Separation method for separating peripheral blood immune cells
A technology of immune cells and separation methods, applied in cell dissociation methods, blood/immune system cells, animal cells, etc., can solve the problems affecting the quality of the separation effect, the separation of the lymphocyte layer, and the influence of the separation effect, etc., to achieve Small raw material uncertainty, low operating experience, enhanced immunity and regenerative effects
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Embodiment 1
[0026] A method for isolating immune cells from peripheral blood, comprising the steps of:
[0027] Step 1: Dilute the anticoagulant-treated peripheral blood with normal saline or serum-free medium to obtain a cell suspension;
[0028] Step 2: Add the separation liquid containing dextran, phospholipid, trehalose and amino acid into the centrifuge tube, the volume of the separation liquid is not more than 1 / 2 of the volume of the centrifuge tube;
[0029] Step 3: Spread the cell suspension on the separation medium, centrifuge at 8-25°C, 200g-800g, 10-30min, and absorb the buffy coat cells.
[0030] Among them, the preparation method of the separation liquid is: in an environment with local 100-level laminar flow purification conditions, at 20 ° C, 4 g of dextran, 3 g of phospholipids, 5 g of trehalose, and ultra-low viscosity alginic acid Sodium 0.5g, Meglumine Diatrizoate 5g, Polydiallyldimethylammonium Chloride 0.1g, L-Valine 0.01g and L-Leucine 0.009g are fully dissolved in...
Embodiment 2
[0032] A method for isolating immune cells from peripheral blood, comprising the steps of:
[0033] Step 1: Dilute the anticoagulant-treated peripheral blood with normal saline or serum-free medium to obtain a cell suspension;
[0034] Step 2: Add the separation liquid containing dextran, phospholipid, trehalose and amino acid into the centrifuge tube, the volume of the separation liquid is not more than 1 / 2 of the volume of the centrifuge tube;
[0035] Step 3: Spread the cell suspension on the separation medium, centrifuge at 8-25°C, 200g-800g, 10-30min, and absorb the buffy coat cells.
[0036]Among them, the preparation method of the separation liquid is: in an environment with local 100-level laminar flow purification conditions, at 20 ° C, 2.5 g of dextran, 0.3 g of phospholipid, 7 g of trehalose, ultra-low viscosity Sodium alginate 1g, diatrizoate meglumine 3g, polydiallyl dimethyl ammonium chloride 0.04g, L-valine 0.009g and L-leucine 0.012g are fully dissolved in ste...
Embodiment 3
[0038] A method for isolating immune cells from peripheral blood, comprising the steps of:
[0039] Step 1: Dilute the anticoagulant-treated peripheral blood with normal saline or serum-free medium to obtain a cell suspension;
[0040] Step 2: Add the separation liquid containing dextran, phospholipid, trehalose and amino acid into the centrifuge tube, the volume of the separation liquid is not more than 1 / 2 of the volume of the centrifuge tube;
[0041] Step 3: Spread the cell suspension on the separation medium, centrifuge at 8-25°C, 200g-800g, 10-30min, and absorb the buffy coat cells.
[0042] Among them, the preparation method of the separation liquid is: in an environment with local 100-level laminar flow purification conditions, at 20 ° C, 2 g of dextran, 2 g of phospholipids, 5.5 g of trehalose, and ultra-low viscosity seaweed Sodium phosphate 0.6g, diatrizoate meglumine 4.5g, polydiallyl dimethyl ammonium chloride 0.09g, L-valine 0.01g and L-leucine 0.011g are fully ...
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