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Status |
Public on Jun 16, 2014 |
Title |
SUP-HD1-FOXO1(3A)ER_4OHT_rep1 |
Sample type |
RNA |
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Source name |
SUP-HD1-FOXO1(3A)ER, 4OHT, 24 h
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Organism |
Homo sapiens |
Characteristics |
cell type: cHL cell line cell line: SUP-HD1 treatment: SUP-HD1-FOXO1(3A)ER cells incubated with 4OHT for 24 hours
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Treatment protocol |
KM-H2-KLF4ER and L428-KLF4ER cells were incubated with 200 µM 4-OHT or with relevant amount of the vehicle (ethanol). The experiment was done twice. After 24 h of incubation total RNA was isolated with RNeasy mini kit (QIAGEN).
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Growth protocol |
KM-H2, L428, L1236, UHO-1. and SUP-HD1 cHL cell lines stably expressing FOXO1(3A)ER were grown in RPMI1640 medium with addition of 10% FCS, glutamine and antibiotics at 37 ºC, 5% CO2
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Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was isolated with RNeasy mini kit (QIAGEN) according to the manufacturers instruction.
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Label |
biotin
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Label protocol |
The total RNAs were amplified and labeled following the Whole Transcript (WT) Sense Target Labeling Assay (http://www.affymetrix.com).
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Hybridization protocol |
Labeled ssDNA was hybridized to Human Gene 1.0 ST Affymetrix GeneChip arrays (Affymetrix, Santa Clara, CA).
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Scan protocol |
The chips were scanned with a Affymetrix GeneChip Scanner 3000 according to the Affimetrix protocol.
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Description |
SUP-HD1-FOXO1(3A)ER cells incubated with 4OHT for 24 hours
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Data processing |
The microarray data were processed using GeneSifter software (Perkin Elmers) using RMA normalization protocol.
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Submission date |
Jun 16, 2014 |
Last update date |
Jun 16, 2014 |
Contact name |
Alexey Ushmorov |
E-mail(s) |
[email protected]
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Phone |
+49 (0) 731 50033847
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Organization name |
Ulm University
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Department |
Institute of Physiological Chemistry
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Street address |
Albert-Einstein-Allee 11
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City |
Ulm |
ZIP/Postal code |
89081 |
Country |
Germany |
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Platform ID |
GPL6244 |
Series (1) |
GSE29545 |
Expression data of cHL cell lines after FOXO1 activation |
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