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Sample GSM663475 Query DataSets for GSM663475
Status Public on Jan 29, 2011
Title Spleen Follicular B cells from B6 mouse #92769
Sample type RNA
 
Source name B6 Spleen Follicular B cells
Organism Mus musculus
Characteristics animal id: B6 mouse #92769
cell type: Spleen Follicular B cells
genetic background: B6
genotype: wild type
Treatment protocol Cells were obtained from control B6 mice or mice transgenic for KLF3 (CD19:KLF3)
Growth protocol Viable spleen follicular B cells and MZB cells were sorted based on C19, CD21 and CD23 expression (sytox_blue_neg, CD19_pos, CD21_int, CD23_pos and sytox_blue_neg, CD19_pos, CD21_high, CD23_neg respectively)
Extracted molecule total RNA
Extraction protocol RNA was extracted using the RNeasy Mini Kit (Qiagen) according to the manufacturer’s protocol. RNA quantification was performed using a spectrophotometer (NanoDrop Technologies) and RNA quality was assessed using the Experion automated electrophoresis system (Bio-Rad).
Label biotin
Label protocol Total RNA was amplified and labeled using the Illumina TotalPrep RNA Amplification kit, which is based on the Eberwine amplification protocol.
 
Hybridization protocol The biotinylated cRNA was hybridized onto Illumina MouseRef-8 BeadChips V2 at 58oC for 20 hrs
Scan protocol Fluoresent array images were collected using Illumina BeadStation 500GX scanner and image intensity data were extracted using Illumina BeadStudio v3.
Description Spleen Follicular B cells from B6 mouse #92769
Data processing Illumina probe data were exported from BeadStudio as raw data and were screened for quality. Samples failing chip visual inspection and control examination were removed. The R software was used to quantile-normalized the probe intensities, and to minimun replace (surrogate-replacement policy) values below backround using the mean backround value of the built-in Illumina probe controls as an alternative to background substraction (which may introduce negative values) to reduce ‘over inflated’ expression ratios in subsequent steps.
 
Submission date Jan 28, 2011
Last update date Jan 29, 2011
Contact name Jean-Philippe Goulet
E-mail(s) jp.goulet@umontreal.ca
Organization name Université de Montréal
Street address C.P. 6128, succursale Centre-ville
City Montréal
State/province Québec
ZIP/Postal code H3X 3J7
Country Canada
 
Platform ID GPL6885
Series (1)
GSE26948 Programming of marginal zone B cell fate by basic krüppel-like factor (BKLF/KLF3)

Data table header descriptions
ID_REF
VALUE quantile normalized log2 intensity

Data table
ID_REF VALUE
ILMN_2607609 11.24198613
ILMN_1238674 6.586654268
ILMN_3062534 7.044518305
ILMN_3140158 9.455499102
ILMN_2674533 9.954796062
ILMN_2680307 6.741524164
ILMN_2935307 7.042858151
ILMN_2910106 8.612306178
ILMN_1215893 9.085858719
ILMN_2732092 7.757892105
ILMN_2603725 11.55935713
ILMN_2664884 7.198750117
ILMN_3003575 6.960201993
ILMN_1229397 6.423474284
ILMN_1225873 6.656197137
ILMN_2899591 9.107269284
ILMN_2658355 6.833597657
ILMN_2682763 6.898524908
ILMN_2521511 6.716903672
ILMN_2691286 6.719872272

Total number of rows: 25697

Table truncated, full table size 624 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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