NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM994872 Query DataSets for GSM994872
Status Public on Aug 31, 2012
Title MUS_4C.1
Sample type RNA
 
Source name Muscle 4C
Organism Mus musculus
Characteristics strain: C57BL/6J
tissue: skeletal muscle (quadriceps)
treatment: 4 degrees celsius for 4 hours
replicate: 1
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) at 4 degrees celsius for 4 hours 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 -1.456186 0.4574209
ILMN_2721178 1540.497 0
ILMN_2773981 77.37348 0.006082725
ILMN_2771349 76.67273 0.006082725
ILMN_2634566 1474.641 0
ILMN_2737647 21.82102 0.07055961
ILMN_2744574 -5.729375 0.6143552
ILMN_2739275 2.800506 0.3284672
ILMN_2734484 126.1711 0
ILMN_2699078 -9.9884 0.7688565
ILMN_1213681 1236.352 0
ILMN_2735415 32.63448 0.02676399
ILMN_1237980 54.52935 0.01703163
ILMN_3162350 17.20733 0.09854015
ILMN_2712923 140.2661 0
ILMN_2670314 278.2929 0
ILMN_2637698 889.168 0
ILMN_2674228 338.7677 0
ILMN_2438555 1017.503 0
ILMN_2601546 50.69621 0.01703163

Total number of rows: 24607

Table truncated, full table size 724 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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