Material for promoting cell growth adhering to wall and preparation method of material
A technology of adherence and cells, which is applied in the field of materials that promote cell adherence growth and its preparation, can solve the problems affecting cell proliferation and growth, and the difficulty of separating downstream products of cultured cells, etc., to achieve radiation sterilization and adherence good effect
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Embodiment 1
[0077] Take 0.68 μg / ml mussel mucin solution and add it to a 6-well culture plate, the amount added to each well is 1.43 mL, then the concentration of mussel mucin in each well is 0.1 μg / cm 2 . Dry the culture plate in an oven at 40°C for later use.
[0078] BEK-21 cells were cultured in MAP-coated plates and empty plates (control group without MAP coating), and the cell growth was observed at 2, 12 and 48 hours respectively. The medium was DMEM without adding serum. The result is as Figure 1a , 1b , 2a, 2b, 3a, 3b.
[0079] Compared with the control, the cells on the culture plate coated with mussel mucin had adhered and expanded after 2 hours, and the cells on the culture plate coated with mussel mucin had grown into a monolayer after 48 hours.
Embodiment 2
[0081] Take 0.5mg / ml mussel mucin solution and add it to a 6-well culture plate, the amount added to each well is 1.425mL, then the concentration of mussel mucin in each well is 75μg / cm 2 . Dry the plate in an oven at 55°C.
[0082] BHK-21 cells were cultured in MAP-coated plates and empty plates (control group without MAP coating), and the cell growth was observed at 2, 12 and 48 hours respectively. The medium was DMEM and 10% fetal bovine serum was added. . The result is as Figure 4a , 4b , 5a, 5b, 6a, 6b.
[0083] Compared with the control, the cells on the culture plate coated with mussel mucin had adhered and expanded after 2 hours, and the cells on the culture plate coated with mussel mucin had grown into a monolayer after 48 hours.
Embodiment 3
[0085] Take the mussel mucin solution and add it to a culture bottle with a bottom area of 25 square centimeters to make the mussel mucin density reach 0.1 μg / cm 2 . Dry the plate in an oven at 20°C.
[0086] The mesenchymal stem cells were cultured in MAP-coated plates and empty plates (control group without MAP coating), and the cell growth was observed at 2 and 12 hours, respectively. The medium was DMEM, supplemented with 10% fetal bovine serum. The result is as Figure 7a , 7b , 8a, 8b.
[0087] Compared with the control, in the culture plate coated with mussel mucin, the cells had adhered to the wall and extended after 2 hours, and the number of cells increased significantly after 12 hours.
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