Webinars

An overview

In this webinar, we will discuss how Chirascan Circular Dichroism Spectrometers from Applied Photophysics help researchers gain insights in protein secondary and tertiary structure studies. We will focus on the innovations which make Chirascan more sensitive, more reproducible and more versatile.

Using circular dichroism to quantitatively compare the higher order structure of protein biologics

Speed and precision: fast kinetics studies with the Stopped-Flow spectrometer

In this webinar, we present our results showing regulation of a prototypical ion channel, KcsA, first by changes in bilayer thickness and second by a set of drugs that vary in their bilayer modifying potency as sensed by gramicidin channels.

In this webinar, we present our results showing regulation of a prototypical ion channel, KcsA, first by changes in bilayer thickness and second by a set of drugs that vary in their bilayer modifying potency as sensed by gramicidin channels.

Small molecules, such as drugs, interact with membrane proteins directly and will also modify the lipid bilayer. This concept can be exploited to give valuable insight into the cytotoxicity of vast libraries of compounds. Here’s an opportunity to attend a two-part series of live webinars discussing the concept of bilayer modification by small molecules and how you can utilise it to characterise the potency of potential toxins. The two 30-minute sessions will include time for questions on the regulation of membrane protein function.

Small molecules, such as drugs, interact with membrane proteins directly and will also modify the lipid bilayer. This concept can be exploited to give valuable insight into the cytotoxicity of vast libraries of compounds. Here’s an opportunity to attend a two-part series of live webinars discussing the concept of bilayer modification by small molecules and how you can utilize it to characterize the potency of potential toxins

In this webinar, our application scientist, Dr. Alastair Davy, will demonstrate the workflow for measuring the Gibbs Free Energy of proteins, using the SUPR-CM fluorescence plate reader.

A look at the SUPR-CM workflow and how the system can enhance the antibody engineering process

The SUPR-DSF delivers next level differential scanning fluorimetry by simplifying sample preparation and analysis of protein stability into a single microplate. Utilising precision optical components to deliver the highest sensitivity, intrinsic fluorescence of proteins and full spectrum detection, both thermal ramping and isothermal chemical denaturation experiments can be easily run in 384-well microplates.

This is a quick overview of Protein Stable's SUPR-CM and SUPR-DSF instruments.