A method for constructing a flounder testis cell line
A construction method and cell line technology, applied in the field of seawater fish cell culture, can solve problems such as the establishment of cell lines with no gonad tissue
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Embodiment 1
[0024] The establishment method of flounder testis cell line, the steps are as follows:
[0025] 1) Preparation of cell culture medium: take Hyclone company DF12 culture medium, add fetal bovine serum accounting for 20% of the total volume of cell culture medium to the culture medium, 10ng / ml recombinant human basic fibroblast growth factor (Recombinant HumanFGFb, bFGF) , 15ng / ml recombinant human epidermal growth factor (Recombinant Human EGF, EGF), 100U / mL penicillin, 100μg / mL streptomycin, pH value is 7.2, stored at 4°C for later use.
[0026] 2) Primary culture: under aseptic conditions, the testis tissue of healthy flounder with a body weight of 347.5 g was taken, and placed in a sterile glass plate with 4 mL of Hyclone DF12 culture solution supplemented with 400 U / mL penicillin and 400 μg / mL streptomycin After soaking for 5 minutes, discard the culture medium, rinse the testis tissue twice with 2mL PBS (pH 7.2), suck out the PBS, cut the testis tissue into minced pieces,...
Embodiment 2
[0029] Identification and application of testis cell line of flounder
[0030] 1) Cryopreservation and recovery of cells
[0031] Freezing of cells:
[0032] Select the above-mentioned subcultured testicular cells in the exponential growth phase with a cell density of more than 90% in different generations, and digest them according to the conventional method. After digestion, the cells shrink under the microscope and discard the trypsin solution. Completely, add 2 mL of fresh cell culture medium prepared in step 1) of the above-mentioned embodiment to the original bottle to prepare cell suspension. Transfer the cell suspension to a 15mL centrifuge tube, centrifuge at 2200g for 3min, discard the supernatant. Suspend the cells with 2 mL of pre-cooled cryopreservation solution (Hyclone DF12 cell culture medium containing 10% dimethyl sulfoxide), and transfer to 2 mL cryopreservation tubes, put the cryopreservation tubes into the programmed cooling box for 4 ℃ for 30 minutes, ...
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