I have a primer that add HisTag (direct w/o linker) to the C terminus of HCV Core (191aa.)
I am expressing this gene as a recombinant baculovirus in Insect cells and I want to detect by western (Anti-HIS) and then purify by Ni-NTA.
I skeptical about the fact that maybe the C-terminus His Tag will be cleaved due to the SPP.
and Also if not will the folding of the Core mask the His tag?