|
| Status |
Public on May 31, 2012 |
| Title |
Day 25 Male replicate 6 [e13] |
| Sample type |
RNA |
| |
|
| Channel 1 |
| Source name |
universal SoNG reference
|
| Organism |
Taeniopygia guttata |
| Characteristics |
brain region: Telencephalon
age: Adult
gender: Male and Female
treatment protocol: Whole telencephalon pool of 30 birds (15 males and 15 females) supplied equally from each of 5 aviaries around the country
|
| Treatment protocol |
LMAN punches were taken from frozen brain sections of Taeniopygia guttata males at post-hatch days 25 and 45.
|
| Extracted molecule |
total RNA |
| Extraction protocol |
Experimental samples: Total RNA was extracted using Absolutely RNA Microprep kit (Stratagene). 500ng total RNA wasamplified using Agilent's Low RNA input linear amplification kit. Universal reference: Total RNA was extracted using Trizol following manufacturer's protocol; samples were Dnase treated and cleaned on a spin column; equal amounts of total RNA from each bird was pooled; total RNA was amplified from this pool using Agilent's Low RNA input linear amplification kit to create sufficient aRNA for 5000 assays.
|
| Label |
Cy5
|
| Label protocol |
1 µg of aRNA was primed with 3 µl of 100 µM random hexamer primers at 70°C for 10 min, then reversed transcribed at 46°C for 16 h in the presence of 400 U SuperScript II RTase (Invitrogen), and 100 µM dATP, dCTP, dGTP, 60µM dTTP and 40µM aa-dUTP; RNA was hydrolyzed in the presence of NaOH and EDTA and samples were cleaned up on a spin column. Finally, Cy3 and Cy5 dye esters (GE Healthcare) were coupled to aa-dUTP residues in NaCO3 buffer for 2 hrs at room temp, then neutralized and cleaned on spin columns.
|
| |
|
| Channel 2 |
| Source name |
Day 25 Male
|
| Organism |
Taeniopygia guttata |
| Characteristics |
brain region: LMAN
age: Post-hatch day 25
gender: Male
treatment protocol: LMAN punch dissection
|
| Treatment protocol |
LMAN punches were taken from frozen brain sections of Taeniopygia guttata males at post-hatch days 25 and 45.
|
| Extracted molecule |
total RNA |
| Extraction protocol |
Experimental samples: Total RNA was extracted using Absolutely RNA Microprep kit (Stratagene). 500ng total RNA wasamplified using Agilent's Low RNA input linear amplification kit. Universal reference: Total RNA was extracted using Trizol following manufacturer's protocol; samples were Dnase treated and cleaned on a spin column; equal amounts of total RNA from each bird was pooled; total RNA was amplified from this pool using Agilent's Low RNA input linear amplification kit to create sufficient aRNA for 5000 assays.
|
| Label |
Cy3
|
| Label protocol |
1 µg of aRNA was primed with 3 µl of 100 µM random hexamer primers at 70°C for 10 min, then reversed transcribed at 46°C for 16 h in the presence of 400 U SuperScript II RTase (Invitrogen), and 100 µM dATP, dCTP, dGTP, 60µM dTTP and 40µM aa-dUTP; RNA was hydrolyzed in the presence of NaOH and EDTA and samples were cleaned up on a spin column. Finally, Cy3 and Cy5 dye esters (GE Healthcare) were coupled to aa-dUTP residues in NaCO3 buffer for 2 hrs at room temp, then neutralized and cleaned on spin columns.
|
| |
|
| |
| Hybridization protocol |
Samples were suspended in SlideHyb#1 (Ambion), applied to slides in Corning Hybridization Chamber, and incubated O/N at 42˚C. After hybridization, the slides were washed sequentially in 1X SSC, 0.2% SDS; 0.1X SSC, 0.2% SDS; and 0.1X SSC for 5 minutes each, and spun dry.
|
| Scan protocol |
Scanned on an Axon GenePix 4000B scanner
Images were quantified using Axon Genepix 6.0
|
| Description |
Biological replicate 6 of 8 Male Post-hatch day 25
|
| Data processing |
Data were background-subtracted and values < 0.5 were set to 0.5. Spots with -100 flags were filtered out before print-tip loess normalization. A scale between-array normalization was performed, then arrays with the reference in the Cy5 channel were inverted by multiplying by -1 to make all log ratios test/reference.
|
| |
|
| Submission date |
Mar 23, 2012 |
| Last update date |
May 31, 2012 |
| Contact name |
Kirstin Replogle |
| E-mail(s) |
replogle@igb.uiuc.edu
|
| Organization name |
University of Illinois
|
| Street address |
1206 W Gregory Drive
|
| City |
Urbana |
| State/province |
IL |
| ZIP/Postal code |
61801 |
| Country |
USA |
| |
|
| Platform ID |
GPL9554 |
| Series (2) |
| GSE36744 |
The impact of experience-dependent and independent factors on gene expression in songbird brain [e13] |
| GSE36748 |
The impact of experience-dependent and independent factors on gene expression in songbird brain |
|
