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Sample GSM3983102 Query DataSets for GSM3983102
Status Public on Jul 26, 2022
Title JIA SFMCs child1
Sample type RNA
 
Source name Human mononuclear cells from patients with JIA isolated from synovial fluid
Organism Homo sapiens
Characteristics cell type: mononuclear cells from synovial fluid
disease state: Juvenile idiopathic arthritis
age: 9 years old
developmental stage: children
Treatment protocol not applicable
Growth protocol Human mononuclear cells from patients with JIA were isolated onto a Ficoll (PAN Biotech, Germany) gradient either from peripheral blood (PB) or synovial fluid (SF). Erythrocytes were lysed and cells were washed twice. Peripheral blood mononuclear cells (PBMC) were isolated from healthy donors by the same procedure. SF was obtained by incubation with hyaluronidase for 30 min. Following centrifugation at 400 x g for 10 min.
Extracted molecule total RNA
Extraction protocol miRNA extraction kit preAnalytix plus DNase digstion
Label biotin
Label protocol 1.5 µg of total RNA containing low molecular weight RNA was labelled using the FlashTag™ Biotin HSR RNA Labeling Kit according to the manufacturer’s instructions (ThermoFisher Scientific).
 
Hybridization protocol Each sample was hybridized to a GeneChip® miRNA 3.0 Array for 18 h at 48°C and 60 rpm (Affymetrix, Santa Clara, CA, USA). Afterwards, the chips were washed and stained on Fluidics Station 450 (Fluidics script FS450-0002).
Scan protocol Arrays were scanned on a GeneChip® Scanner 3000 7G (both, Affymetrix, Santa Clara, CA, USA).
Description miRNA
Data processing Data were analyzed by using expression console software 1.4 (Affymetrix, Santa Clara, CA, USA). The expression values were normalized with robust multi-array average (RMA).miRNA calculations and statistical significances between two groups (paired Student’s t-test) were performed with Transcriptome Analysis Console (TAC) Software (ThermoFisher Scientific). Detected miRNAs whose expression levels were significantly different (FDR-p value < 0.01) and showed a linear-fold change of at least 3.0, were considered as differentially expressed.
 
Submission date Jul 27, 2019
Last update date Jul 26, 2022
Contact name Bernd Denecke
E-mail(s) bernd.denecke@rwth-aachen.de
Phone +49 241 8089918
Organization name RWTH Aachen University
Department IZKF Aachen
Street address Pauwelsstrasse 30
City Aachen
State/province NRW
ZIP/Postal code 52074
Country Germany
 
Platform ID GPL16384
Series (1)
GSE134984 miR-23a regulates T cellular Redox metabolism in juvenile idiopathic arthritis

Data table header descriptions
ID_REF
VALUE log2 rma-dabg-Signal

Data table
ID_REF VALUE
hsa-miR-4732-3p_st 1.055477
hsa-miR-3200-5p_st 1.531985
hsa-miR-3158-3p_st 0.834491
hsa-miR-183_st 0.978953
hsa-miR-3200-3p_st 0.956149
hsa-miR-126_st 1.001277
hsa-miR-4685-3p_st 1.818022
hsa-miR-636_st 1.320216
hsa-miR-1255b_st 1.133734
hsa-miR-3158-5p_st 1.492831
hsa-miR-183-star_st 1.016208
hsa-miR-103a-2-star_st 1.063995
hsa-miR-331-5p_st 1.657056
hsa-miR-584_st 1.205447
hsa-miR-485-3p_st 1.576040
hsa-miR-3944-5p_st 0.796153
spike_in-control-31_st 15.840600
hsa-miR-130a_st 0.594895
hsa-miR-1254_st 2.223384
hsa-miR-1976_st 1.148887

Total number of rows: 5639

Table truncated, full table size 149 Kbytes.




Supplementary file Size Download File type/resource
GSM3983102_HOR_01_punctate_miRNA-3_0_.CEL.gz 801.4 Kb (ftp)(http) CEL
Processed data included within Sample table

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