NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM2283461 Query DataSets for GSM2283461
Status Public on Apr 19, 2017
Title Patient F3434
Sample type RNA
 
Source name Orbicularis Oris Muscle Mesenchymal Stem Cells Primary Cultures (OOMMSC)
Organism Homo sapiens
Characteristics tissue: Orbicularis Oris Muscle
gender: Female
phenotype: Nonsyndromic cleft lip/palate (NSCL/P)
Growth protocol We established OOMMSC primary cultures according to previously published protocol [Bueno et al. 2009] and expanded to 70-90% confluence. We confirmed the mesenchymal immunophenotype of a representative sample of cell cultures through flow cytometry analysis with fluorescent antibodies for markers CD29 (adhesion), CD31 (endothelial), CD45 (hematopoietic), CD73 or CD166, CD90, and CD105 (mesenchymal).
Extracted molecule total RNA
Extraction protocol Total RNA isolation was performed with NucleoSpin RNA II kit (Macherey-Nagel), following manufacturer’s recommendations. RNA quality and concentration were assessed using Nanodrop 1000 and agarose gel electrophoresis. Only RNA samples with absorbance ratio 260/280 > 1.8, preserved rRNA ratio (28S/18S) and no signs of degradation were used.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
 
Hybridization protocol Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip®Human Gene 1.0 ST Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450 and hybridized for 16 hr in the Affymetrix Hybridization Oven 640.
Scan protocol GeneChips were scanned using the Affymetrix GeneChip Scanner 3000 7G
Description Gene expression data from mesenchymal stem cells derived from OOM.
Data processing Data were analyzed with Expression Console (Affymetrix) and normalized by RMA method. We excluded from the expression data the Affymetrix controls and probe sets classified as ‘rescue->FLmRNA->unmapped’ (poorly aligning to transcriptome, Homo sapiens NetAffx annotation release 32, 2011-06-21), also removing probe sets with cross hybridization potential.
 
Submission date Aug 17, 2016
Last update date Apr 19, 2017
Contact name Cibele Masotti
Organization name University of Sao Paulo
Department Genetics and Evolutionary Biology
Lab Human Development Genetics Lab
Street address Rua do Matao, 277.
City Sao Paulo
State/province São Paulo
ZIP/Postal code 05508-090
Country Brazil
 
Platform ID GPL6244
Series (2)
GSE85748 MRPL53, a New Candidate Gene for Orofacial Clefting, Identified Using an eQTL Approach [expression array]
GSE85817 MRPL53, a New Candidate Gene for Orofacial Clefting, Identified Using an eQTL Approach

Data table header descriptions
ID_REF
VALUE The hybridization intensity values were background corrected, log2 transformed and then quantile normalized. We removed batch effects from log2 RMA data using an empirical Bayesian method (ComBat, parametric test; Johnson WE et al. 2007).

Data table
ID_REF VALUE
7896759 5.716911556
7896761 5.704988636
7896779 5.92129841
7896798 6.045288016
7896817 5.985581671
7896822 6.975307929
7896859 4.831450478
7896861 2.404150186
7896863 5.033519765
7896865 5.758127946
7896878 6.499023382
7896882 5.071495693
7896908 6.366217707
7896952 6.682845884
7896983 4.462700432
7896985 6.193579814
7897026 3.926835372
7897034 5.725615686
7897044 4.618332835
7897066 5.27151329

Total number of rows: 25506

Table truncated, full table size 495 Kbytes.




Supplementary file Size Download File type/resource
GSM2283461_F3434.CEL.gz 3.8 Mb (ftp)(http) CEL
Processed data included within Sample table
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap