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Status |
Public on Sep 11, 2017 |
Title |
L428_scr_rep3 |
Sample type |
RNA |
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|
Source name |
L428, Negative_Control_siRNA
|
Organism |
Homo sapiens |
Characteristics |
cell line: L428 perturbagen: Negative_Control_siRNA
|
Treatment protocol |
L428 were nucleofected with L solution following Lonza optimzalized protocol with either 3ug BATF3siRNA or control siRNA and cultivated for 48 hours.
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Growth protocol |
RPMI1640, 10% FCS, 1% pen/strep
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA extraction was performed with Qiagen RNeasy Mini Kit
|
Label |
Biotin
|
Label protocol |
Biotinylated cRNA were prepared according to the standard Affymetrix protocol from total RNA
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|
|
Hybridization protocol |
Fragmented cRNA was hybridized to PrimeView array using Affymetrix standard protocol
|
Scan protocol |
Affymetrix Standard protocol Affymetrix Standard protocol
|
Description |
Gene expression data of L428 cells treated with negative control siRNA
|
Data processing |
Probe level quantile normalisation and robust multi-array analysis on the raw CEL files were performed using the affy package of the Bioconductor project.
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|
|
Submission date |
Nov 10, 2016 |
Last update date |
Sep 11, 2017 |
Contact name |
Wenbin Wei |
E-mail(s) |
[email protected]
|
Organization name |
Durham University
|
Department |
Biosciences
|
Street address |
Stockton Road
|
City |
Durham |
ZIP/Postal code |
DH1 3LE |
Country |
United Kingdom |
|
|
Platform ID |
GPL16043 |
Series (1) |
GSE89760 |
BATF3siRNA induced gene expression changes in Hodgkin lymphoma cell line L428. |
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