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Status |
Public on Sep 01, 2016 |
Title |
LNCaP transiently overexpressing HIP1- replicate 4 |
Sample type |
RNA |
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Source name |
LNCaP cell line transiently overexpressing HIP1- Day 4 post transfection
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Organism |
Homo sapiens |
Characteristics |
cell type: LNCaP prostate cancer cell line
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Growth protocol |
PNT1a and LNCaP cells were cultured in RPMI supplemented with 10% FBS. PNT1a stable lines were maintained in 0.8 mg/ml G418 supplemented Media.
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Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted using the QIAGEN RNeasy mini kit in accordance with the prescribed protocol provided with the kit. Quality control was performed with Agilent Bioanalyser.
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Label |
biotin
|
Label protocol |
Biotinylated cRNA were prepared with the Ambion MessageAmp kit for Illumina arrays
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Hybridization protocol |
Standard Illumina hybridization protocol
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Scan protocol |
Standard Illumina scanning protocol
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Description |
Replicate 4
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Data processing |
The bead-level data were preprocessed using BASH (Cairns et al. (2008) Bioinformatics 24(24):2921-2), a function from the beadarray package (Dunning et al (2007) Bioinformatics 23(16):2183-4) in Bioconductor, and also log base 2 transformed and quantile normalised using the beadarray package.
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Submission date |
Jan 19, 2012 |
Last update date |
Sep 01, 2016 |
Contact name |
Roslin Russell |
E-mail(s) |
roslin.russell@cruk.cam.ac.uk
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Phone |
01223 769770
|
Organization name |
Cambridge Research Institute, Cancer Research UK
|
Street address |
Robinson Way
|
City |
Cambridge |
ZIP/Postal code |
CB2 0RE |
Country |
United Kingdom |
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|
Platform ID |
GPL6947 |
Series (1) |
GSE35211 |
HIP1 mediates prostate carcinogenesis and progression through STAT3 signalling |
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