corestsc30189IggrabPk.narrowPeak.gz |
1.9 Mb |
(ftp)(http) |
NARROWPEAK |
GSM935439_hg19_wgEncodeSydhTfbsK562Corestsc30189IggrabSig.bigWig |
329.1 Mb |
(ftp)(http) |
BIGWIG |
SRA Run Selector |
Raw data are available in SRA |
Processed data provided as supplementary file |
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