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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_GM12878_SIN3A_(NB600-1263)_IgG-mus |
Sample type |
SRA |
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Source name |
GM12878
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Organism |
Homo sapiens |
Characteristics |
lab: Stanford lab description: Snyder - Stanford University datatype: ChipSeq datatype description: Chromatin IP Sequencing cell: GM12878 cell organism: human cell description: B-lymphocyte, lymphoblastoid, International HapMap Project - CEPH/Utah - European Caucasion, Epstein-Barr Virus cell karyotype: normal cell lineage: mesoderm cell sex: F treatment: None treatment description: No special treatment or protocol applies antibody: SIN3A_(NB600-1263) antibody antibodydescription: Rabbit polyclonal, Immunogen: Synthetic peptide: MKRRLDDQESDVYAAQQRR, corresponding to amino acids 1-19 of Mouse mSin3A. Antibody Target: SIN3A (NB600-1263) antibody targetdescription: Mammalian Sin 3 (mSin 3) is closely related to the yeast SIN3 repressor protein involved in the transcriptional repression of many genes. Containing 4 paired amphipathic helix domains (PAH domains), mSin 3A and mSin 3B have been shown to directly interact with several other transcriptional repressor proteins including HDAC 1, HDAC 2, RbAp 46, the methyl CpG binding protein MeCP 2, the Mad/Max heterodimer, and the corepressors silencing mediator of retinoic acid & thyroid hormone receptor (SMRT) and nuclear receptor corepressor (N-CoR). antibody vendorname: Novus Biologicals antibody vendorid: NB600-1263 control: IgG-mus control description: Input signal from Normal Mouse IgG ChIP-seq. control: IgG-mus control description: Input signal from Normal Mouse IgG ChIP-seq. controlid: wgEncodeEH000706 replicate: 1
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Biomaterial provider |
Coriell; http://ccr.coriell.org/Sections/Search/Search.aspx?PgId=165&q=GM12878
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Treatment protocol |
None
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Growth protocol |
GM12878_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) |
encode-help@lists.stanford.edu
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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 |
SRX150411 |
BioSample |
SAMN01000872 |
Named Annotation |
GSM935331_hg19_wgEncodeSydhTfbsGm12878Sin3anb6001263IggmusSig.bigWig |
Supplementary file |
Size |
Download |
File type/resource |
GSM935331_hg19_wgEncodeSydhTfbsGm12878Sin3anb6001263IggmusPk.narrowPeak.gz |
341.6 Kb |
(ftp)(http) |
NARROWPEAK |
GSM935331_hg19_wgEncodeSydhTfbsGm12878Sin3anb6001263IggmusSig.bigWig |
174.9 Mb |
(ftp)(http) |
BIGWIG |
SRA Run Selector |
Raw data are available in SRA |
Processed data provided as supplementary file |
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