Method for separating babylonia areolata granular cells and clear cells by Percoll serving as medium
A technology of snail snails and granule cells, applied in cell dissociation methods, biochemical equipment and methods, animal cells, etc., can solve the problems of poor understanding of the immune function of shellfish blood cells, etc., to reduce the probability of pollution, good application Foreground, simple effect
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[0024] 1. Preparation of Density-Optimized Percoll Solution
[0025] The density of the Percoll stock solution is 1.13g / mL; use the anticoagulant ZA solution to prepare Percoll solutions with a volume fraction of 38% and a volume fraction of 35%.
[0026] 2. Blood cell concentration adjustment
[0027] Suspend the hemocytes of the snail and use the anticoagulant ZA solution to adjust the blood cell density of the snail to (2–5)×10 5 Cells / mL to obtain the blood cell suspension of the snails.
[0028] 3. Ratio of separating liquid and sample volume
[0029]Using a 15mL centrifuge tube, add 3mL of Percoll solution with a volume fraction of 38% and 2mL of blood cell suspension of P.
[0030] 4. Two-step centrifugation
[0031] Centrifuge at 1300g at 4°C for 45min. The solution is divided into three layers: the upper layer, the lower layer and the interface layer. Separately pack the upper layer solution, the lower layer solution, and the interface solution between the upper a...
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