Method for separating red corpuscle from whole blood
A technology of red blood cells and anti-red blood cell antibodies, which is applied in the field of separation of red blood cells, can solve the problems of complex operation and long time consumption, and achieve the effect of meeting different applications and needs, accelerating the speed of magnetic separation, and facilitating popularization and application
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Embodiment 1
[0025] Example 1: Method for Separating Red Blood Cells Using Phytohemagglutinin Coated Magnetic Particles
[0026] Take 100g of red beans, wash them with pure water, soak them in 200ml of pure water for 24 hours, use a juicer to crush the red beans into soybean milk, add 50ml of pure water during the crushing process to improve the grinding efficiency, and centrifuge the milk at 6000g for 30 Minutes, the supernatant was retained and further purified by saturated ammonium sulfate method to obtain pure plant lectin for future use.
[0027] According to the ratio of 20ug phytolectin coated with magnetic polymer microspheres (average diameter 100nm) solution of 10% concentration per milliliter, the magnetic polystyrene microspheres were dissolved in PBS (50mM, pH7.4) buffer solution in advance (concentration 10%, m / v), adding the lectin under the condition of rapid stirring, stirring (100 rpm) at room temperature for 30 minutes. Then add BSA to a final concentration of 0.2%, sti...
Embodiment 2
[0030] Example 2: Method for Separating Red Blood Cells Using Anti-erythrocyte Antibody Coated Magnetic Particles
[0031] Take 1 mg of anti-erythrocyte antibody purchased from Beijing Xinchuang Bioengineering Co., Ltd. According to the ratio of 20ug anti-erythrocyte antibody coated with 10% concentration of magnetic polyethylene microspheres (average diameter 100nm) solution per milliliter, the magnetic polyethylene microspheres were dissolved in PBS buffer (50mM pH7.4) in advance (concentration 10%) , m / v), under the situation of rapid stirring, add anti-erythrocyte antibody, stir (100 rev / min) reaction at room temperature for 30 minutes, add BSA to final concentration 0.2%, stir (100 rev / min) reaction at room temperature for 15 minutes , finally centrifuged at 10000g for 20 minutes, discarded the supernatant, resuspended the pellet with PBS (50mM pH7.4) buffer solution, and obtained the magnetic polyethylene microsphere solution labeled with anti-erythrocyte antibody (the f...
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