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Sample GSM2188265 Query DataSets for GSM2188265
Status Public on Mar 08, 2017
Title PANC1_T+VAL_1
Sample type RNA
 
Source name PANC-1, TGF + Valproate treated
Organism Homo sapiens
Characteristics cell line: Panc-1
treatment: TGFb1+NaValproate
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: JP310
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 5.18610111178885
11715101_s_at 7.29596277015177
11715102_x_at 5.3075670855603
11715103_x_at 6.15165333509314
11715104_s_at 6.32455640138952
11715105_at 4.08715190411824
11715106_x_at 6.14485754809548
11715107_s_at 8.39883051138104
11715108_x_at 4.58997440222381
11715109_at 4.98035425513697
11715110_at 6.72831411039355
11715111_s_at 10.0129848541417
11715112_at 4.34981543300791
11715113_x_at 9.34567806899975
11715114_x_at 9.20981710166902
11715115_s_at 3.57196913097126
11715116_s_at 5.5091537917782
11715117_x_at 3.42064390368474
11715118_s_at 4.60907373261787
11715119_s_at 5.42527163591065

Total number of rows: 49193

Table truncated, full table size 1460 Kbytes.




Supplementary file Size Download File type/resource
GSM2188265_hyb19396.CEL.gz 2.2 Mb (ftp)(http) CEL
Processed data included within Sample table

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