If your protein elutes very late, that means it's binding to the column matrix (so all estimates of size go into the trash). Check to see that the ionic strength of buffer is reasonable (equivalent to, say, 150 mM NaCl). If so, then the only solution is to go to a different matrix type. Pat
On 20 Jun 2013, at 3:09 PM, Zhang, Zhen wrote: > Dear all, > > I just observed a puzzling phenomenon when purifying a refolded protein with > size exclusion chromatography. The protein was solubilized by 8M Urea and > refolded by dialysis against 500mM Arginine in PBS. The protein is 40KDal and > is expected to be a trimer. The puzzling part is the protein after refolding > always eluted at 18ml from the superdex S200 column (10/300), which is > calculated to be 5KDal by standard. However, the fractions appear to be at > 40KDal with SDS PAGE and the protein is functional in term of in vitro > binding to the protein-specific monoclonal antibody. I could not explain the > observation and I am wondering if anyone has the similar experience or has an > opinion on this. Any comments are welcome. > > Thanks. > > Zhen > > > The information in this e-mail is intended only for the person to whom it is > addressed. If you believe this e-mail was sent to you in error and the e-mail > contains patient information, please contact the Partners Compliance HelpLine > at > http://www.partners.org/complianceline . If the e-mail was sent to you in > error > but does not contain patient information, please contact the sender and > properly > dispose of the e-mail.
