On Wednesday we ran several separations using both the EA and PEG treated membranes. The treatment process had damaged many of the chips. Of the 10 treated 10nm PEG chips, 2 survived. Of the 10 treated 15nm PEG chips,…
On Wednesday we ran several separations using both the EA and PEG treated membranes. The treatment process had damaged many of the chips. Of the 10 treated 10nm PEG chips, 2 survived. Of the 10 treated 15nm PEG chips,…
In a previous post, we showed that both Cytochrome C and BSA at concentrations of ~1mg/mL through 20nm cutoff Sepcons with about the same filtrate concentration (~60% of the feed concentration). Yesterday (1/14/13) we repeated these experiments with 10 and 15nm…
Before the fresh Cytochrome C arrived, I ran two samples. The first sample was our old Cytochrome C in 0.3mM sodium phosphate buffer at a concentration of ~1mg/mL. I passed it through the 20nm cutoff 3rd generation Sepcons by spinning it…
Recall that we’ve been having a great deal of trouble following the free ligand during our separations of the Bioconjugated Barcikowski particles, and that this trouble also means we can’t see the ligand after centrifuging the pure sample. In the…
On Friday(which was a great day for science). I ran a series of 5 passes of the bioconjugated gold nanoparticles through 30nm cutoff Gen 3 Sepcons. If you’ll remember, the Barcikowski lab wants the free ligand separated out from the…
Nanoparticles Inventory – taken by Karl on 11/2/12. All these particles can be found in the refrigerator. Manufacturer size type amount (approx) expiration date fluorescence (if applicable) BBI 5nm gold colloid 3mL Jan-10 BBI 5nm gold colloid 6mL Aug-11 BBI…
The Barcikowski lab sent us generous amounts of three different samples – gold, platinum, and bioconjugated gold. Each of the samples was created via laser ablation, resulting in fairly polydisperse (4-50nm diameter) nanoparticles for the pure metal and significantly less…
Because the Barcikowski lab intends to use the nanoparticles they sent us, relatively high yields are necessary for any step that cleans them up. This is unfortunate, because in every single separation that we’ve done (with one exception mentioned further…
The Barcikowski samples, sent from Germany a month ago, continue to be a fecund source of inconsistant data. Using the DLS to monitor several filtrations has resulted in a series of baffling results that I think I’ve finally begun to…