My 6th week of summer research was really busy.
Coming to a realization that fitting method (model) I created last week was not
a good fit to other nanocomposite film, I decided to refine the fitting method,
especially the fitting method for gold nanorod layer. What I was trying to do
was fitting the polystyrene and gold nanorod layer separately. Hence, I first
fitted the polystyrene layer and measured its thickness right after the PS
solution was spin coated on the glass substrate. Then, I dropcasted gold
nanorod solution directly onto the glass substrate to create a separate gold
nanorod layer. Using the ellipsometer, I, again, recorded the thickness and created
a fitting method. Without the influence of variables from polystyrene layer, the
fitting process for gold nanorod layer will be easier and more precise. Following
that, I combined the two separate fitting methods together to create a complete
fitting method for PS film embedded with nanorod. In addition to refine the
fitting method, I also annealed two sample films at 140 Celsius for 3.5 hours and
another one sample at 140 Celsius for 12 hours. Performing the AFM imaging to
the annealed films, I can apparently see that most of the nanorods went down in
the PS layer, a small amount of nanorods, however, were still at the surface
because their contact angle problems. For next week, I am going to apply SEM to
sample films to characterize the orientation of nanorods.
We started off our week with a congratulatory acai bowl trip to celebrate Preston’s acceptance into a training grant program. Acai bowls in California top Playa Bowls (no question about it). From what I can tell, its a pretty huge honor to be recognized by this grant, but he’s really humble about it. On Monday, Preston and I decided that testing antibodies that have never been tested on prostate epithelial cells before would be a good objective for my first Western blot on my own. We needed to probe for ASCT2, a glutamine transporter, and GLS in order to determine if their corresponding antibodies are functional. Antibodies are crucial for Western blots because they bind to the protein of interest (POI), allowing for us to qualify its expression after imaging. As such, Preston wanted to make sure they worked by probing for ASCT2 and GLS on three different cell lines. Cell lines are commercially purchased human cells that have been immortalized (modified to grow indefinitely) by telome...
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