Category: NRG

Sepcon-transwell discoloration II

I repeated a previous experiment but this time I used samples (no RTP) from W685 in oven @ 37C in DMEM(-FBS). Four type of samples (blank chip with no slits, chip with both intact membranes, chip with one intact membrane

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Porosity vs Discoloration I

We have known, W683: no visible pores; W684: very few pores; W685: usual porosity. After Vlassak’s view on discoloration, I took samples from above wafers to check if any difference in discoloration can be seen as they have different porosities.

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HUVEC 'proliferation' in Sepcons

Last week when I reported no membrane breakage after a week of HUVEC culture, I showed a phase micrograph on day 7.  This week I tracked the HUVECs a bit more closely with the microscope. This is 10X, HUVEC P5,

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Pressurized rerun with w670

Previous Post The previous w670 pressurized flow gels showed one trial with a lower cutoff than w673 and one trial with nothing passing through.  This experiment was run for 40 min and in each case I saw only 0-3 uL

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1st HUVEC TEER data

I recently completed some experiments with the Endohm system, which measures transendothelial electrical resistance (TEER).  I seeded either 16.25k or 32.5k HUVECs (P5) on commercial polycarbonate (PC) or polyester (PE) transwells and on pnc-Si in the transwell format.  I then

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Discoloration – Sepcon pieces

Since we’ve been noticing slower discoloration in the Sepcon format, I looked at the 2 components of Sepcons – the plastic and the O-ring. Specifically, I cut pieces from w622 and incubated them in FBS-DMEM/F12 either alone, with the Sepcon

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Sepcon-transwell discoloration study I

In an earlier post we saw that intact membrane sample discolored slower than the broken one. To establish this, a study using four types of samples from #702 (blank chip with no slits, chip with both intact membranes, chip with

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Bead Assay in Sepcon

I carried out the bead assay to monitor membrane integrity in Sepcon format. The sample (no RTP) was taken from #703 and put in DMEM(-FBS) @ RT with membrane side facing up. 15um polystyrene beads were allowed to settle on

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Cell viability – XTT

XTT is a colorimetric assay for measuring cell viability.  Supposedly, it gets taken up by cells and is reduced by mitochondrial activity intracellularly into water-soluble orange formazan crystals.  The readout is the absorbance of these orange crystals. I used XTT

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Discoloration CVC vs. AJA Tool

Based on Barrett’s array set up for discoloration, I set up an array experiment to check the discoloration effects between the new and old system ( 2e-7,AJA vs the older 7e-7 CVC ). The wafers from each had a bit

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