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Sample GSM550719 Query DataSets for GSM550719
Status Public on Jun 07, 2011
Title ALI-D14, donor 2
Sample type RNA
 
Source name Human nasal epithelial cells
Organism Homo sapiens
Characteristics tissue: human nasal mucosa
differentiation step: Onset of mucociliary differentiation
Treatment protocol At confluency (day 7 after seeding), cultures cells were switched in air-liquid interface (ALI) in the differentiating medium.
Growth protocol Dissociated cells from nasal polyps were either seed on collagen-type IV coated permeable supports for differentiation.
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Label Cy3
Label protocol The microRNAs were labled using the miRNA Complete Labeling and Hyb Kit. Details were that 100 ng total RNA was treated with phosphatase at 37 ℃for 30min. The dephosphorylated RNA was ligated and labeled using the ligation master mix following the kit instructions
 
Hybridization protocol Cy3-labeled RNA were hybridized following manufacturer's instructions (MiRNA complete labeling and hybridization kit, Agilent Technologies) 20 hours at 55°C in a rotating Agilent hybridization oven. After hybridization, microarrays were washed 1 minute at room temperature with GE Wash Buffer 1 (Agilent) and 1 minute with 37°C GE Wash buffer 2 (Agilent), then dried immediately by brief centrifugation.
Scan protocol Scanned on an Agilent G2565AA Scanner.
Description MicroRNA expression data
Data processing GeneView files were generated using Agilent's Feature Extraction software version 9.5.3.1
 
Submission date Jun 04, 2010
Last update date Jun 07, 2011
Contact name Kevin Lebrigand
Organization name IPMC/CNRS
Lab Functional Genomics Platform of Nice-Sophia-Antipolis, France.
Street address 660 route des lucioles
City Valbonne - Sophia-Antipolis
ZIP/Postal code 06560
Country France
 
Platform ID GPL8227
Series (2)
GSE22141 MicroRNA signature during the time course of regeneration of the human airway mucociliary epithelium
GSE22147 microRNAs-449 control vertebrate multi-ciliogenesis by repressing Notch signalling

Data table header descriptions
ID_REF
VALUE The values in the matrix are based on the log2(gTotalGeneSignal) column in the GeneView files. For each miRNA, expression values below the noise level (represented by the gTotalGeneError column) were replaced by the log2(gTotalGeneError). All samples were then normalized by quantile method.

Data table
ID_REF VALUE
DarkCorner 1.884935652
NC1_00000197 2.992783471
NC1_00000215 3.091370299
NC2_00079215 3.017998406
NC2_00092197 3.031459557
NC2_00106057 3.06827569
NC2_00122731 3.047764604
NegativeControl 5.142885015
SCorner3 -0.318688526
dmr_285 1.252816077
dmr_3 1.273844457
dmr_308 1.26405075
dmr_316 1.291127207
dmr_31a 1.277150476
dmr_6 1.301447342
ebv-miR-BART1-3p 0.361469843
ebv-miR-BART1-5p 0.357688565
ebv-miR-BART10 0.359108819
ebv-miR-BART10* 0.357199604
ebv-miR-BART11-3p 0.357376415

Total number of rows: 821

Table truncated, full table size 20 Kbytes.




Supplementary file Size Download File type/resource
GSM550719_US84100218_251911812279_S01_miRNA-v1_10_Apr08_1_1.txt.gz 1002.7 Kb (ftp)(http) TXT
Processed data included within Sample table

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