This is a very basic question, and I would be very happy, if you could share some of your experience with me. In my hands, GST by itself is always a dimeric protein (from size exclusion profiles), and the buffer conditions don't really seem to affect the dimer formation. I always assumed, that also the GST-fused proteins were dimers, but I found some papers that managed to show monomeric GST-fused proteins. What do you reckon?

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