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Status |
Public on Jun 01, 2009 |
Title |
Peripheral blood cells in patients with Systemic Lupus Erythematosus (SLE)-5 |
Sample type |
RNA |
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Channel 1 |
Source name |
Peripheral blood cells from SLE patient 5
|
Organism |
Homo sapiens |
Characteristics |
Gender : female, Age : 32, Disease : Systemic Lupus Erythematosus
|
Extracted molecule |
total RNA |
Extraction protocol |
Peripheral blood was collected directly into PAXGene tubes (Qiagen, Valencia, CA). Total RNA was extracted using PAXGene Blood RNA kit with the optimal on-column DNase digestion according to the manufacturer's instructions.
|
Label |
Cy3
|
Label protocol |
Total RNA was amplified. 5-(3-amino allyl)-UTP was incorporated to it using Amino Allyl MessageAmp aRNA kit (Ambion, Austin, Texas). The amino allyl aRNA was further labeled by coupling reaction with NHS ester fluorescent dye, Cy3.
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Channel 2 |
Source name |
Peripheral blood cells from 12 healthy women
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Organism |
Homo sapiens |
Characteristics |
Healthy women without any identified diseases.
|
Extracted molecule |
total RNA |
Extraction protocol |
Peripheral blood was collected directly into PAXGene tubes (Qiagen, Valencia, CA). Total RNA was extracted using PAXGene Blood RNA kit with the optimal on-column DNase digestion according to the manufacturer's instructions.
|
Label |
Cy5
|
Label protocol |
Total RNA was amplified. 5-(3-amino allyl)-UTP was incorporated to it using Amino Allyl MessageAmp aRNA kit (Ambion, Austin, Texas). The amino allyl aRNA was further labeled by coupling reaction with NHS ester fluorescent dye, Cy5.
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Hybridization protocol |
The labeled aRNAs (mixture of Cy3 and Cy5) was hybridized onto microarray slide for 16 hours at 42℃. Slides were washed in 2xSSC+0.1% SDS, 2xSSC, 1xSSC and 0.1xSSC before air pressure drying and scanning.
|
Scan protocol |
Fluorescent array images were collected for both Cy3 and Cy5 with a ScanArray Lite (PerkinElmer, Boston, MA) and signal values were calculated using DNASIS Array (Hitachi Software Engineering, Tokyo, Japan).
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Description |
Genes expressed in peripheral blood cells from patients with SLE.
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Data processing |
The median background intensities were subtracted from median intensities of Channel 1 (Cy3) or Channel 2 (Cy5). Log2 ratios of Cy3 to Cy5 were calculated. The VALUE shown were log2 Cy3/Cy5 ratios of all spots on the DNA microarray which were normalized by the method of global ratio median normalization.
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Submission date |
Aug 07, 2008 |
Last update date |
Jun 01, 2009 |
Contact name |
Norihiro Nishimoto |
E-mail(s) |
norichan@wakayama-med.ac.jp
|
Phone |
+81-72-646-8039
|
Fax |
+81-72-646-8140
|
Organization name |
Wakayama Medical University
|
Lab |
Laboratory of Immune Regulation
|
Street address |
7-7-20, Saito-Asagi
|
City |
Ibaraki |
State/province |
Osaka |
ZIP/Postal code |
567-0085 |
Country |
Japan |
|
|
Platform ID |
GPL1291 |
Series (1) |
GSE12374 |
Interactions of cytokines in peripheral blood cells from Systemic Lupus Erythematosus |
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