Preparation method of fluorescence antibody for detecting Newcastle disease virus and solid-phase immunofluorescence detection assay kit
A technology for Newcastle disease virus and anti-Newcastle disease virus, applied in the field of immunofluorescence detection, can solve the problems of high production cost of markers, reduced fluorescence detection sensitivity, affecting fluorescence detection sensitivity, etc. Small, the effect of improving sensitivity
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[0026] RPE preparation: Add 6 times the volume of 20mM acetate buffer (pH5.8) to cryopreserved Polytubuleum, swell at 4°C for 24 hours, filter and extrude with multi-layer gauze to obtain a brown extract, add solid ammonium sulfate to the extract To a concentration of 60% (w / v), place at 4°C for 24 hours, collect the precipitate by centrifugation, dissolve the precipitate in 20mM acetate buffer (pH5.8), and then wash with 20mM acetate buffer (pH5.8) at 4°C After dialysis overnight, the dialysate was added to a DEAE Sepharose Fast Flow anion exchange column pre-equilibrated with 20mM acetate buffer (pH5.8) (containing 50mM NaCl), and the excess on the anion exchange column was washed with 20mM acetate buffer (pH5.8). The sample and impurity, with 20mM acetic acid buffer (pH4.0) (containing 50mM NaCl) one step elution can get a lot of pure RPE, the purity of the purified Polytubella RPE reaches electrophoretic purity, and the purity index is A 620 / A 280 >5.2, the structural fo...
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