One of the major goals of my work with capturing exosomes is to show that our purified population is less contaminated with protein than exosomes purified by ultracentrifugation. This is important because the protein (and all the other junk floating in plasma such as cfDNA) can cause problems with identification and characterization of the exosomes….
Some of my recent cell culture work on Microporous MgF2 windows have shown vacancies in the cultured monolayer after fixation and staining. We should see a contiguous layer. To better understand my fixation, I seeded and cultured P10 RPE-19 cells at a high density on a coverglass and in a polystyrene dish for a week….
Introduction Endothelial cell detachment under flow on porous substrates has been a concern in our sepsis research since I began my work in the lab, and some time before that as well. As we plan on moving to microfluidic models that incorporate larger pore substrates and physiological shear stresses for extended periods of time, it…
As we run our CCD (Central Composite Design for Optimizing SERS Substrates, SERS Measurements on 150C, 250C, 350C 1236 npMgF2), we have also been gathering TEM/SEM structural information about pore distributions and MgF2 grain structure. This post contains images about materials and compares them to information we know about wafer 1085, one of our original MgF2…
There is no excerpt because this is a protected post.
This post includes some optical and SEM micrographs of a SiO2 membrane patterned by nansosphere lithography using 300 nm polystyrene beads. An SU-8 microgrid was deposited on top and the membrane was released by dissolving a bottom layer of ZnO. After the release, the membrane is rinsed in water and transferred to a clean substrate….
I am attempting to manufacture a range of npMgF2 thicknesses as demonstrated in my recent CCD post. Yesterday, I undershot my thicknesses substantially, I believe because of construction vibrations in the building. However, this results in some of the thinnest npMgF2 structure I have ever been able to image. I was targeting 15 nm, but…
In my previous blog, I alluded to the issues I was facing in achieving successful migration of neutrophils through the basement membrane into the collagen gels. I am successfully able to achieve transendothelial migration, but migration beyond the endothelial basement membrane is still not achievable. After a lot of thinking, I realized that this, in…
I have three monolith experiments to report, one of which was successful. In all three cases, I was able to make a pore, though it took about 5 times longer than it would have for the NPN-tented chips. This is likely a consequence of the reduced exposed membrane area in the monolith case, which is…
Now that we have a number of ways to quantify the nanostructure of different npMgF2/npAu film stacks, we can begin an optimization experiment for which combination of factors will be useful to us. To explore the space of outcomes, we have a set of Factors at a certain number of Levels. These produce a set…