GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
Sample GSM1094652 Query DataSets for GSM1094652
Status Public on Mar 07, 2014
Title 57_LR_SN
Sample type RNA
Source name Low responder, stimulated plus natalizumab treatment
Organism Homo sapiens
Characteristics subject: 57
disease status: multiple sclerosis (MS)
gender: male
age: 42
natalizumab responder type: low
tissue: whole blood
cell type: CD4+ T cells
treatment: natalizumab
Treatment protocol PBMCs were collected from 8 high responders (HR) and 8 low responders (LR) to natalizumab treatment and were stimulated with anti-CD3/-CD28 antibodies (0.1µg/mL, R&D Systems, Minneapolis, MN, USA), with or without addition of natalizumab (50µg/mL) and cultured for 48h.
Extracted molecule total RNA
Extraction protocol Total CD4+ T cells were enriched by MACS negative sorting (Miltneyi Biotec, Auburn, CA, USA). Total RNA was extracted using TRIreagent (Cincinnati, OH, USA).
Label Cy3
Label protocol Cyanine-3 (Cy3) labeled cRNA was prepared from 15ng total RNA using a Low Input Quick Amp Labeling Kit (Agilent Technologies, Palo Alto, Calif, USA) according to the manufacturer's instructions, followed by RNeasy column purification (QIAGEN, Valencia, CA). Dye incorporation and cRNA yield were checked with the NanoDrop ND-1000 Spectrophotometer.
Hybridization protocol 600 ng of Cy3-labelled cRNA (specific activity >6 pmol Cy3/ug cRNA) was fragmented at 60°C for 30 minutes in a total volume of 25ul following the manufacturer's instructions. On completion of the fragmentation reaction, 25ul of 2x Agilent hybridization buffer was added to the fragmentation mixture and hybridized to Agilent Whole Human Genome Oligo Microarrays (G4851A) for 17 hours at 65°C in a rotating Agilent hybridization oven. After hybridization, microarrays were washed 1 minute at room temperature with GE Wash Buffer 1 (Agilent) and 1 minute with 37°C GE Wash buffer 2 (Agilent), then dried immediately by brief centrifugation.
Scan protocol Slides were scanned immediately after washing on the Agilent DNA Microarray Scanner using one color scan setting for 8x60k array slides.
Data processing The scanned images were analyzed with Feature Extraction Software (Agilent). Features flagged in Feature Extraction as Feature Non-uniform outliers were excluded. 24 samples were analyzed using the GPL16083 Platform, and 8 were analyzed using the GPL16705 Platform. Probes not detectable on either the GPL16083 or GPL16705 Platform were excluded. In addition, only probes common to both Platforms are presented. The raw data was extracted using GeneSpring GX software and was quantile normalized using the limma package in the R program. Batch effects were normalized using ComBat.
Submission date Mar 07, 2013
Last update date Mar 07, 2014
Contact name Hui Wang
Organization name Xuzhou Medical University
Street address 209 Tongshan Rd
City Xuzhou
State/province Jiangsu
ZIP/Postal code 224001
Country China
Platform ID GPL17077
Series (2)
GSE44964 Integrated genomic and prospective clinical studies show the importance of modular pleiotropy for disease susceptibility, diagnosis and treatment (dataset 2)
GSE44966 Integrated genomic and prospective clinical studies show the importance of modular pleiotropy for disease susceptibility, diagnosis and treatment

Data table header descriptions
VALUE Quantile- and ComBat-normalized signal intensity (natural log transformed)

Data table
A_19_P00315452 1.99392009
A_19_P00315459 3.649861487
A_19_P00315482 1.379266918
A_19_P00315492 2.09683228
A_19_P00315493 3.777357759
A_19_P00315502 0.669020428
A_19_P00315506 4.971515685
A_19_P00315518 0.803529961
A_19_P00315519 0.835040275
A_19_P00315524 7.870379882
A_19_P00315528 5.255765887
A_19_P00315529 5.40016103
A_19_P00315538 0.743000923
A_19_P00315541 1.420639655
A_19_P00315543 2.035885917
A_19_P00315550 2.960911695
A_19_P00315551 3.954838027
A_19_P00315554 0.989186204
A_19_P00315581 5.52819182
A_19_P00315583 2.702678266

Total number of rows: 35649

Table truncated, full table size 877 Kbytes.

Supplementary file Size Download File type/resource
GSM1094652_US91203659_253949410545_S01_GE1_107_Sep09_2_4.txt.gz 3.0 Mb (ftp)(http) TXT
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap