Umbilical cord blood component synchronous separation kit and use method thereof
A synchronous separation and kit technology, applied in the field of umbilical cord blood separation, can solve the problems of underutilization, lack of separation, waste of umbilical cord blood resources, etc., and achieve the effect of promoting full utilization
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Embodiment 1
[0035] Embodiment 1: a kind of synchronous separation kit of each component of umbilical cord blood
[0036] Including No. A dilution solution, No. B1 separation solution, No. B2 separation solution, No. C washing solution, and No. D lysate; also includes consumables, including 10 50ml centrifuge tubes, 20 15ml centrifuge tubes, and 10 10ml pipettes , 5 3ml Pasteur pipettes, 175cm 2 3 cell culture flasks;
[0037] The No. A dilution is 0.9% physiological saline, in which human serum albumin is added, and the mass concentration of human albumin added to the No. A dilution is 0.75%;
[0038] The No. B1 separating liquid is prepared by the following method: 40% polysucrose liquid is prepared into a polysucrose liquid with a mass concentration of 9% with Hank's solution; then 60% compound diatrizoate meglumine The injection was formulated with Hank's solution to form a compound diatrizoate solution with a mass concentration of 34%; finally, 9% polysucrose solution and 34% compou...
Embodiment 2
[0042] Embodiment 2: a kind of synchronous separation kit of each component of umbilical cord blood
[0043] Basically the same as Example 1, the difference is that the No. A dilution is 0.9% physiological saline; the No. C washing solution is about pH 7.4 without Ca 2+ and Mg 2+ of PBS solution.
Embodiment 3
[0044] Embodiment 3: A method for synchronously separating components in cord blood with the cord blood components synchronous separation kit described in Example 1
[0045] ① Divide 100ml of voluntary donated cord blood into two 50ml centrifuge tubes a, centrifuge at 2500rpm for 10 minutes, then absorb the upper plasma layer into centrifuge tube b;
[0046] ② Add an equal volume of No. A solution to the separated centrifuge tube a and mix well, then carefully add 3ml No. B1 separation solution, 3ml B2 No. separation solution and the mixed solution in centrifuge tube a to the 15ml centrifuge tube along the wall. In the method, centrifuge at 2000rpm for 25 minutes and separate into five layers: use a Pasteur pipette to draw the first layer into the centrifuge tube c, and draw the second layer (circular milky white cell layer) mononuclear cell layer into the centrifuge tube d. Aspirate the neutrophil layer of the third layer (annular milky white cell layer) into the centrifuge t...
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