NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM3616203 Query DataSets for GSM3616203
Status Public on Jul 01, 2019
Title C4-2-RT_MTH045F04F01_01, biological rep3
Sample type RNA
 
Source name C4-2-N3-RT_MTH045F04F01_01
Organism Homo sapiens
Characteristics cell line: C4-2 (hormone-resistant PCa cells)
tissue: prostate
protocol: tRNA extracted 4h after radiation
Treatment protocol LNCaP and C4-2 cells maintained in 6 well plates for 24 hours. After 24 hours the cells were treated with either 10 uM Enzalutamide (celleckchem) or ADT (charcopl phenol free media) or the combination of both, 2 hours later, the cells were radiated (4Gy). 4 hours after radiation, tRNA was extracted
Growth protocol LNCaP and C4-2 cells are cultured in RPMI media containing 10%FBS
Extracted molecule total RNA
Extraction protocol The toal RNA was isolated by the Rneasy Mini Kit (Qiagen) according to the manufactures' instructions.
Label biotin
Label protocol Total RNA was quantified using a NanoDrop Spectrophotometer ND-1000 (NanoDrop Technologies, Inc.) and its integrity was assessed using a 2100 Bioanalyzer (Agilent Technologies). Sense-strand cDNA was synthesized from 100 ng of total RNA, and fragmentation and labeling were performed to produce ss-cDNA with the GeneChip® WT Terminal Labeling Kit according to manufacturer’s instructions (Thermo Fisher Scientific).
 
Hybridization protocol After fragmentation and labeling, 2.8 µg DNA target was hybridized on Clariom™S HT, Human (Thermo Fisher Scientific) and process on the GeneTitan® Instrument (Thermo Fisher Scientific) for Hyb-Wash-Scan automated workflow. For hybridization on the Gene Titan we use the GeneTitan™ Hybridization, Wash, and Stain Kit for WT Array Plates.
Scan protocol The imaging device in GeneTitan MC Instrument uses an external, high-intensity xenon lamp and dual excitation and emission filters to capture images from array plates for use in expression.
Description tRNA extracted 4h after radiation
Data processing The primary analysis was completed using the R/Bioconductor package. The data was normalized using the 'rma' method in the bioconductor package 'oligo'.
 
Submission date Feb 21, 2019
Last update date Jul 01, 2019
Contact name Thierry Muanza
Organization name McGill Univeristy
Street address 3755 Chemin de la Côte-Sainte-Catherine,
City Montreal
ZIP/Postal code H3T 1E2
Country Canada
 
Platform ID GPL24324
Series (1)
GSE126881 Identification of Radiosensitivity Gene Signatures Induced by Enzalutamide in Prostate cancer cells

Data table header descriptions
ID_REF
VALUE The expression values are transformed to the log2 scale.

Data table
ID_REF VALUE
23064070 9.319473118
23064071 9.099817617
23064072 4.558286177
23064073 9.560879322
23064074 4.370198614
23064075 10.68831735
23064076 7.420982363
23064077 10.21887215
23064078 9.590497768
23064079 5.275492886
23064080 3.334365224
23064081 3.666797907
23064083 5.281335359
23064084 2.930127562
23064085 4.993601304
23064086 3.573695763
23064087 5.012837678
23064088 4.488278309
23064089 3.933303413
23064090 5.656598219

Total number of rows: 27189

Table truncated, full table size 792 Kbytes.




Supplementary file Size Download File type/resource
GSM3616203_C4-2-N3-RT_MTH045F04F01_01.CEL.gz 1.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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