There are a lot of increasingly complex ways to measure proteomics in blood. You can use 100 different nanoparticles or mix in aptamers or use double antibody arrays - all things that can be easily translated to the clinic as long as you're willing to pay
for your next blood test!
So...what if you took a step back? Maybe 10? And used actual clinically available material? And then what if you fully embraced heresy and used HPLC methods that someone in a clinic would actually be successful doing?
Sounds like science fiction? If so, you should check this out.
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