Method for preparing chook Marek's disease virus infection detection antigen
A Marek's disease, Marek's technology, applied in the direction of measuring devices, instruments, scientific instruments, etc., to achieve high work efficiency, easy operation, and reduce production costs
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Embodiment 1
[0026] Embodiment one: (truncated first, then divided and concentrated)
[0027] a. Remove the tested and customized screening membrane modules that allow the MDV A antigen to pass through effectively, such as hollow fiber ultrafiltration membrane modules marked with a molecular weight cut-off of 75,000, and roll-type ultrafiltration membrane modules with a molecular weight cut-off of 150,000. Seal the blocking plate, and install it in an appropriate ultrafiltration device after draining the maintenance fluid filled into it;
[0028]b. Open the liquid inlet valve, concentrated liquid return regulating valve, and liquid permeable valve to the maximum flux position, turn on the booster pump, rinse with clean water at room temperature (20-30°C) for 20-30 minutes, and adjust through the concentrated liquid return flow The operating pressure of the valve control is within the working range (0.02~0.1Mpa);
[0029] C, will contain the raw material liquid of MDV A antigen, as the sup...
Embodiment 2
[0032] Embodiment two: (remove small and concentrate earlier, then remove large purification, concentrate again)
[0033] With reference to the procedures, parameters and process conditions of Example 1, first use the custom-made maximum molecular weight cut-off membrane module capable of effectively retaining the MDV A antigen to carry out ultrafiltration concentration and removal of small molecular impurities on the thin raw material solution containing the MDV A antigen. When it is concentrated to a specified multiple or the permeate is reduced to a very low flow rate, the permeate is discarded and the retentate is collected. The residue in the equipment is also incorporated into the retentate after being circulated and washed with purified water (or physiological saline, or PBS buffer solution). Then, add not less than 3 times the volume of clean water or physiological salt or PBS buffer to the liquid for mixing, and use the ultrafiltration with the minimum molecular weigh...
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