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描述 Nanosep centrifugal devices are formed out of two components, a filtrate receiver tube and a sample reservoir containing the membrane. These component parts are constructed from low protein binding polypropylene that also offers chemical compatibility for aggressive solvents. Instead of using O-rings or adhesives that could add extractables or bind precious biomolecules the product is constructed using an ultrasonic welding technique. These centrifugal devices are very simple to use. The sample to be processed is pipetted into the upper reservoir of the device. The device is placed into the appropriate centrifuge (taking care that the rotor is balanced) and spun. Filtrate can be recovered by removing the lower reservoir of the device and using a pipette or pipette tip to remove the liquid. Nanosep centrifugal devices can be used with sample volumes of up to 500 µL, and fit in standard centrifuge rotors that accept 1.5 mL tubes. Ensures rapid processing of samples Low protein binding Omega membrane for ultrafiltration applications A wide range of MWCOs, color coded for easy identification Constructed of low-binding polypropylene Ultrasonically welded seals prevent bypass or seal failure Fits standard centrifuge rotors that accept 1.5 mL tubes Nanosep centrifugal devices with Omega membranes can be used in a number of ultrafiltration applications including; the concentration, purification, and desalting of peptides, proteins, oligonucleotides, DNA, and RNA. They can also be used in the isolation of DNA from agarose gel slices, and to separate proteins, oligonucleotides, and RNA from acrylamide gels. Omega ultrafiltration membranes are manufactured from low protein binding modified polyethersulfone minimizing the possibility of sample losses due to non-specific binding. A wide selection of molecular weight cut-off (MWCO) options are available and devices are color coded for easy membrane selection. Pall supply users with a Nanosep concentration selection guide. The guide allows users to concentrate a sample to the concentration of their choice. This is achieved by selecting a volume of buffer solution to place in the device filtrate receiver tube prior to sample processing. The total volume of liquid in the device determines the final retentate volume. 类型 自旋装置 用途 样品浓度 脱盐 缓冲液更换
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文献和实验Genotyping using Affymetrix arrays
. The hybridization solution was heated to 95 °C for 10 minutes then placed on ice. After warming to 48 °C for 2 minutes, 200 µL of the hybridization solution is injected into cartridges housing the oligonucleotide arrays (Affymetrix GeneChip® 100K Mapping Set: 50
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Geno typing using Affymetrix arrays
. After warming to 48 °C for 2 minutes, 200 µL of the hybridization solution is injected into cartridges housing the oligonucleotide arrays (Affymetrix GeneChip® 100K Mapping Set: 50K Array Xba 240 and 50K Array Hind 240). Hybridizations are carried out at 48 °C
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