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Status |
Public on Aug 26, 2013 |
Title |
Injected C.albicans in zebrafish_8hpi_rep1 |
Sample type |
RNA |
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Source name |
Injected C.albicans in zebrafish_8hpi
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Organism |
Candida albicans |
Characteristics |
post-infection time points: 8hpi
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Treatment protocol |
Each fish was intraperitoneally injected with 1×108 C. albicans cells suspended in 10μL sterile 1× phosphate-buffered saline (PBS)
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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 |
0.625μg of Cy3 cRNA for C. albicans 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 8hr in injected C. albicans in infected 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 |
Sep 14, 2011 |
Last update date |
Aug 26, 2013 |
Contact name |
Yan-Yu Chen |
Organization name |
NTHU
|
Department |
Chemical Engineering
|
Lab |
Thermal Lab
|
Street address |
No. 101, Section 2, Kuang-Fu Road
|
City |
Hsin-chu |
ZIP/Postal code |
300 |
Country |
Taiwan |
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|
Platform ID |
GPL14575 |
Series (2) |
GSE32117 |
Host and pathogen interaction: time course [C. albicans] |
GSE32119 |
Host and pathogen interaction: time course |
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