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Sample GSM1099451 Query DataSets for GSM1099451
Status Public on Jun 01, 2013
Title HEMa_p_plus_3_ii
Sample type RNA
 
Source name Primary melanocytes, WT
Organism Homo sapiens
Characteristics cell type: primary melanocytes
cell stage: melanocytes
genotype: WT
day of collection/passage: passage 3
clone: n/a
Treatment protocol hESCs were plated on matrigel for differentiation and grown in the presence of 100 nM LDN-193189, 10 uM SB431542, 3 uM CHIR 99021 (Stemgent), 25 ng/ml BMP4 (R&D) and 100nM EDN3 (American Peptide Company) for BE. Cells were dissociated at day 11 and replated on poly-ornithine-, laminin-, and fibronectin-coated plates in NB/Mel media. NB/Mel media was prepared by replacing the WNT3A-CM component in Mel-1 media (Fang et al., 2006) with Neurobasal (Invitrogen) medium containing 2% B27 supplement (Invitrogen), 3μM Chir, 25 ng/ml BMP4, and 500 μM dbcAMP. Cells were fed every other day and passaged weekly for maintenance and expansion.
Growth protocol hESCs (WA09; passages 32-50) were cultured with mouse embryonic fibroblasts (MEFs, Globalstem) pre-plated at 12-15,000 cells/cm2. hESC cells were grown in DMEM:F12 hESC media containing 6ng/mL FGF2 and passaged using dispase or accutase. Primary melanocytes were maintained in M254 media with HMGS supplement (Invitrogen).
Extracted molecule total RNA
Extraction protocol RNA was extracted with Trizol reagent, followed by clean-up and DNase I treatment with the QIAGEN RNeasy mini kit in accordance with the prescribed protocol provided with the kit. Quality control was performed with an Agilent Bioanalyser.
Label biotin
Label protocol Biotinylated cRNA were prepared with the Ambion MessageAmp kit for Illumina arrays.
 
Hybridization protocol Standard Illumina hybridization protocol.
Scan protocol Standard Illumina scanning protocol.
Description Replicate 2.
Data processing The data were normalised using quantile normalisation in Partek Genomics Suite software.
 
Submission date Mar 15, 2013
Last update date Jun 01, 2013
Contact name Yvonne Mica
E-mail(s) grubery@mskcc.org
Organization name Memorial Sloan-Kettering Cancer Center
Street address 1275 York Avenue
City New York
State/province NY
ZIP/Postal code 10021
Country USA
 
Platform ID GPL10904
Series (2)
GSE45226 Genome-wide analysis of gene expression in human pluripotent stem cell-derived melanocyte progenitors, mature melanocytes, and disease-specific melanocytes
GSE45227 Genome-wide analysis of gene expression in melanocytes derived from human embryonic stem cells and patient specific induced pluripotent stem cells

Data table header descriptions
ID_REF
VALUE Quantile-normalized signal intensity

Data table
ID_REF VALUE
7A5 6.74051
A1BG 6.56282
A1CF 6.50683
A26C3 6.58074
A2BP1 6.42412
A2LD1 7.69352
A2M 8.81912
A2ML1 6.34618
A3GALT2 6.56316
A4GALT 6.34279
A4GNT 6.53651
AAA1 6.61113
AAAS 7.60138
AACS 7.33414
AACSL 6.86884
AADAC 6.40338
AADACL1 7.99871
AADACL2 6.5622
AADACL3 6.57555
AADACL4 6.63506

Total number of rows: 34694

Table truncated, full table size 543 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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