NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM2188275 Query DataSets for GSM2188275
Status Public on Mar 08, 2017
Title PANC1_T_4
Sample type RNA
 
Source name PANC-1, TGF treated
Organism Homo sapiens
Characteristics cell line: Panc-1
treatment: TGFb1
Biomaterial provider ATCC
Treatment protocol EMT was induced by transforming growth factor-β1 (TGF-β1, R&D systems). Cells were first starved for 24 hours in 1% fetal calf serum medium to avoid interference of growth factors in the serum and then stimulated with TGF-β1 (5 ng/ml) or vehicle for 48 hours. For EMT inhibition in Panc-1 cells, acriflavine (2.5 µM, Sigma-Aldrich) or Valproate (Sodium Valproate 2 mM, Sigma-Aldrich) was added to the cell culture together with TGF-β1 for 48h.
Growth protocol Panc-1 pancreatic cancer cells were obtained from ATCC (Rockville, MD, USA) and cultured in Gibco Modified Eagles Medium (Life Technologies) supplemented with 10% fetal calf serum, 2 mM L-glutamine, 100 U/ml Penicillin and 100 µg/ml Streptomycin.
Extracted molecule total RNA
Extraction protocol Rneasy kit (Qiagen)
Label biotin
Label protocol RNA concentration and purity were determined spectrophotometrically using the Nanodrop ND-1000 (Nanodrop Technologies) and RNA integrity was assessed using a Bioanalyser 2100 (Agilent). Per sample, an amount of 200 ng of total RNA spiked with bacterial RNA transcript positive controls (Affymetrix) was amplified and labeled using the GeneChip 3' IVT PLUS kit (Affymetrix). All steps were carried out according to the manufacturers protocol (Affymetrix).
 
Hybridization protocol A mixture of purified and fragmented biotinylated aRNA and hybridisation controls (Affymetrix) was hybridised on Affymetrix' Primeview Human Gene Expression arrays followed by staining and washing in a GeneChip® fluidics station 450 (Affymetrix) according to the manufacturer’s procedures.
Scan protocol To assess the raw probe signal intensities, chips were scanned using a GeneChip® scanner 3000 (Affymetrix).
Description Internal Sample ID: JP316
Data processing Data were normalized using RMA as implemented in the Affy package (version 1.44.0) of Bioconductor. Expression values are represented on a log2-scale.
 
Submission date Jun 06, 2016
Last update date Mar 08, 2017
Contact name Rekin's Janky
E-mail(s) Nucleomics.Bioinformatics@vib.be
Organization name VIB
Department Nucleomics Core
Street address Herestraat 49 Box 816
City Leuven
ZIP/Postal code B-3000
Country Belgium
 
Platform ID GPL15207
Series (2)
GSE82293 Acriflavine inhibits the epithelial-to-mesenchymal transition in vitro in liver and pancreatic cancer cells (part of study with TGF-b1 stimulation)
GSE82299 Acriflavine inhibits the epithelial-to-mesenchymal transition in vitro in liver and pancreatic cancer cells

Data table header descriptions
ID_REF
VALUE Data were normalized using RMA as implemented in the Affy package (version 1.44.0) of Bioconductor. Expression values are represented on a log2-scale.

Data table
ID_REF VALUE
11715100_at 5.00952166663056
11715101_s_at 7.1219752200116
11715102_x_at 5.41256665590797
11715103_x_at 6.15194953565148
11715104_s_at 6.18215927631559
11715105_at 4.20617868690116
11715106_x_at 5.93241209701385
11715107_s_at 8.18705622782845
11715108_x_at 4.39770681943912
11715109_at 4.92715582893929
11715110_at 6.71688337173109
11715111_s_at 9.48027020645942
11715112_at 4.31245868487465
11715113_x_at 8.75242991047078
11715114_x_at 8.5998303594715
11715115_s_at 3.54395657515908
11715116_s_at 5.73201345789903
11715117_x_at 3.39347287166781
11715118_s_at 4.85857795171357
11715119_s_at 5.62389786766688

Total number of rows: 49193

Table truncated, full table size 1460 Kbytes.




Supplementary file Size Download File type/resource
GSM2188275_hyb19634.CEL.gz 2.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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