Adapt your lab microplate reader for bacterial endotoxin testing
3 Apr 2025
Join Timothy Francis, from Fujifilm, as he explores the adaptation of microplate readers for bacterial endotoxin testing. This presentation delves into key techniques, including gel clot, turbidimetric, and chromogenic methods, with a special focus on the importance of kinetic measurement approaches. Learn how SoftMax Pro Software ensures compliance with GLP and GMP standards and discover a step-by-step protocol for the Kinetic Turbidimetric assay.
About the company
Molecular Devices®
Molecular Devices is one of the world’s leading providers of high-performance bioanalytical measurement systems, software and consumables for life science research, pharmaceutical and biotherapeutic development. Included within a broad product portfolio are platforms for high-throughput screening, genomic and cellular analysis, colony selection and microplate detection. These leading-edge products enable scientists to improve productivity and effectiveness, ultimately accelerating research and the discovery of new therapeutics. Molecular Devices is committed to the continual development of innovative solutions for life science applications. The company is headquartered in Silicon Valley, California, with offices around the globe. For more information, please visit www.moleculardevices.com.
General Inquiry - USA & Canada: +1 800-635-5577 General Inquiry - Europe: 00800 665 32860 Sales +1 877-589-2214 Support +1 800 635 5577
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SoftMax® Pro GxP Software
Molecular Devices®Meet FDA guidelines in GMP/GLP labs with complete validation tools
SoftMax® Pro Microplate Data Acquisition & Analysis Software
Molecular Devices®SoftMax ® Pro Software is designed to provide the simplicity, flexibility and power required for advanced data analysis. It provides ready-to-run protocols, analysis algorithms, and 21 different curve fit options. Every step has been optimized for data acquired from a Molecular Devices microplate reader or data imported from another source to simplify analysis and reporting. FDA 21 CFR Part 11 compliance tools are available for regulated laboratories providing end-to-end chain of custody.
