Author: Jessica Snyder

Recent Discoloration in other Projects

Bernhard Group: Discoloration was observed during DNA separation experiments.  Further study led to these results: No discoloration observed with low pH buffered NaCl. Discoloration with high pH buffered NaCl. Worried that Cl was the culprit, sodium acetate was tested.  Discoloration

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8 hour diffusion

Because of the recent discoloration problems I observed with 24 hour diffusion using w670 and 673, I decided to try a shorter time point. 673 had a couple more samples to spare, so I tried an 8 hour diffusion experiment. 

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Pressurized Movable Cutoffs

While wafers 670 and 673 did not hold up to diffusion experiments, they were strong enough to perform pressurized separations using the pressure cell.  Each experiment lasted for 40min, although the average flow was only about 5ul for this duration.

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Water Permeability Statistics

I’ve processed all the images used in the water permeability studies and found the following statistics from these images: Mean Diameter Mean Area Median Diameter Median Area Porosity Area Weighted Diameter 90th percentile Diameter I calculated the theoretical water permeability

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Original Contact Angle Study

This is the original contact angle study performed using the DeLouise Lab’s Rame-Hart contact angle measurement tool.   The entire study was performed on 8/1/06-8/10/06. Observations: Contact angles of non-plasma oxidized samples start ~60 degrees and increase over about 10 hrs

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Diffusion Separations w/ 670, 673

Wafers 670 and 673 were made to have different cutoffs. I set up diffusion experiments with two chips from each wafer using protein standards. However after removing samples after 24 hours I noticed that both chips from w670 had fully

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Negative Assay Follow Up

In yesterday’s post I showed that I was able to obtain good negative adsorption assay results, but there was one major problem. The cellulose and PES actually had higher protein concentrations after the assay. I suggested this was because they

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Negative Adsorption Assay

The Tecan Nanoquant plate is amazing.  For those of you who are unaware, we were able to demo a quartz plate that enabled absorbance measurements with only 2ul drops.  It took a little bit for me to figure it out,

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Pore Processing

Here is the current method that I am following to find the pore statistics: 1. Select the highest threshold that you can still close with disk of 3 2. Hit majority 3. Close w/ 3 4. — Try open w/

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Negative Adsorption Assay

This is a retrial of the negative adsorption assay using the Tecan spec/fluorimeter that we have been demo-ing. To perform this assay, I am applying a known concentration to the surface I want to test. After an hour I remove

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