by
danko » Sun Dec 07, 2008 5:25 pm
HPLCgroupEurope,
The stationary phase is not the only parameter that can be varied in order to achieve a purification or analytical separation for that matter - in fact, far from it. So, mobile phase, temperature, flow rate etc. can be the tools you should look at. And only in the context of a particular peptide/protein (they all have different properties)
Generally, if your project is; finding a single stationary phase and standard chromatographic conditions for purification and analysis of all thinkable peptides, I’ll have to disappoint you – you’ll fail.
I was (unwillingly) involved in such a project, recently. And even though I predicted the outcome, we had to go through the project, which of course ended up with a useless collection of different stationary phases, mobile phase compositions and other parameters. The situation now is: Just going through all this information, takes longer time than developing a new method from scratch - because none of all this parameters can be directly applied on two different peptides/proteins.
All these projects aim at a potential elimination of the need for knowledge and professionalism and this is the main problem with this conception.
Best Regards and good luck.