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Status |
Public on May 22, 2012 |
Title |
Harvard_ChipSeq_GM12878_ZZZ3_std |
Sample type |
SRA |
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Source name |
GM12878
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Organism |
Homo sapiens |
Characteristics |
lab: Harvard lab description: Struhl - Harvard 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: ZZZ3 antibody antibodydescription: Rabbit Polyclonal anti-human ZZZ3, Immunogen: Synthetic peptide coupled to Ovalbumin (Name PI130, sequence CGNNNGRTTDLKQQSTRESW). Antibody Target: ZZZ3 antibody targetdescription: ZZZ3 contains one ZZ-type zinc finger domain. ZZ type finger domains are named because of their ability to bind two zinc ions. These domains contain 4-6 Cys residues that participate in zinc binding (plus additional Ser/His residues), including a Cys-X2-Cys motif found in other zinc finger domains. These zinc fingers are thought to be involved in protein-protein interactions -they are most likely involved in ligand binding or molecular scaffolding. The structure of the ZZ domain shows that it belongs to the family of cross-brace zinc finger motifs that include the PHD, RING, and FYVE domains. antibody vendorname: Lazlo Tora, Institut de G?n?tique et de Biologie Mol?culaire et Cellulaire antibody vendorid: ZZZ3 control: std control description: Standard input signal for most experiments. control: std control description: Standard input signal for most experiments. controlid: wgEncodeEH000625 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) |
[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 |
SRX150562 |
BioSample |
SAMN01001022 |
Named Annotation |
GSM935483_hg19_wgEncodeSydhTfbsGm12878Zzz3StdSig.bigWig |
Supplementary file |
Size |
Download |
File type/resource |
GSM935483_hg19_wgEncodeSydhTfbsGm12878Zzz3StdPk.narrowPeak.gz |
17.6 Kb |
(ftp)(http) |
NARROWPEAK |
GSM935483_hg19_wgEncodeSydhTfbsGm12878Zzz3StdSig.bigWig |
429.6 Mb |
(ftp)(http) |
BIGWIG |
SRA Run Selector |
Raw data are available in SRA |
Processed data provided as supplementary file |
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