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Status |
Public on Apr 02, 2018 |
Title |
Ventricular resection zebrafish_15dpi |
Sample type |
RNA |
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Source name |
Ventricular resection-injured zebrafish, 15dpi
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Organism |
Danio rerio |
Characteristics |
tissue: Heart gender: male age: 1 year
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Treatment protocol |
Not applicable.
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Growth protocol |
Not applicable
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Extracted molecule |
total RNA |
Extraction protocol |
RNA was prepared using the RNeasy Mini Kit (Qiagen, Germany) following the manufacturer's recommendations. RNA purified was quantified at OD260nm by using a ND-1000 spectrophotometer (Nanodrop Technology, USA) and qualitated by Bioanalyzer 2100 (Agilent Technology, USA) with RNA 6000 nano labchip kit (Agilent Technologies, USA).
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Label |
Cy3
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Label protocol |
1.65 μg of Cy3 cRNA for zebrafish array was fragmented to an average size of about 50-100 nucleotides by incubation with fragmentation buffer at 60°C for 30 minutes.
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Hybridization protocol |
The fragmented labeled cRNA was then hybridized to oligo microarray at 60°C for 17 h.
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Scan protocol |
After washing and drying by nitrogen gun blowing, microarrays are scanned with an Agilent microarray scanner (Agilent Technologies, USA) at 535 nm for Cy3.
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Description |
Gene expression after 15dpi in ventricular resection-injured zebrafish
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Data processing |
Scanned images are analyzed by Feature extraction 9.5.3 software (Agilent Technologies, USA), image analysis and normalization software is used to quantify signal and background intensity for each feature.
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Submission date |
Aug 25, 2015 |
Last update date |
Apr 02, 2018 |
Contact name |
Yung-Jen Chuang |
E-mail(s) |
yjchuang@life.nthu.edu.tw
|
Phone |
886-3-574-2764
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Organization name |
National Tsing Hua University
|
Department |
Department of Medical Science
|
Lab |
YJ Chuang
|
Street address |
No. 101, Sec. 2, Kuang Fu Road
|
City |
Hsinchu |
State/province |
Taiwan |
ZIP/Postal code |
30013 |
Country |
Taiwan |
|
|
Platform ID |
GPL6457 |
Series (1) |
GSE72348 |
Wound healing process after ventricular resection in zebrafish: time course (zebrafish) |
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