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Sample GSM2355565 Query DataSets for GSM2355565
Status Public on Mar 14, 2017
Title Immature_T_cells_CD34+_day_0_Start
Sample type RNA
 
Source name Immature T-cells, CD34+, day 0, Start
Organism Homo sapiens
Characteristics tissue: cord blood
timecourse: 0 day
Biomaterial provider Hokkaido Cord Blood Bank
Treatment protocol Cells were harvested with TRIzol (Sigma, Aldrich).
Growth protocol CD34+ cells were isolated from CB using CD34 MicroBead Kit (Miltenyi Biotech)
Extracted molecule total RNA
Extraction protocol RNA was prepared using the RNAeasy column purification (QIAGEN, Valencia, CA) following the manufacturer's recommendations. RNA was quantified using a NanoDrop-1000 spectrophotometer and quality was monitored with the Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA).
Label Cy3-pCp
Label protocol Sample labeling was performed as detailed in the “miRNA Microarray System with miRNA Complete Labeling and Hyb Kit” protocol (version 2.4, part number G4170-90011). Briefly, 90 ng total RNA of sample hES d0 Pool and 100 ng total RNA of all other samples was used for the labeling step using the miRNA Complete Labeling and Hyb Kit (Agilent Technologies).
 
Hybridization protocol The hybridization procedure was performed according to the “miRNA Complete Labeling and Hyb Kit” protocol using the miRNA Complete Labeling and Hyb Kit (Agilent Technologies). Briefly, Cy3-labeled RNA in hybridization buffer was hybridized overnight (20 hours, 55 °C) to Agilent Human microRNA Microarrays 8x60K v19 (Design ID 046064) using Agilent’s recommended hybridization chamber and oven. Following hybridization, the microarrays were washed once with the Agilent Gene Expression Wash Buffer 1 for 5 min at room temperature followed by a second wash with preheated Agilent Gene Expression Wash Buffer 2 (37 °C) for 5 min.
Scan protocol Fluorescence signals of the hybridized Agilent Microarrays were detected using Agilent’s Microarray Scanner System (G2505C, Agilent Technologies, Palo Alto, USA).
Description Micro RNA expression from immature T-cells with CD34+ at day 0 after the beginning of differentiation
Data processing The Agilent Feature Extraction Software (FES 10.7.3.1 ) was used to read out and process the microarray image files.
 
Submission date Oct 19, 2016
Last update date Mar 14, 2017
Contact name Toutai MITUYAMA
Organization name National Institute of Advanced Industrial Science and Technology (AIST)
Department Artificial Intelligence Research Team
Lab Computational Omics Research Team
Street address 2-4-7 Aomi
City Koto-ku
State/province Tokyo
ZIP/Postal code 135-0064
Country Japan
 
Platform ID GPL19730
Series (2)
GSE88936 Time series micro RNA analysis of immature T-cells and reMAIT cells by microarrays
GSE88938 Time series transcriptome and DNA methylome analysis of immature T-cells and reMAIT cells

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
A_25_P00010019 21.27864636
A_25_P00010020 16.81454104
A_25_P00010021 17.72280746
A_25_P00010023 17.61452782
A_25_P00010041 13.18262661
A_25_P00010042 15.16409769
A_25_P00010043 14.03261258
A_25_P00010044 15.55460196
A_25_P00010047 17.31182736
A_25_P00010048 16.35891965
A_25_P00010053 18.24638318
A_25_P00010054 18.37776339
A_25_P00010062 16.04840627
A_25_P00010063 16.03436977
A_25_P00010070 71.07655341
A_25_P00010071 51.47655341
A_25_P00010072 67.90988674
A_25_P00010073 34.87655341
A_25_P00010078 22.70991166
A_25_P00010079 17.3800677

Total number of rows: 4774

Table truncated, full table size 125 Kbytes.




Supplementary file Size Download File type/resource
GSM2355565_CB_CD34.txt.gz 8.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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