Automated Author ProfileJung, Jinjoo
0000-0001-5809-5792
Jung, Jinjoo
Current S-Index
Sum of Dataset Indices for all datasets
Average Dataset Index per Dataset
Average Dataset Index per dataset
Total Datasets
Total datasets for this author
Average FAIR Score
Average FAIR Score per dataset
Total Citations
Total citations to the author's datasets
Total Mentions
Total mentions of the author's datasets
S-Index Interpretation
The S-Index (Sharing Index) is a comprehensive metric that represents the cumulative impact of all your datasets. It is calculated as the sum of Dataset Index scores across all your claimed datasets.
What it means:
- A higher S-index indicates greater overall impact of your datasets relative to typical datasets in their fields of research
- The S-Index grows as you add more datasets or as existing datasets gain more citations and mentions
- It provides a single number to track your research data impact over time
Current S-Index: 2.2 (sum of 2 datasets Dataset Index scores)
More information here.
S-Index Over Time
Cumulative Citations Over Time
Cumulative Mentions Over Time
Datasets
Target protein identification study of SB2301, a small molecule that reduces cellular lipid droplets, was performed using the thermal stability shift-based fluorescence difference in two-dimensional gel electrophoresis (TS-FITGE) The protein spots from the silver-stained gel were excised, destained, and digested with trypsin. The mixture was evaporated in SpeedVac and then dissolved in 10% acetonitrile with 0.1% formic acid. The resulting peptides were desalted in a trap column (180 μm × 20 mm, Symmetry C18) and separated on a C18 reversed-phase analytical column (75 μm × 200 mm, 1.7 μm, BEH130 C18) (Waters) with an electrospray ionization Pico Tip (±10 μm i.d.) [New objective]. The data were converted to .pkl files by Protein Lynx Global Server and searched by MASCOT engine with the SwissProt database.
Authors
- Jung, Jinjoo ;
- Park, Seung Bum
Target protein identification study of SB2301, a small molecule that reduces cellular lipid droplets, was performed using the thermal stability shift-based fluorescence difference in two-dimensional gel electrophoresis (TS-FITGE) The protein spots from the silver-stained gel were excised, destained, and digested with trypsin. The mixture was evaporated in SpeedVac and then dissolved in 10% acetonitrile with 0.1% formic acid. The resulting peptides were desalted in a trap column (180 μm × 20 mm, Symmetry C18) and separated on a C18 reversed-phase analytical column (75 μm × 200 mm, 1.7 μm, BEH130 C18) (Waters) with an electrospray ionization Pico Tip (±10 μm i.d.) [New objective]. The data were converted to .pkl files by Protein Lynx Global Server and searched by MASCOT engine with the SwissProt database.
Authors
- Jung, Jinjoo ;
- Park, Seung Bum