Culture medium for culturing recurrent bladder cancer biopsy sample organoid and culture method thereof
A culture medium, bladder cancer technology, applied in the direction of cell culture active agent, culture process, tissue culture, etc., can solve the problems of low success rate of culture, obstacles to precise treatment of bladder cancer, etc., and achieve the effect of stable and reliable source and low cost
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Embodiment 1
[0055] Embodiment 1, improved culture medium 1
[0056] DMEM / F12K medium (1:1), ascorbic acid (10mg / L), L-glutamic acid (50mg / L), sodium selenite (0.05mg / L), ethanolamine hydrochloride (20mg / L), Ammonium metavanadate (5×10 -4 mg / L), manganese chloride tetrahydrate (7×10 -5 mg / L), R-spondin 1 (200ng / ml), Noggin (20ng / ml), N2:B27 (1:1), glutamine supplement (1×), HEPES (1×), nicotinamide ( 20mM), Normocin TM (1×), N-acetylcysteine (2 mM), A83-01 (10 μM), EGF (100 ng / ml), FGF10 (20 ng / ml), heparin (100 IU / ml).
Embodiment 2
[0057] Embodiment 2, improved culture medium 2.
[0058] DMEM / F12K medium (2:1), ascorbic acid (2mg / L), L-glutamic acid (100mg / L), sodium selenite (0.1mg / L), ethanolamine hydrochloride (50mg / L), Ammonium metavanadate (20×10 -4 mg / L), manganese chloride tetrahydrate (15×10 -5 mg / L); R-spondin 1 (500ng / ml), Noggin (50ng / ml), N2:B27 (1:2), glutamine supplement (1×), HEPES (1×), nicotinamide ( 5mM), Normocin TM (1×), N-acetylcysteine (2 mM), HGF (100 ng / ml), DMSO (1%, v / v), CHIR99021 (50 μM).
Embodiment 3
[0059] Example 3. Comparison of recurrent bladder cancer organoids cultured in two improved media and primary bladder cancer (PNAS)
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