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Sample GSM318572 Query DataSets for GSM318572
Status Public on Sep 06, 2008
Title Primary ovine microglia PrPC bio repB tech rep2 (Mock12B.2.2)
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 7.4918323162887
AFFX-BioB-5_at 7.57514263280244
AFFX-BioB-M_at 8.14095147840675
AFFX-BioC-3_at 9.39052179583969
AFFX-BioC-5_at 8.97996668779469
AFFX-BioDn-3_at 10.7133565082751
AFFX-BioDn-5_at 10.2253586145631
AFFX-Bt-A00196-1_s_at 4.15807129587282
AFFX-Bt-AB076373-1_at 4.24284631449216
AFFX-Bt-actin-3_at 7.44706232496952
AFFX-Bt-actin-5_at 4.69773329137906
AFFX-Bt-actin-M_at 5.480611506568
AFFX-Bt-AF292559-1_at 4.1123374395828
AFFX-Bt-AF292559-2_s_at 4.5486622023079
AFFX-Bt-AF292559-3_s_at 3.97060429163492
AFFX-Bt-AF292559-4_s_at 4.58284150611374
AFFX-Bt-AF292560-1_s_at 4.11235250234767
AFFX-Bt-AF298789-1_at 4.06876734285714
AFFX-Bt-AF323980-1_at 4.02223631622194
AFFX-Bt-AJ002682-1_s_at 4.97551247755908

Total number of rows: 24128

Table truncated, full table size 793 Kbytes.




Supplementary file Size Download File type/resource
GSM318572.CEL.gz 2.0 Mb (ftp)(http) CEL
Processed data included within Sample table

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