Beckman Coulter Vi-CELL XR Automated Cell Viability Analyzer, 2 µm – 70 µm In Ramsey, MN, USA (CAT#: STEM-CAPO-0010-YJL)

Beckman Coulter Vi-CELL XR Automated Cell Viability Analyzer, 2 µm – 70 µm In Ramsey, MN, USA, model Vi-CELL XR, is manufactured by Beckman - Coulter general laboratory equipment.
The Vi-CELL provides an automatic and cost effective means to perform the trypan blue dye exclusion method for cell viability analysis. This data is essential to the decision making process for basic tissue culture cell passage and maintaining optimum culture conditions in bioreactors. Cell and tissue culture applications in life science research, including recombinant protein and biopharmaceutical production, require the accuracy, precision and automation available only in the Vi-CELL cell viability analyzer. Compared to a manual hemacytometer, the Beckman ViCell automates a formerly laborious process with extremely high accuracy and reliability.
The Vi-CELL allows users to load up to 10 samples at once for easy and automated cell counting.

Condition: Used
Liquid level capacity detection for accurate sampling: 2-6 µL for most tests
Software: Easy to use and train
Weight: 3,916 Lbs
Dimensions: 200 (W) x 45 (D) x 50 (H) inches

Powerful, Flexible Software
Bioprocess tracking, auto-sampler queue & control monitoring features
Real-time cellular imaging for data parameters not available with standard aperture cell counting methods
Provides results for percent viability, total cell & viable cell concentration and mean cell size
Operation
12-position auto sampler for walk-away sample analysis
Samples within 50 x 103 to 1 x 107 cells/mL range require no dilution
Customizable cell types for analyzing diverse cell species
Bioprocessing Applications
Key cell culture parameters to help you optimize and monitor the bioprocess
Results can be viewed easily on the screen or exported for off-line analysis
Through integration partners we offer optional automated online sample introduction for real-time cell analysis for improved bioprocess monitoring and control
Compliance and Validation
21 CFR Part 11 enabled with audit trail, electronic signature capability, secure sign-on, multiple user level permissions & administrative configuration tools
IQ/OQ

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