The Award Winning New Measure of Productivity
ICON™ is the world’s first benchtop system measuring normalized titer for the characterization of high productivity clones in cell line development.
Winner of the SLAS New product Award, ICON uses on-board assays for the three critical quality attributes of titer, cell number and cell viability assessing productivity to enable rapid stratification of leading candidates.
Helping scientists focus on the winners, earlier, ICON slashes timelines and enhances success through meaningful data.
Viewing productivity by normalized titer
ICON combines titer with cell number enabling measures of specific productivity for both the static and expansion stages of cell line development.
ICON Plate-Based Titer
For cloning and expansion stages
- Rapid 96 well plate measurements
- Uses just 60 µl sample
- Wide detection range
ICON Plate-Based Cell Number
For cloning plate stage
- Rapid scanning
- High accuracy algorithm
- For 96 and 384 well plates
ICON Automated Viable Cell Counting
For expansion cell stage
- Trypan blue and AO/PI measurements
- From 1 to 24 counts per run
Solentim wins New Product Award at SLAS 2021
Solentim is delighted to have won a New Product Award from the Society for Laboratory Automation and Screening (SLAS), announced this week at SLAS Digital 2021.
ICON is powered by STUDIUS
- Manage: User management hierarchy including inbuilt user training course.
- HISTORYTREE™: Displays multiple data points from a clone’s history along a unique graphical timeline.
- Sort: Rapid filtering of per-cell data to characterize lead candidates.
- Report: Draws on system and service status within final report as evidence of quality process.
- Operates Continuous Audit Mode supporting requirements to achieve 21 CFR part 11 and EU Annex 11 compliance
Microscope Mode
High clarity microscopy for cell line development
ICON Microscope Mode offers cell line development scientists a convenient set of tools for viewing and the capture of cellular images. Ideally suited for quick review and confirmation of cell morphology and fluorescent expression of RFP and GFP signals.
