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查看更多产品信息 Rapid Equilibrium Dialysis (RED) Inserts and Plates - FAQs (90088, 90087, 90112, 91012, 90004, 90006, 90005, 99006, 89809, 90085, 89812, 89811, 90007, 89810, 90006B)
19 个常见问题解答
Each sample requires two chambers for equilibrium dialysis to take place (96/2 = 48).
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Yes, as most assays are performed at physiological temperature (37.5 degrees C).
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No. It will not affect the equilibrium.
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Once samples are loaded into the PTFE plate it should be placed on a shaking device. With an orbital shaker 100 rpm works well. For an up and down shaker, 20 rpm is sufficient.
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A final concentration of 1% DMSO is acceptable and will not affect the study. While DMF has not been tested, it is expected that DMF should be similar to DMSO in terms of use.
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No. After use, rinse the PTFE plate in 20% ethanol in water and rinse with ultrapure water at least two times. No radioactivity will remain after these rinses.
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No, these are designed for a single use, as plasma is sticky and cannot be removed from the unit. The PTFE plate is designed for multiple uses.
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The lowest validated volume for the RED Device sample chamber is 50 µl of plasma.
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Plasma samples from human, mouse and rat. For toxicology studies, monkey is also typically tested. Typically pooled plasma samples purchased from commercial vendors are used, although researchers could test the differences in plasma from various physiological states using the RED Devices.
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The container for the device is PTFE and the insert is made of high density polyethylene (HDPE) and are highly hydrophobic. The regenerated cellulose membrane is a standard material for commercial dialysis devices. A recovery study shows a consistency of 85% recovery of high and low protein binding compounds. This result is indicative of minimal non-specific binding.
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Volume shift in the plasma is unusual due to how quickly equilibrium can be reached with the RED Device. If much longer incubation times are used, there can be an increase in the volume of the plasma. However, the ligand will still reach equilibrium, having free ligand at the same concentration on both sides of the membrane.
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The difference in liquid volume is to maintain the same level (height) between the two chambers. The equilibrium constant depends only on the concentration of the ligand, not the volume.
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In most cases 4 hours is sufficient to reach equilibrium. This is due to the high surface area to volume ratio for the membrane (7.4:1).
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The units do not undergo a sterilization procedure nor are they tested for endotoxin content.
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No. The inserts can be used directly out of the package, no presoaking or rinsing of the membrane is needed.
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The nominal MWCO is 6,000-8,000 Daltons as specified by the manufacturer.
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Regenerated cellulose with a low glycerol content as a humectant.
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Please view our selection table to choose the right dialysis device for your experiment - https://www.thermofisher.com/us/en/home/life-science/protein-biology/protein-purification-isolation/protein-dialysis-desalting-concentration/dialysis-products.html.
Dialysis is the separation of small and large molecules in a solution by selective diffusion through a semi-permeable membrane. It is generally used for larger sample volumes, and can take hours to overnight for complete dialysis.