Evan Eichler estimates that around 5% ~ 400 specific loci on the genome will require alternatives in the ref genome to capture diversity 21 hours ago
Lincoln Stein called the effort to finish the HGP ref genome 'more of an abstract exercise than 1 that's going to have a practical impact' 21 hours ago
The Warda-Han-Proteomics saga continues and finds its way to the show/entertainment business. We’ve already listened to Han, now it’s time for Warda to speak, which he did in an email to James Randerson over at the Guardian Science blog, which makes think (indeed ‘rethink’ as W suggests) that the Warda-Han pair is probably the Laurel and Hardy of the science showbiz.
Have you ever wanted to isolate subcellular components from molecules to organelles with the old but ever improving ultracentrifuge method but were unable to figure out a correct protocol as the basics were not that clear?
To get an optimal protocol you have to take account the biological entity and pellet you want, the maximum volume input you need, the rotor and pathlength available in the lab and the time you have for all this.
Lately I’ve learnt the basics of ultracentrifugation from Richard Sicard (Thermo Scientific) who was nice enough to send me an excellent educational material called Ultracentrifugation: Basic Training from Thermo Fisher Scientific also giving me the permission to share it. I’ve chosen 14 slides. If you need a bigger resolution (especially on slide 2, 4), go to the Slideshare version and click full.