Serum-free induced pluripotent stem cell cryopreservation liquid and cryopreservation method
A technology for pluripotent stem cells and cryopreservation, applied in the field of induced pluripotent stem cell cryopreservation, can solve the problems of residual pluripotent stem cells, protein denaturation, cell damage, etc., to maintain cell viability, prevent cell differentiation, and reduce cell proliferation. damage effect
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Embodiment 1
[0031] Example 1. Preparation of Induced Pluripotent Stem Cell Cryopreservation Solution
[0032] The freezing solution consists of liquid A and liquid B. The volume ratio of liquid A to liquid B is 1:1.
[0033] Each 100mL Freezing Solution A contains the following components:
[0034]
[0035] Each 100mL freezing solution B contains the following components:
[0036]
[0037]
[0038] Preparation method: Mix all ingredients to obtain liquid A and liquid B respectively, and store at 4°C.
Embodiment 2
[0039] Example 2. Application of cryopreservation solution in cryopreservation of induced pluripotent stem cells
[0040] Freezing method:
[0041] After digesting the induced pluripotent stem cells in the logarithmic growth phase, centrifuge at 800rpm / min for 5 minutes to remove the supernatant, resuspend with an appropriate amount of liquid A of the present invention, and perform cell counting, then add an equal amount of liquid B to make the cells The concentration is 1×10 6 -6×10 6 cells / mL, and then 1 mL / tube was dispensed into 1.8 mL cell cryopreservation tubes, placed in a programmed cooling box at -80°C for programmed cooling, and transferred to liquid nitrogen for storage after 24 hours.
[0042] Inspection of frozen storage results:
[0043] 1. Morphological observation of pluripotent stem cells after resuscitation
[0044] The frozen cells were resuscitated, and the medium was changed every day, and the morphology was observed under a microscope, and pictures we...
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