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Sample GSM5710870 Query DataSets for GSM5710870
Status Public on Feb 13, 2024
Title Donor 1; Sivelestat_High; 30 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 ID19933
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 8.354163183
P7 12.94720307
P9 13.11603507
P11 12.3330307
P13 13.19760734
P15 13.11620277
P17 12.60616461
P19 12.73149943
P21 13.42186698
P23 12.84754577
P25 12.94193217
P27 13.54414983
P29 8.946562895
P31 13.63051744
P33 13.67708203
P35 11.42832331
P37 14.14485285
P39 7.996928697
P41 9.645271838
P43 9.178049814

Total number of rows: 1350

Table truncated, full table size 23 Kbytes.




Supplementary file Size Download File type/resource
GSM5710870_HIPP_15_19933_.xlsx 1.8 Mb (ftp)(http) XLSX
Processed data included within Sample table

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