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Sample GSM79015 Query DataSets for GSM79015
Status Public on Jan 01, 2006
Title fibroblast_skin_stimulated_chipB_rep1
Sample type RNA
 
Source name fibroblast_skin_stimulated
Organism Mus musculus
Characteristics Primary fibroblast, fetal mouse skin, mechanically stimulated
Treatment protocol Embryos used for fibroblast isolation were obtained from a time mated CD1 mouse. At 19-days post conception, the pregnant mouse was euthanized by CO2 asphyxiation and immediately swabbed with 70% ethanol in a sterile hood. Tendon, corneal and skin fibroblasts were isolated according to Spector et al {Spector, Goldman Robert D, et al. 1998 381 /id}. Cells were maintained in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 15% FCS in a 5% CO2 humidified atmosphere at 37 °C, and were subcultured when they reached approximately 80% confluence. Cells were cultured until five population doublings, at which point they were seeded onto a gelatin-coated (1% w/v) glass plate (7cm x 10cm) and allowed to adhere for approximately seven hours prior to stimulation. STIMULATION: Fluid flow was applied to cells using a parallel plate flow chamber described previously {Ohtsuka, Ando, et al. 1993 341 /id}. Wall shear stress (tw) was calculated according to the equation tw = 6mQ/(bh2), where m is the fluid viscosity (0.001 Pa s), Q is the fluid flow rate (ml/s), and b and h are the width (5.5 cm) and height (0.04 cm) of the flow channel, respectively. The assembled system was maintained at 37 °C in a 5% CO2 humidified incubator. In this study, tendon, corneal and skin fibroblasts were subjected to a shear stress of 0.1 dynes/cm2 for 14 hours, with a flow perfusate of DMEM supplemented with 2% FCS and 1% penicillin/streptomycin.
Extracted molecule total RNA
Extraction protocol RNA extractions were carried out with the Absolutely RNA RT-PCR Miniprep kit (Stratagene, La Jolla, CA, USA) according to the manufacturer's instructions. Contaminating RNases were inactivated in solutions upon treatment with 0.1% (v/v) DEPC, while RNaseZap was used according to the manufacturer's instructions to eliminate RNase contamination on work surfaces and pipettes.
Label biotin
Label protocol Standard Affymetrix GeneChip Eukaryotic Two-Cycle Target Labeling
 
Hybridization protocol standard Affymetrix procedures
Scan protocol standard Affymetrix procedures
Description Primary fibroblast from the skin of the fetal mouse, mechanically stimulated by fluid flow
Data processing Robust Multichip Average (RMA, module Affy 1.4.32 of Bioconductor)
 
Submission date Oct 20, 2005
Last update date Oct 20, 2005
Contact name Steve Winder
E-mail(s) s.winder@sheffield.ac.uk
Phone +44 114 222 2332
Fax +44 114 276 5413
URL http://www.shef.ac.uk/bms/research/winder
Organization name University of Sheffield
Department Department of Biomedical Science
Street address Western Bank
City Sheffield
ZIP/Postal code S10 2TN
Country United Kingdom
 
Platform ID GPL340
Series (1)
GSE3486 Mechanically stimulated fibroblast from different fetal mouse tissues using Affy MOE430 chip set

Data table header descriptions
ID_REF
VALUE RMA (v.1.4.32) calculated log2(signal) values

Data table
ID_REF VALUE
1415670_at 10.31683667
1415671_at 11.77660028
1415672_at 11.64779303
1415673_at 9.215685463
1415674_a_at 10.42773038
1415675_at 10.08728018
1415676_a_at 12.44039727
1415677_at 9.140852503
1415678_at 10.49461012
1415679_at 11.69573403
1415680_at 9.158920211
1415681_at 9.743653323
1415682_at 8.113642279
1415683_at 12.01558424
1415684_at 7.706787461
1415685_at 7.492234984
1415686_at 10.5361309
1415687_a_at 11.56354066
1415688_at 10.80677644
1415689_s_at 10.21172152

Total number of rows: 22575

Table truncated, full table size 509 Kbytes.




Supplementary file Size Download File type/resource
GSM79015.CEL.gz 3.3 Mb (ftp)(http) CEL
GSM79015.EXP.gz 521 b (ftp)(http) EXP

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