Inclusion bodies purification is very easy and can be performed using very common reagents. You can find a lot of protocols in google.
Inclusion bodies are almost impossible to reconstitute in buffer without chaotropic agent or strong detergents. If you sonicate your cells in simple PBS or PBS/detergent inclusion bodies will surely stay in nonsoluble fraction.
Here you have a protocol for IB purification: https://labs.fhcrc.org/strong/StrongLabRefoldingProtocol.pdf
Inclusion bodies purification is very easy and can be performed using very common reagents. You can find a lot of protocols in google.
Inclusion bodies are almost impossible to reconstitute in buffer without chaotropic agent or strong detergents. If you sonicate your cells in simple PBS or PBS/detergent inclusion bodies will surely stay in nonsoluble fraction.
Here you have a protocol for IB purification: https://labs.fhcrc.org/strong/StrongLabRefoldingProtocol.pdf