|
Status |
Public on Jun 09, 2023 |
Title |
X8a |
Sample type |
SRA |
|
|
Source name |
K562 cell line
|
Organism |
Homo sapiens |
Characteristics |
cell line: K562 cell line cell type: lymphoblast cells genotype: Cas9FCPF-sgRNA treatment: JQ1-FCPF time: 1h
|
Treatment protocol |
Transfected with Cas9FCPF with/without sgRNA 1 µM JQ1 or 1 µM JQ1-FCPF
|
Growth protocol |
K562 cells were maintained in DMEM supplemented with 10% fetal bovine serum (FBS) and antibiotics in humidified atmosphere with 5% CO2 at 37C
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was extracted with Trizol reagent, Quality control and sequencing were performed by Azenta
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2500 |
|
|
Data processing |
RNA seq was performed by Azenta
|
|
|
Submission date |
May 10, 2023 |
Last update date |
Jun 09, 2023 |
Contact name |
Xinlai Cheng |
E-mail(s) |
Cheng@pharmchem.uni-frankfurt.de
|
Organization name |
Goethe university Frankfurt
|
Department |
Pharmaceutical Chemistry
|
Street address |
Max-von-Laue-Strasse 15. R. 3.652
|
City |
Frankfurt |
ZIP/Postal code |
D-60438 |
Country |
Germany |
|
|
Platform ID |
GPL16791 |
Series (1) |
GSE232132 |
Chem-CRISPR/dCas9 -a chemically induced platform for epigenome editing |
|
Relations |
BioSample |
SAMN35019518 |
SRA |
SRX20275797 |