• Cell Labeling on Si

    Below is an image of HUVEC grown on RTP treated W303 for 72 hours. The cells were seeded at high density and therefore reached confluence prior to day 3. The first row shows the membrane area of the sample; the membrane is not intact. The second row shows the edge of the sample. Live and…

  • Wafer 398

    Wafer 398 was deposited on 2/14/2008 but just etched yesterday in the new cell (it’s a beauty esp. when you compare it to the old one). I’ve etched several wafers now in the new cell and none of the membranes show signs of cigarette burns or tears. Good news in regards to the copper contamination…

  • Wafer 415-T

    Wafer 415-T has been delivered to the lab. It was processed with TEOS and annealed at 950 C. There are a few usable samples, especially along the edge of the wafer. Pinhole density increases as you move towards the center. The uniformity across the wafer is good. From left to right, top to bottom: (0,1)…

  • Gold Trials

    Most recently I’ve been working with colloidal gold nanoparticles (referred to as AuNP from here on). We chose to use AuNP for separations because it is an ideal hard sphere particle, unlike a floppy protein. We thought we could achieve more information about the cutoffs or the sieving characteristics of the membrane by using such…

  • HUVEC on pncSi

    In order from left to right: 1) t=0, huvec on pncSi, in EGM (10% FBS) 2) t=24 hrs (cells reach confluence) 3) DIC after staining 4) FITC (live cells) 5) Rhodamine (dead cells) Its good to see the cells reach confluence and the membranes intact at the same time! There is a decrease in number…