Special culture medium for lung cancer organoid and culture method
A culture method and organoid technology, which is applied in the special medium and culture field of lung cancer organoids, and can solve the problems of difficulty in the development of lung cancer organoids, etc.
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Embodiment 1
[0038] This example provides a special culture medium and culture method for lung cancer organoids, including basal medium and specific additive factors; the specific additive factors include the following final concentrations of components: GSK429286A, 5uM; Y27632, 12.5uM; EGF BMP4, 150ng / ml; Human FGF4, 300ng / ml; Insulin-Transferrin-Selenium, 1.5x; B27, 0.75x; all-trans retinoic acid, 0.5uM; KGF, 200ng / ml; DAPT, 5mM ; GlutaMAX, 1.25x; R-Spondin-1, 300ng / ml; CHIR99021, 5uM; 8-Br-cAMP, 150nM; BSA, 0.5%; 3-isobutyl-1-methylxanthine, 50nM; Percentages are mass percentages.
[0039] Lung cancer organoid culture methods include:
[0040](1) Wash the lung cancer tissue taken out with normal saline, cut it into pieces on ice, add 10ml of digestion solution 1 to resuspend, wherein digestion solution 1 includes 500ng / ml of Hydrocortistone and 500U / ml of Collagenase enzyme type IV, transfer to 37 °C, 100rpm shaker for 2 hours, after the digestion is complete, add 5ml of HBSS to stop ...
Embodiment 2
[0045] This example provides a special medium and culture method for lung cancer organoids, including basal medium and specific additive factors; the specific additive factors include the following final concentration components: GSK429286A, 15uM; Y27632, 6uM; EGF, 200ng / ml; BMP4, 50ng / ml; Human FGF4, 550ng / ml; Insulin-Transferrin-Selenium, 0.8x; B27, 1.5x; all-trans retinoic acid, 0.6uM; KGF, 100ng / ml; DAPT, 15mM; GlutaMAX, 0.75x; R-Spondin-1, 600ng / ml; CHIR99021, 8uM; 8-Br-cAMP, 80nM; BSA, 0.3%; 3-isobutyl-1-methylxanthine, 150nM; is the mass percentage. The lung cancer organoid culture method is the same as that in Example 1. Figure 5 The topography of lung cancer organoids obtained after 14 days of culture is provided, and the formed tumor organoid cells are spherical in shape and large in diameter.
Embodiment 3
[0047] This example provides a special culture medium and culture method for lung cancer organoids, including basal medium and specific additive factors; the specific additive factors include the following final concentrations of components: GSK429286A, 2.5uM; Y27632, 20uM; EGF BMP4, 30ng / ml; Human FGF4, 300ng / ml; Insulin-Transferrin-Selenium, 2x; B27, 0.5x; all-trans retinoic acid, 1uM; KGF, 10ng / ml; DAPT, 20mM; GlutaMAX , 0.5x; R-Spondin-1, 1000ng / ml; CHIR99021, 1uM; 8-Br-cAMP, 150nM; BSA, 0.1%; 3-isobutyl-1-methylxanthine, 150nM; mass percentage. The lung cancer organoid culture method is the same as that in Example 1. Figure 6 The topography of lung cancer organoids obtained after 14 days of culture is provided. The formed tumor organoid cell spheres are regular in shape, tightly connected between cell spheres, and the size is uniform and controllable.
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