Category: NRG

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

Posted in NRG

Diffusion on shaker

I ran a few experiments using the stir cell on the shaker table. Diffusion occurs faster on the shaker, but more air bubbles form around the membrane, thus preventing further passage of rhodamine. The first experiment I ran was with

Posted in NRG

AFM Training

Yesterday, Chris, Dave, Graham and I were (exhaustively) trained on the Asylum AFM in Rick Waugh’s lab.  We had an overview of the basic features of the AFM and got some real data, as well. The top panel is a

Posted in NRG

W613 Discoloration

Given the mixed results of discoloration of RTPed samples from W613, which include no discoloration until 7 days (when the experiment was started within 2 hours of RTPing), and discoloration within 2 days (experiment started 8 days after RTP) I

Posted in NRG Tagged with: , ,

PDMS array on nitrocellulose

Below is an image of the PDMS array on the nitrocellulose membrane. I’m trying to create a stamp that can be applied to the NC membrane, before PDMS is poured on. The idea is that the stamp will be heavy

Posted in NRG

Time after RTP – Discoloration

Last week in lab meeting, someone wondered if there the time after RTP affects the rate of discoloration. To test this, I RTP’ed chips from w638 in Ar at 800C for 5 minutes. I then followed discoloration in DMEM+10%FBS in

Posted in NRG

Conditioned DMEM – re-try

Last week, I did a couple experiments based on a suggestion by Tom. The pH of DMEM starts out quite high and then buffers down into physiologic range after some time in the incubator. Tom surmised that a short exposure

Posted in NRG

Diffusion-based Chemotaxis Chamber

Hi all, For quite some times we have been trying to design a diffusion-based chemotaxis chamber that operates under an environment of 37 degrees Celsius in temperature. One main obstacle that we face is the evaporation of the 2 uL

Posted in NRG

Desalting BSA: Blank pnc-Si and Mini-Dialysis Units

The ultimate experimental goal of the desalting project is the removal of salts from a salt/protein solution while fractionating certain sized proteins with maximum protein retention and recovery.Thus far we have characterized the flux of salt through our membranes which

Posted in NRG Tagged with: ,

UV Ozone bonding of PDMS to glass, Si, and pnc-Si

Hi all, After experimenting with UV ozone bonding of PDMS to glass, Si, and pnc-Si for the past few weeks with Mike, we have reached the following conclusions: 1. The bonding of PDMS to glass is always stronger than the

Posted in NRG
0
    0
    Your Cart
    Your cart is emptyReturn to Shop