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Status |
Public on Jun 18, 2018 |
Title |
THP1 SAMHD1 KO 3 |
Sample type |
RNA |
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|
Source name |
Generated by using a CRISPR-Cas9 lentiviral vector expressing gRNA specific for SAMHD1
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Organism |
Homo sapiens |
Characteristics |
cell line: THP1 cell type: Patient-derived acute myeloid leukemia cells genotype/variation: SAMHD1 KO
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Growth protocol |
Cells were grown in RPMI 1640 (ATCC) supplemented with 10% FBS, 100 U/ml penicillin, 100 μg/ml streptomycin and 1 μg/ml puromycin. 500,000 cells/well were seeded in 12-well plate in 1 ml/well, and harvested after 48 hours. Three replicates were prepared for each cell line.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted using the RNeasy Mini kit (Qiagen)
|
Label |
biotin
|
Label protocol |
Experiment performed at: Genomic Core Facility, The Ohio State University, Columbus, Ohio, USA.
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Hybridization protocol |
Experiment performed at: Genomic Core Facility, The Ohio State University, Columbus, Ohio, USA.
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Scan protocol |
Experiment performed at: Genomic Core Facility, The Ohio State University, Columbus, Ohio, USA.
|
Description |
Replicate #3
|
Data processing |
The data were normalized by RMA method with Affymetrix Expression Console software. Normalized data were filtered by keeping genes whose expression are above 6 (log2 scale) for at least 2 out of 3 samples in any condition. Linear model and moderated t-test was used for testing differentially expressed genes by using SAS and R packages.
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Submission date |
Apr 24, 2018 |
Last update date |
Jun 19, 2018 |
Contact name |
Serena Bonifati |
E-mail(s) |
[email protected]
|
Organization name |
Ohio State University College of Veterinary Medicine
|
Department |
Veterinary Biosciences
|
Lab |
Dr. Li Wu
|
Street address |
1900 Coffey Road
|
City |
Columbus |
State/province |
Ohio |
ZIP/Postal code |
43210 |
Country |
USA |
|
|
Platform ID |
GPL23126 |
Series (1) |
GSE113610 |
Microarray analysis in acute myeloid leukemia (AML)-derived THP-1 cells expressing or not SAMHD1 |
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