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Status |
Public on Sep 15, 2015 |
Title |
dicerwt_R1 Replicate 2 |
Sample type |
RNA |
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Source name |
RKO dicer wild-type cells
|
Organism |
Homo sapiens |
Characteristics |
genotype/variation: dicer wt transgene: cells expressing wild-type RNase1
|
Growth protocol |
Cells were cultured in serum-free PC-1 media (Lonza).
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA extracted using Trizol followed by two additional round of phenol-chloroform extraction.
|
Label |
Cy3,Cy5
|
Label protocol |
750 ng total RNA from both sample and reference was labeled with Hy3 and Hy5 fluorescent label, respectively, using the miRCURY LNA miRNA Hi-Power Labeling kit, Hy3/Hy5 (Exiqon,Denmark) following the procedure described by the manufaturer.
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Hybridization protocol |
The hybridization was performed according to the miRCURY LNA miRNA Array Instruction manual using a Tecan HS4800 hybridization station.
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Scan protocol |
The miRCURY LNA micro RNA Array slides were scanned using the Agilent G2565 BA Microarray Scanner System.
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Data processing |
The quantified signals were background corrected (Normexp with offset value 10) and normalized using the global Lowess regression algorithm. The normalized expression levels are expressed in a log2 scale.
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Submission date |
Sep 08, 2015 |
Last update date |
Sep 15, 2015 |
Contact name |
Emanuele Canestrari |
E-mail(s) |
manucns@uic.edu
|
Organization name |
University of Illinois at Chicago
|
Street address |
900 S. Ashland Ave.(M/C 669)
|
City |
Chicago |
ZIP/Postal code |
60607 |
Country |
USA |
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Platform ID |
GPL20891 |
Series (1) |
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