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Sample GSM722985 Query DataSets for GSM722985
Status Public on Oct 01, 2011
Title Untreated-2
Sample type RNA
 
Source name Chondrocytes in micromass, untreated
Organism Bos taurus
Characteristics cell type: articular chondrocyte micromass
treatment group: Untreated
Treatment protocol After overnight culture, cells were treated with vehicle or with 5ng/ml of TGFß1 (R&D Systems) for 8 hours.
Growth protocol Bovine articular chondrocyte micromass cultures were set up according to the methods of Chen et al., BBRC 1993; Luyten et al., ECR 1994.
Extracted molecule total RNA
Extraction protocol RNA was extracted from the cells in culture using the standard Trizol method. RNA was Dnase treated and then tested using RT-PCR to assure there was no DNA contamination in the samples.
Label biotin
Label protocol Detailed genechip analysis procedures are presented in the Manufacturer’s GeneChip Expression Technical Manual (Affymetrix). Briefly, 50ng of total RNA from each sample was used in a two cycle cDNA amplification protocol using T7-linked oligo dT primers as per the manufacturer’s instructions. After the first round of cDNA synthesis an in vitro transcription step was utilized to amplify the RNA following which a second round of cDNA synthesis was performed. Subsequently, cRNA was generated and biotin was incorporated into the cRNA strand by standard methods (Affymetrix) followed by cRNA fragmentation, and preparation of hybridization cocktail.
 
Hybridization protocol The arrays were hybridized overnight at 45oC, and then washed, stained, and scanned the next day. Detailed genechip analysis procedures are presented in the Manufacturer’s GeneChip Expression Technical Manual (Affymetrix).
Scan protocol Gene expression levels were extracted using AGCC (Affymetrix GeneChip Command Console). Detailed genechip analysis procedures are presented in the Manufacturer’s GeneChip Expression Technical Manual (Affymetrix).
Data processing The data was analyzed with Genesprings using the default settings. The summarized probeset was generated using RMA summarization algorithm. Quantile normalization was used.
 
Submission date May 11, 2011
Last update date Oct 01, 2011
Contact name Rosa Serra
E-mail(s) rserra@uab.edu
Phone 205-934-0842
Organization name University of Alabama at Birmingham
Department Cell Biology
Lab Serra
Street address 1918 University Blvd. 660 MCLM
City Birmingham
State/province AL
ZIP/Postal code 35294-0005
Country USA
 
Platform ID GPL2112
Series (1)
GSE29233 Genes regulated by TGF-beta in bovine articular chondrocytes

Data table header descriptions
ID_REF
VALUE log2 RMA normalized signal

Data table
ID_REF VALUE
AFFX-BioB-5_at -0.15082932
AFFX-BioB-M_at -0.026284218
AFFX-BioB-3_at -0.06262922
AFFX-BioC-5_at -0.01952076
AFFX-BioC-3_at 0.004832268
AFFX-BioDn-5_at -0.026403427
AFFX-BioDn-3_at 0.06014824
AFFX-CreX-5_at -0.03143692
AFFX-CreX-3_at -0.035402298
AFFX-DapX-5_at 0.005849838
AFFX-DapX-M_at -0.17652774
AFFX-DapX-3_at 0.023232222
AFFX-LysX-5_at -0.027014494
AFFX-LysX-M_at -0.04291463
AFFX-LysX-3_at -0.06270194
AFFX-PheX-5_at -0.06630874
AFFX-PheX-M_at 0.10698271
AFFX-PheX-3_at 0.084845066
AFFX-ThrX-5_at 9.82E-04
AFFX-ThrX-M_at 4.34E-04

Total number of rows: 24128

Table truncated, full table size 670 Kbytes.




Supplementary file Size Download File type/resource
GSM722985.CEL.gz 2.0 Mb (ftp)(http) CEL
Processed data included within Sample table

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