NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM4094918 Query DataSets for GSM4094918
Status Public on Sep 14, 2020
Title erythroid cell obtained from CD34 culture - 48h - DMSO DMSO_t1.CEL
Sample type RNA
 
Source name erythroid cell obtained from CD34 culture
Organism Homo sapiens
Characteristics time: 48h
Treatment protocol CX-5461 or vehicle were used on erythroid cell obtained from CD34 culture
Growth protocol Human CD34+ progenitors were purified from cord blood units on MidiMacs system (Miltenyi Biotech, Bergisch Gladbach, Germany). Murine Extensively Self-Renewing Erythroblasts (ESREs) were derived from fetal livers. Cell differentiation was followed by cytological examination and by flow cytometry (see supplemental material).
Extracted molecule total RNA
Extraction protocol RNA was extracted using the Kit QIAamp® RNA Blood MiniKit. RNA from ribosomal fractions was purified using Trizol (Invitrogen).
Label biotin
Label protocol Briefly, linear amplification of 20 ng of total RNA was performed using the Ovation Biotin RNA Amplification and Labelling System (NuGEN, San Carlos, CA).
 
Hybridization protocol cDNA was hybridized to HTA2.0 affymetrix microarrays following standard
Scan protocol affymetrix microarrays following standard
Description erythroid cell obtained from CD34 culture - 48h - DMSO
erythroid cell obtained from CD34 culture
Data processing Raw expression values were normalized using Robust Multiarray Averaging (RMA)
 
Submission date Sep 24, 2019
Last update date Sep 15, 2020
Contact name Ismael Boussaid
E-mail(s) [email protected]
Phone +33618115659
Organization name Inserm
Lab Institut Cochin
Street address 22 Rue Mechain
City Paris
ZIP/Postal code 75014
Country France
 
Platform ID GPL22936
Series (2)
GSE137951 p53 activation during ribosome biogenesis regulates normal erythroid differentiation. [expression]
GSE157210 p53 activation during ribosome biogenesis regulates normal erythroid differentiation.

Data table header descriptions
ID_REF
VALUE RMA signal intensity

Data table
ID_REF VALUE
1_at 6.41555021303185
10_at 3.9857566063257
100_at 7.23973583148994
1000_at 4.08978295711913
10000_at 4.94148522706415
100009601_at 8.91056368481432
100009613_at 4.66957971140511
100009676_at 5.95620549303711
10001_at 8.54595821088492
10002_at 5.39196547741926
10003_at 3.20063811111674
100033411_at 3.21544014121844
100033413_at 4.4931634184615
100033414_at 4.10247651069449
100033416_at 6.00229492934171
100033418_at 3.47279063124285
100033420_at 4.64288081224863
100033422_at 3.15561725936314
100033423_at 4.20089095722627
100033424_at 3.31504698842226

Total number of rows: 25736

Table truncated, full table size 665 Kbytes.




Supplementary file Size Download File type/resource
GSM4094918_DMSO_t1.CEL.gz 26.5 Mb (ftp)(http) CEL
Processed data included within Sample table

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