|
Status |
Public on Aug 31, 2010 |
Title |
C2C12 growth condition, rep2 |
Sample type |
RNA |
|
|
Source name |
C2C12 growth
|
Organism |
Mus musculus |
Characteristics |
media: growth cell line: C2C12
|
Treatment protocol |
To induce differentiation, cells were switched to DMEM 2% horse serum (Sigma) after 10 h ( 100% confluency).
|
Growth protocol |
C2C12 cells were maintained at 20–70% confluency in Dulbecco’s Modified Eagles Medium (DMEM). supplemented with 10% fetal bovine serum.
|
Extracted molecule |
total RNA |
Extraction protocol |
Standard Affymetrix protocol
|
Label |
biotin
|
Label protocol |
Standard Affymetrix protocol
|
|
|
Hybridization protocol |
Standard Affymetrix protocol
|
Scan protocol |
Standard Affymetrix protocol
|
Description |
Cells collected at 60–70% confluency
|
Data processing |
We used the GC-bin method for background correction and applied quantile normalization. Probe set intensities and gene expression levels were derived from the probe logarithmic intensity error model (PLIER). MoEx-1_0-st-v1.r2.pgf MoEx-1_0-st-v1.r2.dt1.mm9.core.mps
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|
|
Submission date |
Aug 30, 2010 |
Last update date |
Aug 30, 2010 |
Contact name |
Zhe Ji |
E-mail(s) |
zhe.ji@northwestern.edu
|
Organization name |
Northwestern University
|
Street address |
303 E Superior St, Lurie 6-107
|
City |
Chicago |
State/province |
ILLINOIS |
ZIP/Postal code |
60611 |
Country |
USA |
|
|
Platform ID |
GPL6096 |
Series (1) |
GSE23871 |
Progressive lengthening of 3' untranslated regions of mRNAs by alternative polyadenylation during C2C12 differentiation |
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