DNA/mRNA characterization
Protein-protein interactions
Antibody aggregation
Membrane protein analytics
Antibody Aggregation
Join us for a special two-day workshop at Vanderbilt University Aug. 26 and Aug. 27 to learn about mass photometry and gain insights in to assessing sample heterogeneity, aggregation, or binding interactions without wasting precious material.
Refeyn’s TwoMP mass photometer offers a powerful, label-free solution for rapidly analyzing biomolecular mass, purity, and interactions in their native state with as little as a single microliter of sample.
Day 1 Session
Vanderbilt University
Location: MRB3 room 3131
Date and Time: Aug. 26 | 3pm – 4pm (CST)
Austin Graves, PhD, Senior Field Applications Scientist at Refeyn
Day 1 Session Summary
On Day 1, join us live or via Teams at Vanderbilt University for an exclusive Mass Photometry Workshop hosted by Refeyn. Led by Austin Graves, PhD, Senior Field Applications Scientist, this event offers a unique opportunity to explore the transformative power of mass photometry in biomolecular characterization.
Day 2 Session
Vanderbilt University
Location: MRB3 room 5132
Date and Time: Aug. 27 | 10am – 4pm (CST)
Sara Wilson, Senior Technical Sales Specialist at Refeyn
Day 2 Session Summary
On Day 2, step into the lab for a focused, small-group session on the TwoMP mass photometer. You’ll gain practical, expert-led training on instrument setup, sample handling, and data interpretation—giving you the confidence to bring mass photometry into your own workflows.
Want to see how TwoMP performs with your real-world samples? Bring them along and experience firsthand how this technology delivers precise, label-free analysis in minutes (see sample submission details below).
Please note: Due to lab space limitations, sessions will be held in small groups of 3–4 participants. Additional information regarding group assignments will be shared on Tuesday, August 26.
Sample requirements
Sample Limit:
1-2 samples per person
Mass Range:
30 kDa to 5 MDa
Sample Concentration:
Ideally, stock solutions should be at a concentration of 1 μM or higher (for proteins & biomolecules) or 500 ng/ μL or higher (for nucleic acids) as prior to measurement samples will be diluted to 5-20 nM (proteins) or 20-50 ng (nucleic acids).
Sample volume:
≥ 10 µL for stock solutions, but the volume per measurement will be 10-20 µL
Buffer Requirements:
Your preferred buffer can be used for the measurement of your samples. Please provide us with 5 mL of your buffer for dilution purposes, equilibrated to room temperature (RT). In the event your buffer contains any of the following “additives” we kindly ask you to have buffer without these additions present (also 5 mL):
- Urea or guanidium hydrochloride (Gnd-HCl)
- Glycerol, sucrose, or other sugars (only if above 10 %)
- Detergents
- Inorganic solvents (e.g. DMSO only if above 5-10 %)
Registrations closed
Event Host & Contact Information
This workshop is hosted by the Vanderbilt Center for Structural Biology. For questions, please contact Heather Kroh, PhD, Scientific Director and Core Manager (Biophysical Instruments), at heather.k.kroh@vanderbilt.edu.