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Sample GSM881304 Query DataSets for GSM881304
Status Public on Dec 31, 2016
Title MP1, biological rep2
Sample type RNA
 
Source name SCC172, MP1 fraction
Organism Homo sapiens
Characteristics cell line: SCC172
fraction: MP1
cell type: oral squamous cell carcinoma (OSCC) cells
Treatment protocol Side population analysis was based on the previously described method (Goodell et al., 1997) with slight modifications. Briefly, cells were incubated (1x10^6cells/ml) in pre-warmed DMEM supplemented with 2% fetal bovine serum (FBS) (Sigma) and 10Mm HEPES (Sigma) containing 5 µg/ml Hoechst 33342 for 45 minutes at 37C (water-bath) with intermittent mixing. After incubation, stained cells were washed and re-suspended in ice-cold HBSS (Sigma) supplemented with 2% FBS. Propidium iodide (1µg/ml) was added immediately before analysis to label dead cells. Analysis and sorting was performed on FACS Aria II (BD Biosciences) using Diva Software.
Growth protocol The OSCC cell line SCC172 were adherent cells maintained in Dulbecco’s Modified Eagle’s Medium (Sigma, D1152) containing 25mM HEPES and 3.6g/L sodium bicarbonate supplemented with 10% Foetal Bovine Serum (FBS, Sigma) and 1% antibiotic antimycotic cocktail (Invitrogen). Cells were incubated at 37C with 5% CO2 in a humidified incubator.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated using Qiagen’s All Prep DNA/RNA Mini Kit (Cat. No. 80204) following the manufacturer’s instructions.
Label Biotin
Label protocol 100ng of total RNA were used for preparation of biotin-labeled targets (cRNA) using modified MessageAmp™ -based protocols (Ambion Inc., Austin, TX).
 
Hybridization protocol Labeled cRNA was fragmented in a 0.5ug/uL reaction and used for array hybridization and washing according to the standard Affymetrix protocol on an Affymetrix FS450 Fluidics station.
Scan protocol The arrays were scanned on an Affymetrix GeneChip Scanner 3000 7G using the Affymetrix Statistical Algorithm MAS 5.0 (GCOS v1.3) algorithm.
Description Differential expression analysis of genes in MP1.
Data processing Softwares used for analysis were Partek Genomic Solutions 6.2 (Partek Inc., St. Charles, MO), Matlab 7 (Mathworks Inc., MA) and GCOS 1.3 (Affymetrix Inc., CA).
 
Submission date Feb 27, 2012
Last update date Dec 31, 2016
Contact name Vinitha Richard
E-mail(s) [email protected]
Phone +91 9972844405
Organization name Rajiv Gandhi Centre for Biotechnology
Department Cancer Research Program
Lab MRP Lab
Street address Thycaud P.O.
City Thiruvananthapuram
State/province Kerala
ZIP/Postal code 695014
Country India
 
Platform ID GPL571
Series (1)
GSE36111 Expression data from side population cells of the human OSCC cell line SCC172

Data table header descriptions
ID_REF
VALUE MAS5.0 signal intensity (value set to 500)

Data table
ID_REF VALUE
205749_at 6.613236955
213418_at 6.749534268
203603_s_at -1
1405_i_at 0.137503524
216598_s_at 1.584962501
219274_at 2.232660757
117_at 5.501439145
211741_x_at 1.632268215
213800_at 4.432959407
205476_at 3.916476644
205893_at -1.736965594
206931_at 3.608809243
204698_at 3.95419631
207284_s_at 4.44625623
217262_s_at 1.963474124
206175_x_at 2.432959407
208257_x_at 2.070389328
216874_at -0.736965594
212768_s_at 1.070389328
203708_at 1.321928095

Total number of rows: 22277

Table truncated, full table size 494 Kbytes.




Supplementary file Size Download File type/resource
GSM881304_H0029314.CEL.gz 2.0 Mb (ftp)(http) CEL
Processed data included within Sample table
Processed data are available on Series record

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