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Sample GSM685985 Query DataSets for GSM685985
Status Public on Apr 15, 2011
Title Severe rep6 (retina)
Sample type RNA
 
Source name Retina severe glaucoma
Organism Mus musculus
Characteristics phenotype: severe glaucoma
gender: female
strain: DBA/2J
tissue: retina
age: 10.5 months
Growth protocol All mice were housed in a 14 h light to 10 h dark cycle
Extracted molecule total RNA
Extraction protocol For tissue harvesting, mice were anesthetized and the left eye was dissected free, and the cornea and lens removed. The optic nerve was cut close to the back of the eye. The optic nerve head was excised using a sharpened 1mm glass capillary centered over the optic nerve and immediately placed in RNAlater® (Qiagen). A small portion of central retina as well as a small portion of choroid and sclera are included in this tissue. This tissue is substantially enriched for the glial lamina. The retina (containing no optic nerve head) was then dissected free from the back of the eye and placed in a separate vial containing RNAlater (Ambion, Austin TX) and stored at 4oC until required. The process was repeated for the right eye. Dissection of each eye was completed in ≤5 minutes (10 minutes per mouse)
Label biotin
Label protocol Biotin-labeled cDNA was synthesized separately from 20ng of each total RNA sample per the manufacturer’s protocols (Ovation™ Biotin System (NuGEN, San Carlos, CA). 2.5 μg of each biotin-labeled and fragmented cDNA sample was then hybridized onto Mouse Genome 430 v2.0 GeneChip™ arrays (Affymetrix, Santa Clara, CA).
 
Hybridization protocol Hybridization and post-hybridization staining and washing were performed according to manufacturer's protocols using the Fluidics Station 450 instrument (Affymetrix).
Scan protocol The arrays were scanned with a GeneChipTM Scanner 3000 laser confocal slide scanner
Description Retina R115844
Data processing The images were quantified using GeneChipTM Operating Software (GCOS) v1.2. Probe level data were imported into the R statistical software environment (http://www.r-project.org) and expression values for each probe set on the array were summarized using the Robust MultiChip Average (RMA) method with quantile normalization in the R/affy package
 
Submission date Mar 04, 2011
Last update date Apr 15, 2011
Contact name Gareth Rhys Howell
E-mail(s) gareth.howell@jax.org
Phone 207 288 6572
Fax 207 288 6078
Organization name The Jackson Laboratory
Street address 600 Main Street
City Mount Desert
ZIP/Postal code 04609
Country USA
 
Platform ID GPL1261
Series (1)
GSE26299 Gene expression profiling in DBA/2J glaucoma

Data table header descriptions
ID_REF
VALUE RMA quantile-normalized value

Data table
ID_REF VALUE
1415670_at 7.14248182
1415671_at 9.05471155
1415672_at 9.74853807
1415673_at 7.36277698
1415674_a_at 7.77320283
1415675_at 8.73752707
1415676_a_at 9.63097734
1415677_at 6.70935049
1415678_at 12.0901442
1415679_at 9.14472629
1415680_at 6.99315599
1415681_at 7.52336463
1415682_at 7.62204153
1415683_at 8.05133781
1415684_at 7.43075776
1415685_at 8.39376374
1415686_at 11.4121357
1415687_a_at 10.3243018
1415688_at 10.1965867
1415689_s_at 7.10383221

Total number of rows: 45101

Table truncated, full table size 982 Kbytes.




Supplementary file Size Download File type/resource
GSM685985_GC_430_2_R115844Ret_032206_1.CEL.gz 3.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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