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Sample GSM310594 Query DataSets for GSM310594
Status Public on Jun 01, 2009
Title Peripheral blood cells in patients with Systemic Lupus Erythematosus (SLE)-10
Sample type RNA
 
Channel 1
Source name Peripheral blood cells from SLE patient 10
Organism Homo sapiens
Characteristics Gender : female, Age : 54, 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.
 
Channel 2
Source name Peripheral blood cells from 12 healthy women
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.
 
 
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).
Description Genes expressed in peripheral blood cells from patients with SLE.
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.
 
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

Data table header descriptions
ID_REF
Validation Flag
VALUE Normalized log ratio (sample/reference)

Data table
ID_REF Validation VALUE
AGhsA010101 O 0.32
AGhsA010102 O 0.07
AGhsA010103 O -0.29
AGhsA010104 O 2.12
AGhsA010105 O 0.09
AGhsA010106 O -0.15
AGhsA010107 O -0.56
AGhsA010108 O -1.00
AGhsA010109 O -0.05
AGhsA010110 O -0.25
AGhsA010111 O -0.58
AGhsA010112 O -0.36
AGhsA010113 O -0.61
AGhsA010114 O 0.41
AGhsA010115 O -1.75
AGhsA010116 O 0.28
AGhsA010117 O 0.24
AGhsA010118 O -0.44
AGhsA010119 O -0.56
AGhsA010120 O -1.05

Total number of rows: 30336

Table truncated, full table size 575 Kbytes.




Supplementary file Size Download File type/resource
GSM310594.txt.gz 5.4 Mb (ftp)(http) TXT
Processed data included within Sample table

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