3D Printable Capture Device Design
NOTE: Apologies for the formatting on this post. I seem to be unable to add blank lines for some reason.
NOTE: Apologies for the formatting on this post. I seem to be unable to add blank lines for some reason.
Introduction Motivation: We want to assess if the bladder cancer cell line T24 would influence the baseline characteristics of bladder epithelial cells (BdEC, a.k.a. ATCC® PCS-420-010™) when the two cell types are cultured together. Ultimately, we are interested if the T24 induces BdEC malignancy (turning the normal epithelial cells cancerous). Goal: Investigate if BdEC monolayer will break…
This previous post contrasted how gold could be separated by pressure in deionized water, but not by diffusion (w199). I checked up on that diffusion sample again after 6 days, and while the retentate had mostly evaporated, there was no gold within the remaining filtrate. As you may recall, there has been some discrepency with…
Introduction & Background Parylene is a polymer stemming from the chemical-vapor-deposited poly(p-xylylene) group. This polymer treatment is applied as a gas which allows complete and uniform coatings of substrates with even nanoscale features. Parylene treatment is widely used as it offers a chemically and biologically inert layer with excellent electrical properties, and additionally acts as…
SET-UP Syringe pump: 5 mL of 7.6-nmol/100µL, 5.6 µL/min pump rate. Single Channel dialyser, 10 mm long, 0.5 mm wide, 0.3 mm high in stirred beaker of DI water Fraction Collector programed to rotate every 30 min. Set up in refrigerator, 40˚C. Figure 1: Long term dialysis clearance set up in refrigerator. Syringe pump, stirred…
Separations were performed at 2 different salt concentrations with equal volume filtrate and retentate (to avoid dilution problem). Separation time was 40hrs rather than the usual 24. The lower salt concentration run has a lower cutoff – which is just like what we see in the DNA separations. Remember though that proteins have different charges…
Over the last couple of weeks, I’ve been doing confocal fluorescence microscopy over at the Med Ctr. I was hoping this tool would clean up some of the background fluorescence in my immunofluorescent images. More importantly, the confocal can take ‘slices’ of images in the z-plane and stack them on top of each other to…