|
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. |
|