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Sample GSM1863298 Query DataSets for GSM1863298
Status Public on Oct 30, 2015
Title RNA-P1 subpopulation [BN148_P1]
Sample type RNA
 
Source name in vitro activation of naive B cell from normal blood
Organism Homo sapiens
Characteristics subpopulation labeling: DAPI neg CFSE low CD38 high
day of isolation: D6
Treatment protocol Stimulation cocktail 1 (2,6 µg/ml Fab'2 anti-Ig, 100 ng/ml CD40 Ligand, 1 µg/ml CpG ODN 2006 and 50 U/ml IL2) for 4 days then differentiation cocktail 2 (50 U/ml IL2, 5 ng/ml IL4, 10 ng/ml IL10) for 2 days (Le Gallou et al., 2012)
Growth protocol Naive B cells from healthy donors were purified using magnetic cell separation (Miltenyi Biotech), CFSE-labeled and cultured at 7.5.105 cells/ml for 4 days with cocktail 1. Activated B cells were then washed and further cultured at 4.105 with cocktail 2 (Le Gallou et al., 2012)
Extracted molecule total RNA
Extraction protocol RNA was extracted using the AllPrep DNA/RNA mini kit (Qiagen) after cell-sorting of the different subpopulations (FACS Aria, BD Biosciences).
Label biotin
Label protocol 150ng of each of the samples with RIN value >7 were converted to biotinylated cRNA with the Illumina TotalPrep-96 RNA Amplification Kit (Ambion) using a standard T7-based amplification protocol
 
Hybridization protocol Following fragmentation, 7.5 ug of cRNA were hybridized on HG-U219 arrays in 120ul volume/well. The GeneTitan Hybridization, Wash and Stain kit (Affymetrix) was used for preparing hybridization mixes and automated processing of 96-array plates on the GeneTitan Instrument (Affymetrix)
Scan protocol HG-U219 Array Plates were scanned on the GeneTitan instrument (Affymetrix) imaging device according to manufacturer's instructions
Description BN148_P1.CEL
Data processing Raw data were normalized with the Robust Multichip Analysis (RMA) algorithm using BioConductor Affy Package
 
Submission date Aug 28, 2015
Last update date Oct 30, 2015
Contact name Gilles Salbert
E-mail(s) gilles.salbert@univ-rennes1.fr
Phone +33 223 236 625
Organization name University of Rennes 1
Department Biology
Lab UMR6290 CNRS
Street address Avenue du Général Leclerc
City Rennes
ZIP/Postal code 35042
Country France
 
Platform ID GPL13667
Series (2)
GSE72497 Cell cycle-dependent reconfiguration of the DNA (hydroxy) methylome during terminal differentiation of human B cells into plasma cells [expression array]
GSE72498 Cell cycle-dependent reconfiguration of the DNA (hydroxy) methylome during terminal differentiation of human B cells into plasma cells

Data table header descriptions
ID_REF
VALUE Log2 RMA signal estimates obtained using the affy package from www.bioconductor.org.

Data table
ID_REF VALUE
11715100_at 5.781899352
11715101_s_at 6.885806965
11715102_x_at 5.886935983
11715103_x_at 3.731589061
11715104_s_at 3.628398231
11715105_at 4.001946208
11715106_x_at 4.210567355
11715107_s_at 3.747201414
11715108_x_at 4.349480252
11715109_at 3.819160853
11715110_at 3.762890073
11715111_s_at 4.774114639
11715112_at 3.914967812
11715113_x_at 3.927640332
11715114_x_at 4.152480836
11715115_s_at 3.3200294
11715116_s_at 3.682794954
11715117_x_at 4.183757282
11715118_s_at 4.851971354
11715119_s_at 4.000869666

Total number of rows: 49386

Table truncated, full table size 1225 Kbytes.




Supplementary file Size Download File type/resource
GSM1863298_BN148_P1.CEL.gz 2.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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