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Sample GSM4767210 Query DataSets for GSM4767210
Status Public on Sep 07, 2021
Title MDA-MB-231 shS100A10_5 rep2
Sample type RNA
 
Source name MDA-MB-231
Organism Homo sapiens
Characteristics tissue: breast cancer
cell line: MDA-MB-231
treatment: S100A10 knock-downed
Treatment protocol none
Growth protocol 10% FBS RPMI1640 + penicillin/streptomycin + 2.5ug/ml puromycin
Extracted molecule total RNA
Extraction protocol total RNA was extracted using PureLink RNA mini kit (ThermoFisher Scientific) according to the manufacturer's instructions.
Label biotin and streptavidin phycoerythrin
Label protocol cDNA samples were labeled with a proprietary DNALabeling Reagent that is covalently linked to biotin using GeneChipTM WT Plus Reagent Kit for Cartridge Array (ThermoFisher Scientific) according to the manufacturer's instructions.
 
Hybridization protocol cDNA was hybridized to Clarion S array (ThermoFisher Scientific) using the GeneChip WT PLUS Reagent Kit and the GeneChip Hybridization, Wash and Stain Kit (ThermoFisher Scientific).
Scan protocol The array chips were scanned immediately after washing with GeneChip Scanner 3000 7G (ThermoFisher Scientific).
Description Gene expression of cell
Data processing Raw data (CEL files) were processed with Transcriptome Analysis Console (TAC) 4.0.2 (TheromoFisher SCIENTIFIC).
The data (21448 probes) were filtered manually as follow. The probes, which showed values lower than the back-round in all samples were excluded (the number became 19605 probes). Then, one probe was selected among probes which detect expression of same gene by original perl script. Briefly, the values of all samples were averaged, and the one which showed highest value was chosen. If the averages were same, the probe which showed lower coefficient of variance (CV) was chosen (the number of probes became 18130 probes). Thereafter the probes which detect multiple genes were omitted (the number of probes became 18130 probes). Finally the probes which showed CV higher than 50% in any conditions were excluded; as a total, mRNA expression of 16965 genes were obtained.
 
Submission date Sep 04, 2020
Last update date Sep 07, 2021
Contact name Nishimura Tatsunori
E-mail(s) [email protected]
Organization name Nagoya University
Department Graduate School of Medicine
Lab Division of Cancer Biology
Street address 65 Tsurumai-cho, Showa-ku
City Nagoya
State/province Aichi
ZIP/Postal code 466-8550
Country Japan
 
Platform ID GPL23159
Series (1)
GSE157497 Gene expression of S100A10 knocked down human breast cancer cells

Data table header descriptions
ID_REF
VALUE Normalized signal

Data table
ID_REF VALUE
TC1200009847.hg.1 9.090061152
TC1200006736.hg.1 14.64229712
TC0100013650.hg.1 13.20552726
TC2200008888.hg.1 74.60446129
TC1200010798.hg.1 2908.500829
TC1200009303.hg.1 298.583369
TC0500013029.hg.1 37.51121271
TC0300009192.hg.1 19.76094451
TC0100006903.hg.1 52.52272997
TC0100006900.hg.1 9.581954747
TC0400012396.hg.1 1159.88013
TC0900010920.hg.1 2625.852202
TC1500009845.hg.1 1475.32798
TC0200012961.hg.1 1193.481096
TC1100008541.hg.1 636.5455746
TC0200015720.hg.1 143.8927406
TC1700008946.hg.1 18.89601356
TC2000007243.hg.1 3092.375934
TC0800008631.hg.1 104.5703474
TC1600010752.hg.1 4983.936597

Total number of rows: 16965

Table truncated, full table size 495 Kbytes.




Supplementary file Size Download File type/resource
GSM4767210_2020-7-27-6_Clariom_S_Human.CEL.gz 1.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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