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Sample GSM506721 Query DataSets for GSM506721
Status Public on Nov 15, 2010
Title Proliferating 4
Sample type RNA
 
Source name CFSE stained, proliferating, CD19+ cells from EBV-infected PBMCs
Organism Homo sapiens
Characteristics ebv staus: infected, proliferating
cell type: CD19+ B cells, EBV-infected, sorted
day post infection or extraction: 6
Treatment protocol Infected cells were incubated with EBV for 1h at 37 C. CFSE treatment was performed as described (Quah et al, Nature Protocols 2007).
Growth protocol Infected cells (PBMCs) were maintained in RPMI 1640 + 15% FCS + cyclosporin A + Pen/Strep
Extracted molecule total RNA
Extraction protocol CD19+ B cells were purified from PBMC using the BD iMag Negative Isolation Kit (BD #558007). Total RNA was isolated via miRvana organic extraction (Ambion Inc) according to manufacturer's protocol
Label biotin
Label protocol cDNA preparation, labeling, fragmentation performed with Gene Chip cDNA synthesis/amplification kit (Affymetrix # 900673) and Exon Array Labeling kit (Affymetrix #900671)
 
Hybridization protocol Hybridization targets were prepared from totalRNA and hybridized to GeneChip HuEx 1.0 ST arrays according to standard Affymetrix (Santa Clara,CA) GeneChip HuEx 1.0 ST and GeneChip Hybridization, Wash, and Stain protocols
Scan protocol GeneChip Scanner 3000 7G with GeneChip Fluidics Station 450
Description Prolif4_1743_4013_20995_Donor3_EBV_prolif_HuEx-1+0-st-v1.CEL
Data processing Raw .CEL data was normailized and consolidated into a total .GCT metadata file via ExpressionFileCreator RMA normalization of the 12 .CEL files in GenePattern
 
Submission date Feb 04, 2010
Last update date Oct 29, 2010
Contact name Luftig Laboratory
E-mail(s) jpt9@duke.edu, micah.luftig@duke.edu, pavel.nikitin@gmail.com
Phone 9196683123
Organization name Duke University
Department MGM
Lab Luftig Lab
Street address 220 CARL Bldg Duke U Med Center
City Durham
State/province NC
ZIP/Postal code 27710
Country USA
 
Platform ID GPL5188
Series (1)
GSE20200 Exon-Level Expression Data from Primary B Cells, Early Proliferating EBV-infected B Cells and Lymphoblastoid Cell Lines

Data table header descriptions
ID_REF
VALUE RMA normalized (GenePattern) signal intensity

Data table
ID_REF VALUE
2315101 47.9838459093025
2315102 120.905948153278
2315103 109.618547260480
2315104 111.52921869507
2315105 16.0873716836274
2315107 144.003063530192
2315108 83.9776771470626
2315110 108.440500226705
2315112 18.3317202942711
2315114 18.9547254402531
2315116 89.9134271180021
2315118 332.629136019499
2315120 185.561995738550
2315122 124.672179653368
2315124 104.052284482467
2315126 13.9129188429033
2315127 5.20270470530306
2315128 3.19628507801882
2315130 3.76496778907754
2315131 4.20281913586149

Total number of rows: 1432154

Table truncated, full table size 34840 Kbytes.




Supplementary file Size Download File type/resource
GSM506721.CEL.gz 22.7 Mb (ftp)(http) CEL
Processed data included within Sample table

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