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Sample GSM578566 Query DataSets for GSM578566
Status Public on Aug 31, 2013
Title SLEC-Ba92-Liver-03
Sample type RNA
 
Source name E.coli challenged animal's liver
Organism Papio cynocephalus
Characteristics tissue: Liver
stress: E.coli (serotype B7-086a:K61) challenge
agent: untreated
sepsis stage: n/a
Treatment protocol Papio cyanocephalus baboons were held for 30 days at the OUHSC animal facility. Only healthy tuberculosis free animals with hemoglobin greater than 10 g/dL and white blood cell (WBC) count less than 12,000 were included in the study. Animals were infused with 1x109 live E. coli (LD50 dose) as described before. The time point at which the infusion was started is further indicated as T0, a time point of n hours thereafter referred to as T+n hours. Compstatin was administered as a 10-mg/kg iv. bolus followed by 60μg/kg/min continuous infusion. Three experimental E. coli groups were studied: (i) E. coli challenge only (n=4); (ii) E. coli plus compstatin treatment from T0 to T+8 (n=4; prevention regimen); (iii) E. coli plus compstatin from T+5 to T+11 (n=4; rescue regimen). The control group comprising three animals received saline infusion only.
Growth protocol Live E. coli organisms (serotype B7-086a:K61; American Type Culture Collection, Rockville, MD), stored in the lyophilized state at 4°C after growth in tryptic soybean agar, were reconstituted and used. To eliminate differences due to E. coli strain variations, all animals were infused with E. coli from this single isolate.
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA was performed according to the manufacturer's instructions, RNA was further purified with the Qiagen DNeasyTissue kit (Qiagen, Valencia, CA) and the contaminant genomic DNA was removed with a Qiagen on-column DNase digestion kit. RNA concentrations are determined on a scanning UV/VIS spectrophotometer Nanodrop ND-1000 Spectrophotometer. RNA Quality Assessment by using Agilent 2100 Bioanalyzer Capillary Gel Electrophoresis System.
Label Biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 10 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
 
Hybridization protocol Following fragmentation, 20 ug of cRNA were hybridized using Model 640 hybridization oven for 16 hr at 45C on GeneChip Human Genome Array U133A 2.0. GeneChips were washed and stained in the Affymetrix GeneChip® 450 fluidics station.
Scan protocol GeneChips were scanned using GeneChip® 3000 7G scanner with autoloader (0.51 micron resolution)
Description Gene expression data from E.coli challenged baboon liver
Data processing RMA
 
Submission date Aug 12, 2010
Last update date Aug 31, 2013
Contact name florea lupu
E-mail(s) [email protected]
Phone 405-271-7483
Fax 405-271-7417
Organization name Oklahoma Medical Research Foundation
Street address 825 NE 13th Street
City Oklahoma City
ZIP/Postal code 73104
Country USA
 
Platform ID GPL571
Series (1)
GSE23590 Gene expression data from compstatin treated E.coli-Induced primate sepsis model

Data table header descriptions
ID_REF
VALUE RMA signal intensity

Data table
ID_REF VALUE
1007_s_at 264.529743
1053_at 31.734865
117_at 28.449056
121_at 241.973601
1255_g_at 13.507545
1294_at 123.585916
1316_at 42.202624
1320_at 43.954979
1405_i_at 31.865203
1431_at 8249.706713
1438_at 63.705362
1487_at 369.895693
1494_f_at 4303.406681
1598_g_at 272.461794
160020_at 146.59444
1729_at 198.889236
1773_at 42.226103
177_at 23.83918
179_at 312.555502
1861_at 69.870074

Total number of rows: 22277

Table truncated, full table size 462 Kbytes.




Supplementary file Size Download File type/resource
GSM578566.CEL.gz 2.0 Mb (ftp)(http) CEL
Processed data included within Sample table

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