Pantalones
New member
I'm very curious regarding the process done in laboratories to identify and count various blood markers (hormones, vitamins, anti-bodies, etc.) I understand most of this equipment uses mass spectometry, of which I understand partially. I understand that the atoms are ionized by knocking off one or more electrons to give a positive ion, and that those ions are then accelerated to add kinetic energy. The basic premise of this process seems to be the deflection, that in which these ions are deflected according to their individual masses, and then charted based on this deflection..and it is this that then gives you what we know the substance to be. What I am confused on is how the detector can possible pick up on the location of each ion in a compound such as hormones or proteins, which often tend to be folded and such. That would mean two of the ions may overlap, and that would give a confusing reading. To me this mass spectometry just doesn't seem very accurate. I know I am w!
rong, but I would like someone to explain this to me. Also, if you could, I'm interested in learning on how such physiologic markers are discovered anyway, or in other words, how do we actually first know what these hormones, proteins, and globulins look like anyway? I feel like they could easily just bullshit people lol
rong, but I would like someone to explain this to me. Also, if you could, I'm interested in learning on how such physiologic markers are discovered anyway, or in other words, how do we actually first know what these hormones, proteins, and globulins look like anyway? I feel like they could easily just bullshit people lol