|
Status |
Public on Dec 31, 2016 |
Title |
MP1, biological rep1 |
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 |
|