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Status |
Public on Sep 01, 2013 |
Title |
siLRH-1_#2_rep_1 |
Sample type |
RNA |
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Source name |
MCF-7 human cell line, siLRH-1_#2
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Organism |
Homo sapiens |
Characteristics |
cell line: MCF-7 sirna knockdown: siLRH-1_#2
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Treatment protocol |
Cells were transfected with double-stranded RNA oligonucleotides using the Lipofectamine RNAiMax reverse transfection method (Invitrogen, UK), according to manufacturer's protocols. Two different siRNAs against LRH-1 were used: ON-TARGETplus siRNA J-003430-07 (siLRH-1_#2) and J-003430-08 (siLRH-1_#3) from Dharmacon. siGENOME Non-targeting siRNA (Dharmacon, cat. no.:D-001210-01) (siControl) was used as negative control. All siRNA experiments used the double-stranded RNA oligonucleotides at a final concentration of 80 nM.
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Growth protocol |
MCF-7 cells were cultured in DMEM containing 10% FCS.
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Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted using the RNeasy Kit from QIAGEN following manufacturer's instructions.
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Label |
Biotin
|
Label protocol |
Biotinylated cRNA were prepared with the Ambion Illumina® TotalPrep™-96 RNA Amplification Kit for Illumina arrays.
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Hybridization protocol |
Labelled cRNA was hybridised to the Illumina HumanHT-12 V3.0 expression BeadChip according to the Illumina Whole-Genome Gene Expression Direct Hybridization Assay Guide.
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Scan protocol |
BeadChips were scanned using the BeadArray reader.
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Description |
SAMPLE 5 Replicate 1 of 4.
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Data processing |
The BeadChiP image data were preprocessed using GenomeStudio (Illumina). The expression data were then log2 transformed and quantile-normalised using Partek Genomics Suite.
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Submission date |
Jun 10, 2013 |
Last update date |
Sep 01, 2013 |
Contact name |
Simak Ali |
E-mail(s) |
simak.ali@imperial.ac.uk
|
Organization name |
Imperial College London
|
Department |
Department of Surgery & Cancer
|
Street address |
Du Cane Road
|
City |
London |
ZIP/Postal code |
W12 0NN |
Country |
United Kingdom |
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|
Platform ID |
GPL6947 |
Series (1) |
GSE47803 |
Co-regulated gene expression by estrogen receptor-α and liver receptor homolog-1 is a feature of the estrogen response in breast cancer cells |
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