Author: Jessica Snyder

Track Etched EO

I sealed track etched membranes into the usual E-Cell setup. Here’s a chart with the calculated flow rates: I’m not sure why the 50nm sample was so much higher. Maybe there’s a difference in porosity? Also this is only the

Posted in NRG

Effect of PES Cutoff on "Electro-osmosis" Rate

We have two cutoffs for the Millipore Biomax PES membranes: 50kD and 30kD.  I tested the “EO” rates for both of these membranes and plotted them in this figure with standard deviations (3 trials  of 50kD and 4 of 30kD).

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w677 Separation

Here are the results of a protein ladder separation with w677.  If you recall, 677 is the 200um wafer that did not fit into the SepCons but had very few pinholes. S = Standards Ladder, C = Protein solution that

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Effect of Active Area on Electroosmosis

Does more active area mean more fluid transported by electroosmosis? To test this I found an ancient wafer (w13) that had different active area geometries. Can someone check and make sure I got these right: Long slit – .1 x

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Negative Adsorption Assay Retry

This is a retrial of the previously outline negative adsorption assay.  I was a little more careful with cuvettes this time around (there are very significant differences in the plastic cuvettes) and I spread out the same amount of solution

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Electro-osmosis update

Here’s some data from my electrophoretic trials with polymer membranes. On this chart, both PES and Cellulose fall on the same line.  In my last post I said that PES membranes didn’t seem to pass water, although I found that

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Adsorption Negative Assay

If protein is adsorbing to a surface, it’s leaving the solution.  We can indirectly measure how much protein is leaving the solution, and that may tell us something about how much these surfaces are adsorobing. For my first attempt, I

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Electro-osmosis with polymeric membranes

The Burns-Zidney paper uses streaming potential to measure the zeta potential of polymeric membranes.  This means that polymeric membranes should also be capable of performing electro-osmosis, essentially the opposite of streaming potential.  For more on this, I have a knowledge

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Electrophoretic (Stir) Cell Update

I used the source meter that Chris brought over and tested the voltage at points across the chamber. I set up the system with 1x PBS at 15V (~10mA) with a pinholed membrane. I tested the voltage drop at the

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Upping the ante

I guess we weren’t sure if I was actually drawing rhodamine back through the membrane or just bleaching it. So I made a new apparatus which consisted of a sawed off sepcon mounted on a slide with channels etched into

Posted in NRG
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