Dear WiseOnes,
I wonder if you would enlighten me! I am attempting to undertake
proteomics in a model of skin scarring. Has anyone undertaken skin
proteomics before aside from the in-depth work carried out by Celis'
group in Denmark? How have samples been physically disrupted? Has
any sample buffer composition shown to be preferential?
Any pointers would be appreciated.
Many thanks,
Dr. Jon Pleat
Stoke Mandeville Hospital,
United Kingdom.
jonathon.pleat at talk21.com