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Sample GSM236895 Query DataSets for GSM236895
Status Public on Jun 10, 2008
Title RT4 cells grown on Plastic, replicate 2; Matrigel next
Sample type RNA
 
Source name RT4 papilloma cell line
Organism Homo sapiens
Characteristics RT4 cell line is a urinary bladder transitional cell papilloma cell line from the American Type Culture Collection, Manassas Virginia
Biomaterial provider American Type Culture Collection, Manassas Virginia
Treatment protocol Three dimensional gel cultures with Matrigel were performed by layering 0.8 mls of ice cold Matrigel onto polyethylene terephthalate membranes of 6-well cell culture inserts (Falcon, Becton-Dickinson Labware, Franklin Lakes, NJ). Gels were solidified at 37º C.
RT4 cells were trypsinized, brought up on 20 mls McCoys media with 10% Fetal Calf Serum (FCS). Cells were centrifuged then brought up in McCoys media with 10% FCS to a concentration of 500,000 cells/250µl. 250µl added on top of each solidified matrigel disc and 2mls of McCoys with 10% FCS layered underneath each culture insert
Growth protocol Cells were maintained for 10 days and media replenished underneath the insert twice a week. Cells were harvested at 12 hrs, 24hrs, 2 days, 3 days, 4days, 6 days, 7 days, 8 days, and 9 days of growth in culture using Matrisperse (Falcon, Becton-Dickinson Labware, Franklin Lakes, NJ) and RNA collected
Extracted molecule total RNA
Extraction protocol RNA was isolated at each time point with RNAeasy kit (QIAGEN Inc.,Valencia, CA) according to manufacturer’s protocol
Label Cy3
Label protocol Omniscript reverse-transcriptase, 37 C, 2 hrs
 
Hybridization protocol Ventana Discovery 9h, 58 C washed to 0.1xSSC
Scan protocol scanned on Agilient G2505B scanner Imagene 5.0
Description Details about microarray handling/processing techniques can be obtained from platform’s manufacturer
Data processing Data were normalized as was described previously in Dozmorov I et al., Nucleic Acids Res. 2004 Oct 28;32(19). In general, intensities were converted to expression and normalized to low-expressed genes, which provide possible technical noise level. The arrays are then adjusted to each other by robust linear regression and this Log10 transformed data presented for each sample. Group of low-expressed genes is selected by normal distribution fitting. This group provides internal standard of measurement noise (ISMN). Genes above 5SD from mean of ISMN were selected as expressed
 
Submission date Oct 10, 2007
Last update date Aug 14, 2011
Contact name Robert Evan Hurst
E-mail(s) robert-hurst@ouhsc.edu
Phone 405-271-3930
Fax 405-271-3289
Organization name Oklahoma University Health Sciences Center
Department Urology
Lab Adult Urology Lab
Street address 920 S. L. Young Blvd
City Oklahoma City
State/province OK
ZIP/Postal code 73112
Country USA
 
Platform ID GPL3463
Series (1)
GSE9291 Systems biology of gene expression of bladder papilloma cells modulated by a malignant-derived extracellular matrix

Data table header descriptions
ID_REF
VALUE Normalization & Linear regression applied, Log10 values
VALUE_RAW Non-treated raw data

Data table
ID_REF VALUE VALUE_RAW
005001017018 1.223081771 100
006001014022 1.750958464 579.8
006004013022 0.493569055 10.1
003002012018 1.63288557 390.7
004003015010 1.74748397 573.1
008003019009 1.745390174 569.1
001002016001 1.506918518 256.6
001001008009 1.015892551 50.7
007003009026 1.485725464 239.1
001004014009 -2.385181353 -48.4
003004005019 0.745310032 21.4
002001013017 1.322810061 139.1
006003017019 1.336991679 145.8
005001003012 1.590828036 339.5
004004004007 1.695719905 482
005004002014 1.12748434 73
005002008014 1.64275655 403.8
005002006022 1.424650212 195.1
004001003011 1.782717191 644.8
002004001026 0.899289078 34.8

Total number of rows: 22464

Table truncated, full table size 668 Kbytes.




Supplementary file Size Download File type/resource
GSM236895_RAW.txt.gz 103.9 Kb (ftp)(http) TXT
Processed data included within Sample table

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