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Status |
Public on Oct 27, 2006 |
Title |
HCaRG vs NEO |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by array
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Summary |
Summary: HEK293 cells were transfected with control plasmid (pcDNA1/Neo; Invitrogen) or with the plasmid encoding HCaRG by a standard calcium phosphate co-precipitation method. The clones expressing the highest levels of HCaRG, HCaRG clone 8 and 9 were used in this experiment, while clone transfected with vector alone, Neo clone, served as control. Stable transfectants were synchronized and grown in the presence of 10% FBS for 48 h. Total RNAs were purified with the mini RNeasy kit (Qiagen).
Keywords: parallel sample
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Overall design |
Chips HG-U133 Plus 2.0: - Labeling protocol: GeneChip IVT Labeling Kit. - Hybridization: According to the manufacturer's protocol (Affymetrix). - Scanner: GeneChip Scanner 3000. - Normalization: Employing GCOS software, chips were normalized using all probe sets scaling option and target signal at 500.
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Contributor(s) |
El Hader C, Hamet P, Tremblay J |
Citation(s) |
16033922 |
Submission date |
Apr 28, 2006 |
Last update date |
Mar 25, 2019 |
Contact name |
Johanne Tremblay |
E-mail(s) |
johanne.tremblay@umontreal.ca
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Phone |
514-890-8000-12721
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Organization name |
CHUM Research Center, Hotel-Dieu
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Street address |
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City |
Montreal |
State/province |
QUE |
ZIP/Postal code |
H2W 1T8 |
Country |
Canada |
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Platforms (1) |
GPL570 |
[HG-U133_Plus_2] Affymetrix Human Genome U133 Plus 2.0 Array |
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Samples (8)
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Relations |
BioProject |
PRJNA95675 |