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Sample GSM351519 Query DataSets for GSM351519
Status Public on Feb 18, 2009
Title MKO1_minHGF
Sample type RNA
 
Source name liver; c-Met knockout mouse; unstimulated
Organism Mus musculus
Characteristics Backgroud:C57/BL6, Gender:male, Age:8-10 weeks
Treatment protocol For gene array analysis c-MetDhepa and c-MetloxP/loxP controls were stimulated for 2 hours with 2µg recombinant mouse HGF.Three animals per group were treated in parallel, before and after i.p. injection of recombinant HGF or NaCl.
Growth protocol C-MetloxP/loxP animals were first crossed with albumin/AFP promoter/enhancer13 (Alfp-Cre) or albumin promoter-Cre transgenic animals (Alb-Cre). The Alfp-Cre animals express Cre-recombinase during embryonal development, while Alb-Cre mice start to express Cre 2 weeks after birth.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from cryopreserved liver tissue by using peqGold RNAPure (PeqLab, Erlangen, Germany).
Label biotin
Label protocol The Affymetrix GeneChip RNA One cycle Amplification Kit was used to prepare labelled cRNA from 5 ug of total RNA. The protocol was conducted using the reagents provided by Affymetrix in the One-Cycle cDNA synthesis kit (P/N 900431), One-Cycle IVT labelling kit (P/N 90449) and GeneChip Sample Cleanup Module (P/N 900371). A detailed description can be found in the Genechip Expression Analysis Technical Manual, section 2 (Eukaryotic Sample and Array Processing), chapter 1 (Eukaryotic Target Preparation) (P/N 701025, revision 6).
 
Hybridization protocol Hybridisation of 10ug cRNA was done overnight for 16 hours at 45ºC in a Hybridisation Oven 640 (Affymetrix). The protocol is conducted as described in the Genechip Expression Analysis Technical Manual, section 2 (Eukaryotic Sample and Array Processing), chapter 2 (Eukaryotic Target Hybridization) (P/N 701027, revision 5).
Scan protocol Arrays were scanned on an Affymetrix 3000 7G scanner, as described in the Genechip Expression Analysis Technical Manual, section 2 (Eukaryotic Sample and Array Processing), chapter 2 (Eukaryotic Arrays: Washing, Staining and Scanning (P/N 701028, revision 5).
Description A85_07_minHGF_MKO1
Data processing Expression estimates were calculated using GCRMA, employing the empirical Bayes approach for background adjustment.
 
Submission date Dec 16, 2008
Last update date Feb 18, 2009
Contact name Guido Hooiveld
E-mail(s) guido.hooiveld@wur.nl
Organization name Wageningen University
Department Div. Human Nutrition & Health
Lab Nutrition, Metabolism & Genomics Group
Street address HELIX, Stippeneng 4
City Wageningen
ZIP/Postal code NL-6708WE
Country Netherlands
 
Platform ID GPL7546
Series (1)
GSE13992 c-Met confers protection against chronic liver tissue damage and fibrosis progression after bile-duct-ligation in mice

Data table header descriptions
ID_REF
VALUE GCRMA signal (unlogged)

Data table
ID_REF VALUE
100009600_at 2.638047577
100012_at 3.165984151
100017_at 45.32684227
100019_at 5.392694638
100034251_at 221.6669643
100036521_at 162.4846683
100037258_at 454.906158
100037278_at 3.721068223
100038570_at 4.020741097
100038635_at 3.841474789
100038680_at 2.624257822
100038887_at 1468.573133
100038959_at 3.5667565
100039026_at 8.443586543
100039027_at 3.827603348
100039094_at 2.997161248
100039235_at 3.334020491
100039282_at 4.254839012
100039284_at 3.876553144
100039307_at 5.340506561

Total number of rows: 16539

Table truncated, full table size 343 Kbytes.




Supplementary file Size Download File type/resource
GSM351519.CEL.gz 3.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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