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Sample GSM129296 Query DataSets for GSM129296
Status Public on Sep 24, 2006
Title Profiling of altered gene expression induced by 1 hr of zinc in human prostate cells
Sample type RNA
 
Source name Human prostatic cell line derived from normal prostate epithelial tissue (HPR-1)
Organism Homo sapiens
Characteristics HPR-1
Biomaterial provider Dr. C.K. Choo, University of Hong Kong, China
Treatment protocol Zinc effect was initiated with cells at 70-80% confluence in T-75 flasks (Corning, Corning, NY) which were synchronized by 24 hrs hormone-depletion before the introduction of zinc treatments. Hormone-free media were refreshed following starving process and zinc (1,500 ng /mL) was introduced for 1 hr. Both media and Cells from various treatments were collected concurrently. Pellets were immediately frozen and stored at -80 oC pending for RNA isolation.
Growth protocol Cells were maintained and propagated in Keratinocyte-SFM supplemented with 1U/mL penicillin and streptomycin sulfate, EGF 0.005 mg/mL, and bovine pituitary extract 0.05 mg/mL in a 5% CO2 atmosphere at 37oC.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted with the Qiagen (Valencia, CA) RNeasy Mini kit according to the manufacturer’s protocol.
Label Chemiluminescent Fluorescence
Label protocol Applied Biosystems Protocol
 
Hybridization protocol Applied Biosystems Protocol
Scan protocol Applied Biosystems Protocol
Description Zinc effect on gene expression of HPR-1 cells was evaluated using Applied Biosystems (Foster City, CA) human genomewise microarray chips V2.0. For each chip, 2µg total RNA from each sample was used for converting to cRNA. The synthesis of cRNA and a subsequent hybridization were completed by the Core Facility at UMBI (University of Maryland Biotechnology Institute, Baltimore, MD) according to the ABI standard protocol.
Data processing Applied Biosystems 1700 Chemiluminescent Microarray Analyzer and 1700 Gene Expression Microarray System
 
Submission date Aug 18, 2006
Last update date Aug 24, 2006
Contact name Shufei Lin
E-mail(s) slin@umaryland.edu
Phone 410-706-7340
Fax 410-706-7340
Organization name University of Maryland at Baltimore
Department Biomedical Sciences
Lab 4D-08 Dental School
Street address 666 W. Baltimore Street
City Baltimore
State/province MD
ZIP/Postal code 21201
Country USA
 
Platform ID GPL2986
Series (1)
GSE5590 Profiling of zinc altered gene expression in human prostate normal (HPR-1) and malignant (PC-3) cells

Data table header descriptions
ID_REF
Signal_HPR1-1hrZn Raw signal count data
VALUE same as UNF_VALUE but with flagged values removed
SDEV_HPR1-1hrZn Standard deviation of signal count data
Flag Number other than 0 represents unreliable count data
UNF_VALUE Normalized (scaled) signal count data (not log transformed)

Data table
ID_REF Signal_HPR1-1hrZn VALUE SDEV_HPR1-1hrZn Flag UNF_VALUE
100002 203322.08 57.63 3528.08 0 57.63
100003 238.75 238.75 1 -1.03
100027 256.68 256.68 1 0.64
100036 28975.89 38.01 762.41 0 38.01
100037 32939.75 32.14 1024.77 0 32.14
100039 5069.29 8.43 601.3 0 8.43
100044 345.51 345.51 1 -1.24
100045 920.29 920.29 1 -1.45
100051 309.24 309.24 1 -0.03
100052 609.51 2.14 285.36 0 2.14
100057 4944.94 6.45 766.76 0 6.45
100058 131836.24 62.42 2112.03 0 62.42
100060 1325.45 2.09 635.22 0 2.09
100062 1196 1196 1 0.36
100064 301242.87 66 4564.43 0 66
100079 179110.11 37.76 4743.8 0 37.76
100089 34781.63 35.7 974.41 0 35.7
100093 34462.88 73.84 466.72 0 73.84
100095 850.04 850.04 1 -0.85
100100 78009.18 36.48 2138.26 0 36.48

Total number of rows: 32878

Table truncated, full table size 1075 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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