|
Status |
Public on Feb 20, 2023 |
Title |
R2 |
Sample type |
SRA |
|
|
Source name |
bone marrow-derived monocytes (BMDMs)
|
Organism |
Mus musculus |
Characteristics |
strain: C57BL/6 cell type: bone marrow-derived monocytes (BMDMs) treatment: M-CSF, RANKL
|
Treatment protocol |
For osteoclast induction, BMDMs were cultured into complete media with 50 ng/ml recombinant soluble murine M-CSF (PeproTech, 315-02),100 ng/ml recombinant soluble murine RANKL. Then the cells were treated with either vehicle or dBRD9, JQ1, DEX, iBRD9.
|
Growth protocol |
Bone marrow cells were harvested from murine tibias and femurs of C57BL/6 mice and cultured in α-minimum essential medium containing 10% FBS and 1% penicillin-streptomycin overnight.
|
Extracted molecule |
total RNA |
Extraction protocol |
BMDMs was collected for RNA isolation using TRIzol. Libraries were prepared using NEBNext Ultra II RNA Library Prep Kit
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NovaSeq 6000 |
|
|
Data processing |
Raw reads were trimmed using Cutadapt. Trimmed reads were aligned with the GRCm39 genome using HISAT2 Read count extraction and normalization were performed using htseq-count. Assembly: Mus_musculus.GRCm39. Supplementary files format and content: Excel files include read count and fpkm values for each sample
|
|
|
Submission date |
Jan 05, 2023 |
Last update date |
Feb 20, 2023 |
Contact name |
Jiahui Du |
E-mail(s) |
[email protected]
|
Organization name |
Shanghai Jiao Tong University
|
Street address |
Zhizaoju Road 639
|
City |
Shanghai |
ZIP/Postal code |
90033 |
Country |
China |
|
|
Platform ID |
GPL24247 |
Series (2) |
GSE222239 |
Function of BRD9 during osteoclastogenesis [RNA-seq-2] |
GSE222240 |
Function of BRD9 during osteoclastogenesis |
|
Relations |
BioSample |
SAMN32601390 |
SRA |
SRX18944607 |