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Status |
Public on Sep 09, 2020 |
Title |
KYSE510_20 µM SFE-treated cells |
Sample type |
RNA |
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Source name |
KYSE510 with 20 µM SFE treatment
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Organism |
Homo sapiens |
Characteristics |
cell line: KYSE510 cell type: human esophageal cancer cell line treatment: 20 µM Sulforaphene (SFE)
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Treatment protocol |
KYSE510 cells were seeded in 6-well plates with 20 µM SFE treatment or DMSO treatment as the negative control.After cultured for 48h, cells were treated with trizol reagent to extract total RNA.
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Growth protocol |
KYSE510 cells were cultured in RPMI-1640 medium with 10% fetal bovine serum, 100 units/mL penicillin and 100 mg/mL streptomycin.
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Extracted molecule |
total RNA |
Extraction protocol |
Trizol extraction of total RNA was performed according to the manufacturer's instructions.
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Label |
biotin
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Label protocol |
Total RNA was labeled and purified by Affymetrix FL-Ovation™ cDNA Biotin Module V2 according to the manufacturer’s instructions.
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Hybridization protocol |
Following fragmentation, 5.2 µg of biotin-labeled ss-cDNA were hybridized for 16 h at 45℃ on Affymetrix GeneChip Hybridization Oven 645. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
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Scan protocol |
GeneChips were scanned using the Affymetrix GeneChip Scanner 3000 7G.
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Description |
Gene expression data from hunam esophageal cancer KYSE510 cells with 20 µM SFE treatment
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Data processing |
Command Console Software was used to control the scanner and summarize probe cell intensity data (CEL file generation) with default settings. Then raw data were normalized by Expression Console.
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Submission date |
May 19, 2020 |
Last update date |
Sep 09, 2020 |
Contact name |
sichong han |
E-mail(s) |
hansichong@cicams.ac.cn
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Organization name |
beijing university of chemical technology
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Street address |
No. 15 North Third Ring East Road, Chaoyang District
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City |
beijing |
ZIP/Postal code |
100029 |
Country |
China |
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Platform ID |
GPL17586 |
Series (1) |
GSE150891 |
Expression data in EC109 and KYSE510 cells |
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