NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM610393 Query DataSets for GSM610393
Status Public on Feb 09, 2012
Title Identification of miR-1 target genes in HNSCC, HSC3
Sample type RNA
 
Channel 1
Source name miR-1 transfected in HNSCC cell line (HSC3)
Organism Homo sapiens
Characteristics cell line: HSC3
cell type: head and neck squamous cell carcinoma
miRNA: miR-1
Treatment protocol microRNA transfection using Lipofectamine RNiMAX (Invitrogen).
Growth protocol Normal cell culture medium RPMI 1640 or MEM.
Extracted molecule total RNA
Extraction protocol Total RNA extracted using Trizol following the manufacturer's instructions.
Label Cy3
Label protocol Agilent two-color Low RNA Input Linear Amplification Kit labeling protocol.
 
Channel 2
Source name control microRNA-transfected cell line (HSC3)
Organism Homo sapiens
Characteristics cell line: HSC3
cell type: head and neck squamous cell carcinoma
miRNA: control
Treatment protocol microRNA transfection using Lipofectamine RNiMAX (Invitrogen).
Growth protocol Normal cell culture medium RPMI 1640 or MEM.
Extracted molecule total RNA
Extraction protocol Total RNA extracted using Trizol following the manufacturer's instructions.
Label Cy5
Label protocol Agilent two-color Low RNA Input Linear Amplification Kit labeling protocol.
 
 
Hybridization protocol Agilent two-color gene expression hyb/wash protocol.
Scan protocol Microarray slides were scanned in an Agilent Technologies G2505B Microarray Scanner at 5 micron resolution. Images were quantified using Agilent Feature Extraction software version 9.5.3.
Description Differentially expressed genes by miR-1 transfection.
Data processing LOWESS-normalized, background-subtracted VALUE data obtained from log10 of processed Red signal/processed Green signal. Agilent Feature Extraction software version 9.5.3 was used.
 
Submission date Oct 18, 2010
Last update date Feb 10, 2012
Contact name Naohiko Seki
E-mail(s) naoseki@faculty.chiba-u.jp
Phone 81-43-226-2971
Fax 81-43-227-3442
Organization name Chiba University
Department School of Medicine
Lab Functional Genomics
Street address 1-8-1 Inohana,Chuo-ku
City Chiba
State/province Chiba
ZIP/Postal code 260-8670
Country Japan
 
Platform ID GPL10332
Series (1)
GSE24782 Identification of target genes of tumor suppressor microRNAs in human cancer

Data table header descriptions
ID_REF
VALUE normalized log10 ratio Cy3/Cy5
INV_VALUE normalized log10 ratio Cy5/Cy3

Data table
ID_REF VALUE INV_VALUE
1 -0.00404353 4.043531014e-003
2 0.000000000e+000 0.000000000e+000
3 0.00881272 -8.812723813e-003
4 0.000000000e+000 0.000000000e+000
5 0.000000000e+000 0.000000000e+000
6 0.000000000e+000 0.000000000e+000
7 0.000000000e+000 0.000000000e+000
8 0.000000000e+000 0.000000000e+000
9 0.000000000e+000 0.000000000e+000
10 0.000000000e+000 0.000000000e+000
11 0.000000000e+000 0.000000000e+000
12 0.544854 -5.448544940e-001
13 -0.014167 1.416697183e-002
14 0.145407 -1.454066052e-001
15 -0.0742137 7.421367688e-002
16 -0.0796241 7.962406824e-002
17 0.230243 -2.302426666e-001
18 -0.0489151 4.891514759e-002
19 0.0655387 -6.553865980e-002
20 0.0628437 -6.284367723e-002

Total number of rows: 44495

Table truncated, full table size 1486 Kbytes.




Supplementary file Size Download File type/resource
GSM610393.txt.gz 15.3 Mb (ftp)(http) TXT
Processed data included within Sample table

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