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Sample GSM994871 Query DataSets for GSM994871
Status Public on Aug 31, 2012
Title MUS_RT.2
Sample type RNA
 
Source name Muscle RT
Organism Mus musculus
Characteristics strain: C57BL/6J
tissue: skeletal muscle (quadriceps)
treatment: room temperature (control)
replicate: 2
Treatment protocol Animal studies were performed under approved UCLA animal research protocols and according to guidelines established in the Guide for Care and Use of Laboratory Animals. Mice were maintained in 12-h light/dark conditions and fed a laboratory chow diet that consisted of 4.5% fat, 50% carbohydrate by weight (Lab Diet, Purina 50010). Prior to cold exposure, C57BL/6J mice were provided with food and water ad libitum overnight. On the next morning, the mice were housed without food or bedding and then were placed at 4°C for 4 h. After euthanasia, tissues were collected and frozen until use.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated from mouse tissues by extraction with TRIzol (Invitrogen).
Label biotin
Label protocol Samples were then labeled using standard Illumina protocols (The Southern California Genotyping Consortium at UCLA). Illumina TotalPrep RNA Amplification Kit (Ambion; Austin, TX, cat # IL1791) In short, 0.5g of total RNA was first converted into single-stranded cDNA with reverse transcriptase using an oligo-dT primer containing the T7 RNA polymerase promoter site and then copied to produce double-stranded cDNA molecules. The double stranded cDNA was cleaned and concentrated with the supplied columns and used in an overnight in-vitro transcription reaction where single-stranded RNA (cRNA) was generated and labeled by incorporation of biotin-16-UTP.
 
Hybridization protocol Samples were hybridized to Illumina BeadChips using standard protocols (The Southern California Genotyping Consortium at UCLA). In short, a total of 0.75ug of biotin-labeled cRNA was hybridized at 58 degrees C for 16 hours to Illumina's Sentrix MouseRef-8 Expression BeadChips (Illumina, San Diego, CA). Each BeadChip has 24,000 well-annotated RefSeq transcripts with approximately 30-fold redundancy. The arrays were washed, blocked and the labeled cRNA was detected by staining with streptavidin-Cy3.
Scan protocol Arrays were scanned at a resolution of 0.8um using the Beadstation 500 X from Illumina.
Description Muscle (quadriceps) control at room temperature replicate 2
Data processing The data were normalized using quantile normalization through the beadarray R package.
 
Submission date Aug 30, 2012
Last update date Aug 31, 2012
Contact name Christopher L Plaisier
E-mail(s) [email protected]
Phone 2067322139
Organization name Institute for Systems Biology
Lab Nitin Baliga
Street address 401 Terry Avenue North
City Seattle
State/province Washington
ZIP/Postal code 98109
Country USA
 
Platform ID GPL6103
Series (1)
GSE40486 Zbtb16 Has a Role in Brown Adipocyte Bioenergetics

Data table header descriptions
ID_REF
VALUE quantile normalized
Detection Pval

Data table
ID_REF VALUE Detection Pval
ILMN_1238136 2.176525 0.3454988
ILMN_2721178 1725.585 0
ILMN_2773981 102.2831 0.003649635
ILMN_2771349 93.27682 0.003649635
ILMN_2634566 1700.023 0
ILMN_2737647 32.66633 0.03284672
ILMN_2744574 -4.795846 0.5839416
ILMN_2739275 -3.773637 0.5498784
ILMN_2734484 125.9096 0.00243309
ILMN_2699078 -7.951903 0.7141119
ILMN_1213681 1071.671 0
ILMN_2735415 11.08528 0.1666667
ILMN_1237980 97.60791 0.003649635
ILMN_3162350 25.99126 0.05352798
ILMN_2712923 119.5102 0.003649635
ILMN_2670314 237.7888 0
ILMN_2637698 916.6105 0
ILMN_2674228 429.0298 0
ILMN_2438555 979.1818 0
ILMN_2601546 47.6437 0.02068127

Total number of rows: 24607

Table truncated, full table size 727 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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