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Sample GSM3983107 Query DataSets for GSM3983107
Status Public on Jul 26, 2022
Title JIA SFMCs child6
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: 13-17 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 1.093458
hsa-miR-3200-5p_st 1.510161
hsa-miR-3158-3p_st 1.292256
hsa-miR-183_st 0.890959
hsa-miR-3200-3p_st 0.749282
hsa-miR-126_st 0.711818
hsa-miR-4685-3p_st 0.914781
hsa-miR-636_st 2.407560
hsa-miR-1255b_st 1.534657
hsa-miR-3158-5p_st 2.195250
hsa-miR-183-star_st 0.655592
hsa-miR-103a-2-star_st 0.734138
hsa-miR-331-5p_st 1.323210
hsa-miR-584_st 1.506036
hsa-miR-485-3p_st 1.517291
hsa-miR-3944-5p_st 1.124424
spike_in-control-31_st 15.833730
hsa-miR-130a_st 1.153558
hsa-miR-1254_st 2.406019
hsa-miR-1976_st 1.394276

Total number of rows: 5639

Table truncated, full table size 149 Kbytes.




Supplementary file Size Download File type/resource
GSM3983107_HOR_07_punctate_miRNA-3_0_.CEL.gz 777.8 Kb (ftp)(http) CEL
Processed data included within Sample table

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