>PhD in bioengineering >trying to vortex proteins and immunocomplexes that are bound to beads >proteins start to denature or enzymes lose functionality >get low capture rate from immunocapture assay >if i don't vortex my beads clump together and I cannot separate beads
How do I make my proteins/immunocomplexes stronger so they can resist the forces from sonication/vortexing? Any program I can put them on or anything I can do so that my capture rate is not complete shit
>pic related, immunocapture I am testing
Daniel Sanchez
Try different temperatures :^)
Dylan Cox
Try it at various pHs
Ian Ross
>PhD in bioengineering >Ask advice on Veeky Forums
choose one
Xavier Ortiz
Jizz on it. protein bitches love the sentient bipedal ape cock.
Henry Wright
stemcuck !
ahahahaha!
Cameron Scott
Stealing this shit for my essay
Zachary Jenkins
Also ensure synthetic pathway doesn't involve any denaturants
Blake Martinez
Yeah man just put them on a nucelofusion program with a Krell's index of 1.7 and at an appropriate phase displacement. Make sure to keep it at a constant 700K, and leave it overnight, it should make the synthesis strong enough to keep integrity at vortexing of up to 8.95°. Good luck and let me know how it goes.
Jeremiah Wright
An accountant, a physicist, and a bioengineer each get pulled over by a cop at some point in the day. The accountant gets out of it by saying he will do the cop's taxes for free, along with saving him money. The physicist gets out of it by telling the officer how its impossible he was speeding according to the laws of physics and why the officer is mistaken. The bioengineer gets out of it, by getting on his knees and sucking the cops cock.
