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Sample GSM2759999 Query DataSets for GSM2759999
Status Public on Aug 28, 2020
Title RecCFPm_Control RecCtrl_rep3
Sample type RNA
 
Channel 1
Source name Inducible MCF7 RecCFPm cancer cell line
Organism Homo sapiens
Characteristics cell line: MCF7
treatment: Induced for 48h with doxycycline
phenotype: RecCFPm
Growth protocol Recombinant RecCtrl, RecCFP and RecCFPm breast cancer cell lines were cultivated under optimal growth conditions and gene expression was induced with 50ng/ml doxycycline for 48 h; a cell pellet was harvested and total RNA was purified according to the extract protocol
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using the mirVana™ miRNA Isolation Kit with phenol from Ambion™ (AM1561, Life technologies) following manufacturer's instructions. NanoDrop Spectrophotometer (NanoDrop Technologies) was used for RNA quantification. The quality of extracted RNA was assessed with Bioanalyzer 2100 (Agilent Technologies) using the RNA 6000 Nano Kit (Agilent Technologies).
Label Cy3
Label protocol 1 µg of total RNA were treated with a Spike-In control (5188-5279, Agilent technologies); cDNA synthesis, cRNA synthesis/amplification and cRNA purification was conducted according to the manufacturer`s instructions: Two-Color Microarray-Based Gene Expression Analysis for Low Input Quick Amp Labeling (5190-2306, Agilent technologies)
 
Channel 2
Source name Inducible MCF7 RecCtrl cancer cell line
Organism Homo sapiens
Characteristics cell line: MCF7
treatment: Induced for 48h with doxycycline
phenotype: RecCtrl
Growth protocol Recombinant RecCtrl, RecCFP and RecCFPm breast cancer cell lines were cultivated under optimal growth conditions and gene expression was induced with 50ng/ml doxycycline for 48 h; a cell pellet was harvested and total RNA was purified according to the extract protocol
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using the mirVana™ miRNA Isolation Kit with phenol from Ambion™ (AM1561, Life technologies) following manufacturer's instructions. NanoDrop Spectrophotometer (NanoDrop Technologies) was used for RNA quantification. The quality of extracted RNA was assessed with Bioanalyzer 2100 (Agilent Technologies) using the RNA 6000 Nano Kit (Agilent Technologies).
Label Cy5
Label protocol 1 µg of total RNA were treated with a Spike-In control (5188-5279, Agilent technologies); cDNA synthesis, cRNA synthesis/amplification and cRNA purification was conducted according to the manufacturer`s instructions: Two-Color Microarray-Based Gene Expression Analysis for Low Input Quick Amp Labeling (5190-2306, Agilent technologies)
 
 
Hybridization protocol The hybridization was conducted with the Hybridization Gasket Slide Kit (G2534-60014, Agilent technologies) and the Gene Expression Hybridization Kit (5188-5242, Agilent technologies) following the manufacturer’s instructions and the samples were hybridized on the SurePrint G3 Custom Gene Expression Microarray 8x60K (G4102A, Agilent technologies)
Scan protocol SurePrint G3 Custom Gene Expression Microarray, 8x60K (G4102A, Agilent Technologies) was scanned in the Agilent 2505C DNA Microarray Scanner with Sure-Scan High Resolution Technology. Images were quantified using Agilent Feature Extraction Software version 10.7.3.1.
Description Biological replicate 3 of 4. Control RecCtrl with empty vector plasmid; RecCFPm
Data processing Raw data were processed using the limma R package. Background normalization was performed using normexp with an offset of 50. Each slide was normalized using LOESS. Between array quantile normalization was performed last.
Quantile (between arrays) and loess (within arrays) normalized M values.
 
Submission date Aug 30, 2017
Last update date Aug 28, 2020
Contact name Ines Block
Organization name Odense University Hospital
Department Department of Clinical Genetics
Street address J.B. Winsløws Vej 4
City Odense
ZIP/Postal code 5000
Country Denmark
 
Platform ID GPL13607
Series (1)
GSE103302 Stable recombinant MCF7 human breast cancer cell lines with inducible expression of CFP (NM_002621.2, RecCFP) or a mutated CFP variant (S27X, RecCFPm) vs. recombinant MCF7 control recombinants expressing an empty expression vector (RecCtrl)

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

Data table
ID_REF VALUE
1 -2.177038232e-002
2 0.000000000e+000
3 0.000000000e+000
4 -7.406945581e-002
5 4.616398786e-003
6 6.882834987e-002
7 6.582269093e-002
8 -4.680575690e-003
9 0.000000000e+000
10 -7.500404558e-002
11 0.000000000e+000
12 -9.445886462e-002
13 -2.418058829e-002
14 -9.884219694e-002
15 9.442254597e-002
16 0.000000000e+000
17 4.613429796e-002
18 0.000000000e+000
19 0.000000000e+000
20 -8.580973333e-003

Total number of rows: 62976

Table truncated, full table size 1429 Kbytes.




Supplementary file Size Download File type/resource
GSM2759999_US84603592_252800421906_S01_GE2_107_Sep09_2_1_3.txt.gz 6.0 Mb (ftp)(http) TXT
Processed data included within Sample table
Processed data provided as supplementary file
Processed data are available on Series record

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