NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM560857 Query DataSets for GSM560857
Status Public on Jan 01, 2013
Title NOD2wt_0h_MDP_biological replicate 3
Sample type RNA
 
Source name HEK-293
Organism Homo sapiens
Characteristics cell line: HEK-293
genotype: NOD2 wt
stimulation: Muramyl-dipeptide (MDP) 10 µg/ml
time point: 0 h
Treatment protocol FLP-IN HEK 293-NOD2wt, HEK 293-NOD2L1007fsinsC and HEK 293mock cells were cultivated in medium without FCS for 7 h before stimulation with 10 µg/ml MDP for 0h, 2h and 6h. Cells were harvested simultaneously.
Growth protocol NOD2wt and NOD2-L1007fsinsC expressing cells were generated with the FLP-IN system (Invitrogen, Carlsbad, CA, USA). HEK 293 cells containing the recombination site were purchased from Invitrogen. Wildtype and mutated NOD2 were inserted to the genomic recombination site by FLP-recombinase enzyme. A control cell line was generated by transfecting an empty mock vector. All stable cell lines were selected for Hygromycin B resistance and consequently cultured in MEM + 10 % FCS + 1% Penicillin/Streptomycin + 50 μg/ml Hygromycin B (Invitrogen).
Extracted molecule total RNA
Extraction protocol RNA was isolated using the RNeasy Kit (Qiagen)
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 1 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
 
Hybridization protocol Following fragmentation, cRNA were hybridized for 16 hr at 45C on Affymetrix Human Genome U133 Plus 2.0 Array in a Affymetrix Hybridization Oven 640. GeneChips were washed and stained in the Affymetrix Fluidics Station.
Scan protocol GeneChips were scanned using the Affymetrix GeneChip Scanner 3000.
Description RNA from cell culture with different NOD2 genotypes
Data processing The data were analyzed with Gene Chip Operating Software 1.1. Represents the relative level of expression of a transcript. The median of the data is identified and each datum is weighted by how far it is from the median using One-step Tukey's Biweight Algorithm. A weighted mean is then calculated.
 
Submission date Jun 29, 2010
Last update date Jan 01, 2013
Contact name Susanne Billmann
Organization name Institute of Clinical Molecular Biology Christian-Albrechts-Universität Kiel
Street address Schittenhelmstraße 12
City Kiel
ZIP/Postal code D-24105
Country Germany
 
Platform ID GPL570
Series (1)
GSE22611 NOD2 and desease associated variant NOD2-L1007fsinsC dependent genomewide transcriptional regulation in stable Flp-In HEK cells

Data table header descriptions
ID_REF
VALUE GeneChip Operating Software 1.1 signal
ABS_CALL

Data table
ID_REF VALUE ABS_CALL
1007_s_at 1735.7 P
1053_at 4922.2 P
117_at 161.4 A
121_at 1513.1 P
1255_g_at 66.8 A
1294_at 320.5 A
1316_at 326.8 P
1320_at 28.6 A
1405_i_at 7.7 A
1431_at 71.7 A
1438_at 105.4 A
1487_at 692.3 A
1494_f_at 170.8 A
1552256_a_at 1887.3 P
1552257_a_at 2736.8 P
1552258_at 184.5 A
1552261_at 79.1 A
1552263_at 444.2 P
1552264_a_at 1097.1 P
1552266_at 97.3 A

Total number of rows: 54675

Table truncated, full table size 984 Kbytes.




Supplementary file Size Download File type/resource
GSM560857.CEL.gz 7.9 Mb (ftp)(http) CEL
Processed data included within Sample table

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