|
Status |
Public on Dec 31, 2012 |
Title |
Pleural and ascites fluids with chylothorax and an ITGA9 G404S mutation before OK-432 Ind-B |
Sample type |
RNA |
|
|
Channel 1 |
Source name |
Pleural fluid
|
Organism |
Homo sapiens |
Characteristics |
mutation: ITGA9 G404S treatment: No OK-432 treatment
|
Extracted molecule |
total RNA |
Extraction protocol |
Cell lines were lyzed by Trizol® Reagent (Invitrogen, USA) first, and purified by RNeasy Mini Kit (Qiagen, Germany). RNA isolated was quantified at OD260nm by using a ND-1000 spectrophotometer (Nanodrop Technology, USA) and qualitated by using a Bioanalyzer 2100 (Agilent Technology, USA) with RNA 6000 nano labchip kit (Agilent Technologies, USA).
|
Label |
Cy5
|
Label protocol |
0.2 mg of total RNA was amplified by a Low Input Quick-Amp Labeling kit (Agilent Technologies, USA) and labeled with Cy3 or Cy5 (CyDye, PerkinElmer, USA) during the in vitro transcription process.
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|
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Channel 2 |
Source name |
Ascites fluid
|
Organism |
Homo sapiens |
Characteristics |
mutation: ITGA9 G404S treatment: No OK-432 treatment
|
Extracted molecule |
total RNA |
Extraction protocol |
Cell lines were lyzed by Trizol® Reagent (Invitrogen, USA) first, and purified by RNeasy Mini Kit (Qiagen, Germany). RNA isolated was quantified at OD260nm by using a ND-1000 spectrophotometer (Nanodrop Technology, USA) and qualitated by using a Bioanalyzer 2100 (Agilent Technology, USA) with RNA 6000 nano labchip kit (Agilent Technologies, USA).
|
Label |
Cy3
|
Label protocol |
0.2 mg of total RNA was amplified by a Low Input Quick-Amp Labeling kit (Agilent Technologies, USA) and labeled with Cy3 or Cy5 (CyDye, PerkinElmer, USA) during the in vitro transcription process.
|
|
|
|
Hybridization protocol |
0.3 mg of Cy-labled cRNA was fragmented to an average size of about 50-100 nucleotides by incubation with fragmentation buffer at 60oC for 30 minutes. Correspondingly fragmented labeled cRNA is then pooled and hybridized to a SurePrint G3 Human GE 8×60K oligo microarray (Agilent Technologies, USA) at 65°C for 17 h.
|
Scan protocol |
Scanned on an Agilent G2565CA scanner, and images were quantified using Agilent Feature Extraction Software (version 10.5.1.1).
|
Description |
Transcriptional profile comparison of the pleural and ascites fluids in a fetal with chylothorax and an ITGA9 G404S mutation before OK-432 treatment
|
Data processing |
Agilent Feature Extraction Software (v 10.5.1.1) was used for background subtraction and LOWESS normalization.
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Submission date |
Feb 09, 2012 |
Last update date |
Dec 31, 2012 |
Contact name |
Gwo-Chin Ma |
E-mail(s) |
128729@cch.org.tw
|
Phone |
886-4-7238595
|
Fax |
886-4-7249847
|
Organization name |
Changhua Christian Hospital
|
Department |
Department of Genomic Medicine
|
Street address |
3F, 176, Zhanghua Rd.
|
City |
Changhua |
ZIP/Postal code |
500 |
Country |
Taiwan |
|
|
Platform ID |
GPL13607 |
Series (1) |
GSE33872 |
Human fetal chylothorax: pleural fluid vs. ascites fluid |
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