Preparation of flounder erythrocyte outer membrane protein
A technology of flounder red blood cells and outer membrane proteins, which is applied in the collection and processing of fish red blood cells and the preparation of red blood cell outer membrane proteins, can solve the problems of less red blood cell immunity, lack of in-depth analysis and identification of red blood cell immune molecules, and unknown mechanism of action, etc.
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Embodiment 1
[0035] The specific operation steps are:
[0036] (1) Blood was collected from the tail veins of four experimental flounder with a body length of about 20 cm using a 5 mL disposable sterile syringe, and the peripheral blood of the flounder was mixed with Arbori anticoagulant at a ratio of 1:1. Collect the anticoagulated blood and store it in an ice box.
[0037] (2) Separation of erythrocytes in peripheral blood of flounder with specific gravity of 1.08-1.09 lymphocyte separation medium. The anticoagulated blood was diluted 1:1 with 0.1M PBS buffer, mixed with lymphocyte separation medium in a ratio of 1:2, and centrifuged horizontally at 3000rpm for 15min at 4°C. After centrifugation, the peripheral blood cells were divided into 4 layers, and the separation liquid, white blood cells and plasma in the upper layer were carefully sucked away, and the red blood cell pellet in the bottom layer was centrifuged and washed 3 times with 0.1M PBS buffer at 4°C, and the supernatant was...
Embodiment 2
[0045] The specific operation steps are:
[0046] (1) Blood was collected from the tail veins of four experimental flounders with a body length of about 20 cm using a 5 mL disposable sterile syringe, and mixed with the peripheral blood of the flounder at a ratio of 1:1.5 with Alfred anticoagulant. Collect the anticoagulated blood and store it in an ice box.
[0047] (2) Separation of erythrocytes in peripheral blood of flounder with specific gravity of 1.08-1.09 lymphocyte separation medium. The anticoagulated blood was diluted 1:1 with 0.1M PBS buffer, mixed with lymphocyte separation medium in a ratio of 1:2, and centrifuged horizontally at 3000rpm for 15min at 4°C. After centrifugation, the peripheral blood cells were divided into 4 layers, and the separation liquid, white blood cells and plasma in the upper layer were carefully sucked away, and the red blood cell pellet in the bottom layer was centrifuged and washed 3 times with 0.1M PBS buffer at 4°C, and the supernatant...
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