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Percll-密度梯度离心教程
Percoll density gradient centrifugation;Outline;For biological particles, the ideal gradient medium has been described as one having the following characteristics:
? covers a sufficient density range for isopycnic banding of all biological particles of interest
? possesses physiological ionic strength and pH
? is iso-osmotic throughout the gradient
? has low viscosity
? is non-toxic
? will not penetrate biological membranes
? is supplied sterile and is resterilizable
? will form self-generated gradients by centrifugation at moderate g-forces
? is compatible with biological materials
? is easily removed from purified materials
? does not affect assay procedures
? will not quench radioactive assays;Principles of density gradient centrifugation;Separation by density
(isopycnic centrifugation);Percoll – physical properties;Storage of Percoll;Sterilization of Percoll solutions;How to make and use gradients of Percoll—Making and diluting a stock solution of Percoll;How to make and use gradients of Percoll—Diluting stock solutions to lower densities;Tips of making and use gradients of Percoll ;1. Percoll was diluted 9:1 (vol/vol) with 1.5 M NaCl,
2. Put 10 ml of the Percoll solution into 15-ml Corex tubes and centrifuged at 19,240 gav for 15 min at 20°C. (swinging bucket rotor )
3. Approximately 2 × 109 cells (200 OD600) were pelleted, resuspended in 1 ml Tris buffer, overlaid onto the preformed gradient, and centrifuged at 400 gav for 60 min.;Percoll gradient purification of spores;Instrument and operation;Instrument and operation;Instrument and operation;Instrument and operation—data export;References and applications; contrast
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