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Sample GSM2936311 Query DataSets for GSM2936311
Status Public on Aug 10, 2018
Title Neuromesodermal progenitors rep3
Sample type RNA
 
Source name hPSCs differentiated into the different anterior posterior populations at different time points as stated.
Organism Homo sapiens
Characteristics patient group: Neuromesodermal progenitors
Treatment protocol H9:SOX10 hPSCs were differentiated into neural crest cells and samples taken along timepoints of differentiation corresponding to neural plate border progenitor cell state or migratory neural crest cells. We utilised protocols to generate cells along the anterior posterior axis. First using all-trans retinoic acid, to mimic previous protocols to posteriorise cranial neural crest cells (CD6 for cranial and VD6 for RA patterned cells). We also compared these to neural crest cells derived from Neuromesodermal progenitors, that are present in the primitive streak and give rise to the posterior neural and mesodermal tissues. We compared these populations (TD6- trunk neural plate border cells; TD9- trunk migratory neural crest cells) to determine which showed more posterior gene expression patterns and assess determine any novel markers of hPSC derived neural crest cell populations.
Extracted molecule total RNA
Extraction protocol Direct-zol™ RNA MiniPrep (Zymo Research) was used for RNA extraction according to manufacturers' instructions
Label biotin
Label protocol Biotinylation of sense DNA fragments carried out according to Affymetrix protocol
 
Hybridization protocol 5.2µg of fragmented and biotinylated DNA molecules were applied to the Human Clariom D GeneChip in a hybridisation solution according to the Affymetrix protocol. Hybridisation took place overnight in a rotating hybridisation platform at 45°C for 16 hours. Post hybridisation stringency washing was done using the Affymetrix fluidics station again following the protocol outlined in the Affymetrix instructions
Scan protocol Scanned on an Affymetrix® GeneChip Scanner 3000 according to manufacturer's protocols
Description Differentiated H9:SOX10 hPSCs
Data processing Data were analysed using the Affymetrix TAC software
 
Submission date Jan 16, 2018
Last update date Aug 11, 2018
Contact name Paul Roy Heath
E-mail(s) [email protected]
Phone +44 114 2222254
Organization name University of Sheffield
Department Academic Neurology Unit
Lab Heath
Street address SITraN, 385a Glossop Road
City Sheffield
State/province S. Yorks
ZIP/Postal code S10 2HQ
Country United Kingdom
 
Platform ID GPL23126
Series (1)
GSE109267 Axial progenitors generate trunk neural crest cells in vitro

Data table header descriptions
ID_REF
VALUE RMA

Data table
ID_REF VALUE
TC0100006432.hg.1 3.613051
TC0100006433.hg.1 3.874782
TC0100006434.hg.1 5.653049
TC0100006435.hg.1 2.770346
TC0100006436.hg.1 3.357447
TC0100006437.hg.1 3.710424
TC0100006438.hg.1 6.713924
TC0100006439.hg.1 5.011449
TC0100006440.hg.1 2.995365
TC0100006441.hg.1 5.570749
TC0100006442.hg.1 4.516903
TC0100006443.hg.1 4.302613
TC0100006444.hg.1 4.16526
TC0100006445.hg.1 4.802127
TC0100006446.hg.1 3.754368
TC0100006447.hg.1 16.59362
TC0100006448.hg.1 5.223208
TC0100006449.hg.1 3.312241
TC0100006450.hg.1 3.864911
TC0100006451.hg.1 4.972629

Total number of rows: 138745

Table truncated, full table size 3668 Kbytes.




Supplementary file Size Download File type/resource
GSM2936311_19_TA_3.5_Clariom_D_Human_.CEL.gz 24.6 Mb (ftp)(http) CEL
Processed data included within Sample table

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