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Sample GSM1567718 Query DataSets for GSM1567718
Status Public on Dec 18, 2014
Title AIL-G4-354
Sample type RNA
 
Source name SKIN
Organism Mus musculus
Characteristics strain: AIL
disease status: HEALTHY
eba severity score: 0
onset week: 0
Treatment protocol Experimental EBA was induced by immunization with an immune-dominant peptide within the murine NC1 domain of Collagen type VII (GST-mCOL7C) as previously described (Ludwig et al. 2011). In total, 600 mice of the AIL were immunized out of which 100 mice were randomly selected for miRNA expression profiling. Mice were evaluated every 4th week after immunization regarding their development and extent of skin disease, following an established scoring system for a total period of 12 weeks (Sitaru et al. 2006). Murine skin tissues were obtained for analysis at the end of the experiment.
Growth protocol The outbred four-way autoimmune-prone advanced intercross line (AIL) was generated (in our group) from the parental mouse strains BXD2/TyJ, MRL/MpJ, NZM2410/J and CAST/EiJ (Asghari et al. 2011; Ludwig et al. 2012; Srinivas et al. 2013). All strains were purchased from The Jackson Laboratory (Bar Harbor, ME). The four inbred strains were intercrossed following an equal strain and sex distribution. First generation (G1) offspring mice were then mated based on their parental origin to generate G2 mice in order to maintain an equal distribution of the original strain alleles across the genome. The same procedure was applied for intercrossing G2 and G3 mice. At least 50 breeding pairs were used for each successive generation of mice. Animals were held under pathogen free conditions at a 12-hour light/dark cycle with food and water ad libitum.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from skin tissue and processed as previously described using the Flash Tag Biotin HSR RNA labeling kit
Label biotin
Label protocol according to the manufacturing guidelines (Affymetrix)
 
Hybridization protocol according to the manufacturing guidelines (Affymetrix)
Scan protocol GeneChips were scanned using the Affymetrix GeneChip Scanner 3000
Description total RNA from 6 month old mice in G4 advance inter cross line
Data processing R bioconductor 2.0
 
Submission date Dec 17, 2014
Last update date Dec 18, 2014
Contact name Saleh M. Ibrahim
E-mail(s) Saleh.Ibrahim@uksh.de
Phone +49 451 500 5250
Organization name Universität zu Lübeck
Department Dermatology
Street address Ratzeburger Allee 160
City Lübeck
State/province Schleswig-Holstein
ZIP/Postal code 23562
Country Germany
 
Platform ID GPL8786
Series (1)
GSE64276 Dissecting the genetics of cutaneous miRNA in a mouse model of autoimmune bullous disease

Data table header descriptions
ID_REF
VALUE RMA normalized

Data table
ID_REF VALUE
14q-0_st 0.45568808
14qI-1_st 1.0962642768
14qI-2_st 0.4163939807
14qI-3_x_st 0.4835763717
14qI-4_st 1.1181443052
14qI-4_x_st 0.8720331697
14qI-5_st 0.4183764785
14qI-6_st 0.6197535457
14qI-6_x_st 0.9322553045
14qI-7_st 1.1668435419
14qI-8_st 0.6543700292
14qI-8_x_st 0.7855111137
14qI-9_x_st 0.554595623
14qII-10_st 0.5169432777
14qII-11_st 0.9752285422
14qII-11_x_st 0.6350636032
14qII-12_st 0.7390921458
14qII-12_x_st 0.5855232089
14qII-13_st 0.8517938092
14qII-14_st 0.8858051728

Total number of rows: 7815

Table truncated, full table size 219 Kbytes.




Supplementary file Size Download File type/resource
GSM1567718_2011-06-24_Ibrahim_354_miRNA-1_0_2Xgain_.CEL.gz 137.7 Kb (ftp)(http) CEL
Processed data included within Sample table

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