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Sample GSM5710864 Query DataSets for GSM5710864
Status Public on Feb 13, 2024
Title Donor 1; Telaprevir_Low; 10 min
Sample type protein
 
Source name Human islets
Organism Homo sapiens
Characteristics diabetes status: Non-diabetic
unos id/rrid: SAMN09768368
date of treatment: 8.8.18
Treatment protocol Human islets were starved in Final Wash media for 3 hours. After, IEQs were treated with DMSO, telaprevir (1 and 100 µg/ml), tebipenem (1 and 100 µg/ml), sivelestat (100 µg/ml), 5-IT (1 µM), Ovalbumin (1 µg/ml) and SerpinB1 (1 µg/ml) for 10 or 30 minutes. At the end of the incubation, islets were collected and washed once in PBS. Finally islet pellet was snap-frozen in liquid nitrogen.
Growth protocol Human islets were obtained by Prodo Lab or IIDP. Upon receipt, human islets were cultured in Miami Media at 37 C 5% CO2. After overnight incubation, 150/200 size-matched IEQs per condition were hand-picked for the following procedure
Extracted molecule protein
Extraction protocol Total proteins were harvested from islets lysates using M-PER protein extraction reagent (Thermo Fisher, USA) supplemented with proteinase and phosphatase inhibitors (Sigma, USA) according to standard protocol.
Label biotin
Label protocol Proteins were covalently labeled with biotin. Free biotin molecules are then removed at the completion of labeling reactions by gel filtration.
 
Hybridization protocol After blocking non-specific binding sites on the array, an incubation chamber is mounted onto the microarray to permit the loading of 2 samples side by side on the same chip and prevent mixing of the samples. Following sample incubation, unbound proteins are washed away and the array is then probed with anti-biotin antibody that is labelled with a proprietary fluorescent dye combination.
Scan protocol Each array produces a pair of 16-bit images, which are captured with a Perkin-Elmer ScanArray Reader laser array scanner (Waltham, MA).
Description ID19920
Data processing Signal quantification is performed with ImaGene 9.0 from BioDiscovery (El Segundo, CA) with predetermined settings for spot segmentation and background correction. The background-corrected raw intensity data are logarithmically transformed with base 2.
 
Submission date Dec 02, 2021
Last update date Feb 13, 2024
Contact name Jonathan M Dreyfuss
Organization name Joslin Diabetes Center
Department Bioinformatics & Biostatistics Core
Street address 1 Joslin Pl
City Boston
State/province MA
ZIP/Postal code 02215
Country USA
 
Platform ID GPL26730
Series (1)
GSE189986 Short-term effects of Elastase inhibition on human islets protein phosphorylation

Data table header descriptions
ID_REF
VALUE Normalized and logarithmically transformed signal intensity.

Data table
ID_REF VALUE
P5 7.44324335
P7 13.06994052
P9 13.0922407
P11 12.5627065
P13 13.23430762
P15 13.10964615
P17 12.53872794
P19 12.42711283
P21 13.41568967
P23 12.90191254
P25 13.18345953
P27 13.66770709
P29 8.666660146
P31 13.92850315
P33 13.60566229
P35 11.06034184
P37 14.11118856
P39 7.572249305
P41 9.256019418
P43 8.345757959

Total number of rows: 1350

Table truncated, full table size 23 Kbytes.




Supplementary file Size Download File type/resource
GSM5710864_HIPP_2_19920_.xlsx 1.8 Mb (ftp)(http) XLSX
Processed data included within Sample table

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