Culture medium for epithelial cells of esophageal squamous carcinoma, culture method and application thereof
A technology for esophageal squamous cell carcinoma and epithelial cells, applied in the field of medicine, can solve the problems of necrosis, complicated and time-consuming operation, high cost, etc., and achieves the effects of high efficiency, controllable culture cost, and improved success rate.
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[0084] [Preparation Example of MST1 / 2 Kinase Inhibitor]
[0085] In the present specification, an MST1 / 2 kinase inhibitor refers to any inhibitor that directly or indirectly negatively regulates MST1 / 2 signal transduction. In general, MST1 / 2 kinase inhibitors, for example, bind to MST1 / 2 kinase and reduce its activity. Due to the similarity in the structures of MST1 and MST2, MST1 / 2 kinase inhibitors may also be, for example, compounds that bind to MST1 or MST2 and reduce their activity.
[0086] 1. Preparation of MST1 / 2 Kinase Inhibitor Compound 1
[0087] 4-((7-(2,6-difluorophenyl)-5,8-dimethyl-6-oxo-5,6,7,8-tetrahydropteridin-2-yl)amino)benzene Sulfonamide 1
[0088]
[0089] Methyl 2-amino-2-(2,6-difluorophenyl)acetate (A2): In a round bottom flask was added 2-amino-2-(2,6-difluorophenyl)acetic acid (2.0 g) Methanol (30 mL) was then added, followed by the dropwise addition of thionyl chloride (1.2 mL) under ice-cooling. The reaction system was reacted overnight ...
Embodiment 1
[0102] Isolation of Primary Human Esophageal Squamous Cell Carcinoma Epithelial Cells
[0103] The tissue samples of esophageal squamous cell carcinoma were obtained from three cases of patients with esophageal squamous cell carcinoma who had been explained and obtained consent, and they were respectively sample numbers 0F0060, 0F0061, and 0F0062. The following is an example of a sample (No. 0F0060) for illustration.
[0104] The above tissue samples were collected within half an hour of the patient's surgical resection or biopsy. More specifically, under sterile conditions, tissue samples from non-necrotic sites were removed in a volume of 0.5 cm 3 Above, it was placed in pre-cooled 4mL tissue transport solution (see Table 1 for specific preparation), and the transport solution was contained in a 5mL plastic sterile cryopreservation tube with a cover (purchased from Guangzhou Jiete Biology), and the cold chain (0- 10°C) to the laboratory.
[0105] Table 1 Formula of tissue...
Embodiment 2
[0116] Optimization of culture medium for primary esophageal squamous cell carcinoma epithelial cells
[0117] (1) The role of different factors
[0118] extracellular matrix gel (manufactured by BD Biotechnology Co., Ltd.) Use serum-free DMEM / F12 medium at a dilution ratio of 1:100 to prepare an extracellular matrix dilution, add 500 μl / well of the extracellular matrix dilution to a 48-well culture plate to completely cover it Bottom of culture plate wells. Place in a 37°C incubator for 1 hour. After 1 hour, the extracellular matrix dilution was removed to obtain a Matrigel-coated culture plate.
[0119] Preparation of basal medium (abbreviated as BM): add 0.2 volume % Primocin (purchased from Invivogen, the concentration is 50 mg / mL) to the commercially available DMEM / F-12 medium to obtain a final concentration of 100 μg / mL, and prepare Get BM.
[0120] Next, different types and different concentrations of additive factors (Table 3) were added to the basal medium (BM) ...
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