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Sample GSM318571 Query DataSets for GSM318571
Status Public on Sep 06, 2008
Title Primary ovine microglia PrPC bio repB tech rep1 (Mock12B.2.1)
Sample type RNA
 
Source name primary ovine microglial cells sham inoculated with PrPC
Organism Ovis aries
Characteristics Primary ovine microglia
Treatment protocol Primary microglia were passed into 6-well plates and grown to approximately 60% confluency. Microglia were rinsed once with PBS and then overlaid with 200 μl of a 1/20 dilution of either the Rov9Sc lysate (Inoc A, B, and C) or the Rov9C lysate (Mock A, B, and C) in OPTI-MEM. All replicates (A, B, and C) of both treatment groups (Inoc and Mock) were incubated for six hours and then 200 μl of OMEM were added to each well. Following an additional two days of incubation, 0.5 ml of OMEM was added to each well, and microglia were incubated for four days at which time they were expanded into 25-cm2 tissue culture flasks. Microglia were fed every three to four days with OMEM as necessary and serially passed 1/5 after reaching confluence.
Growth protocol Microglial cells were cultured using standard techniques, in OPTI-MEM I Reduced Serum Medium (Invitrogen, Carlsbad, CA) supplemented with 10% heat-inactivated FBS, 2 mM L-glutamine, 10 IU/ml of penicillin, and 10 mg/ml of streptomycin.
Extracted molecule total RNA
Extraction protocol QIAshredder spin columns (Qiagen, Valencia, CA) followed by Qiagen RNeasy mini spin columns
Label biotin
Label protocol 10ug total RNA labelled according to Affymetrix one cycle labelling protocol
 
Hybridization protocol Affymetrix hybridization protocols; Affymetrix GeneChip Fluidics Station 450
Scan protocol Affymetrix GeneChip Scanner 300 7G
Description Mock infected primary ovine microglial cells
Data processing All analyses of microarray data were conducted using Bioconductor for R (www.R-project.org). Data were normalized using the Micro Array Suite 5.0 (MAS5) algorithm. The ComBat algorithm (http://statistics.byu.edu/johnson/ComBat/) was used to correct for batch effect.
 
Submission date Sep 05, 2008
Last update date Sep 05, 2008
Contact name James Stanton
Organization name Washington State University
Street address PO Box 647034
City Pullman
State/province WA
ZIP/Postal code 99164-7034
Country USA
 
Platform ID GPL2112
Series (1)
GSE12688 Expression profiling of prion accumulating ovine microglia

Data table header descriptions
ID_REF
VALUE MAS5 signal intensity, corrected for batch effect using ComBat

Data table
ID_REF VALUE
AFFX-BioB-3_at 7.65729982795274
AFFX-BioB-5_at 7.58097803314679
AFFX-BioB-M_at 8.34387746538278
AFFX-BioC-3_at 9.53127504619605
AFFX-BioC-5_at 9.11260513645657
AFFX-BioDn-3_at 10.7402311328758
AFFX-BioDn-5_at 10.2583194602087
AFFX-Bt-A00196-1_s_at 4.55078952185523
AFFX-Bt-AB076373-1_at 4.5278255551025
AFFX-Bt-actin-3_at 7.21864042492587
AFFX-Bt-actin-5_at 4.41610343018298
AFFX-Bt-actin-M_at 4.54012990527209
AFFX-Bt-AF292559-1_at 4.24805280651538
AFFX-Bt-AF292559-2_s_at 4.10744328429374
AFFX-Bt-AF292559-3_s_at 4.0821562356651
AFFX-Bt-AF292559-4_s_at 4.17591107941416
AFFX-Bt-AF292560-1_s_at 4.07715859783335
AFFX-Bt-AF298789-1_at 4.06735595970235
AFFX-Bt-AF323980-1_at 4.01235246227335
AFFX-Bt-AJ002682-1_s_at 4.64788790239643

Total number of rows: 24128

Table truncated, full table size 793 Kbytes.




Supplementary file Size Download File type/resource
GSM318571.CEL.gz 2.0 Mb (ftp)(http) CEL
Processed data included within Sample table

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