Oplegnathus punctatus brain cell line as well as construction method and application thereof
A technology of porphyra and brain cells, which is applied in the field of using the brain tissue of porphyra to construct the brain cell line of porphyra, can solve the problems of economic loss in factory breeding of porpoise, and achieve reliable chromosome identification methods and high nutritional content. Full-scale, right-weight results
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Embodiment 1
[0025] Embodiment 1, the construction method of zebra sea bream brain cell line
[0026] The method for constructing the brain cell line of Pleurotus chinensis comprises three steps: 1. preparation of cell culture medium, 2. primary culture, 3. subculture
[0027] 1. Preparation of cell culture medium
[0028] The L-15 complete medium used in the zebra sea bream brain cell line is a mixture of 20% FBS, 10ng / mL bFGF, 50mmol / L 2-ME and 200IU / mL penicillin and streptomycin added to the L-15 culture medium. Store at 4°C.
[0029] Composition and final concentration of L-15 culture solution: 900mg / LD-galactose, 300mg / LL-glutamine, 550mg / L sodium pyrogluconate, pH value 7.0-7.4.
[0030] 2. Primary culture
[0031] Take a 300g freshly dead porpoise and put it in a clean plastic basin filled with 70% alcohol for 2 to 3 minutes, dissect the experimental fish and take out the brain tissue, put it in a petri dish and move it into an ultra-clean workbench for operation. Wash 3 times ...
Embodiment 2
[0035] The identification and application method of the Pleurotus bream brain cell line constructed in Example 1, including: 1. Freezing and recovery of cells, 2. Drawing of cell growth curves, 3. Chromosome analysis, 4. Transfection of GFP reporter gene . Specific steps are as follows:
[0036] 1. Cell cryopreservation and recovery
[0037] (1) Cell cryopreservation: Cells are properly frozen during the growth and passage of cells for future use in experiments. The cells of the Porphyra bream brain cell line 2-3 days after subculture were taken, the original medium in the culture flask was sucked off, the adherent cells were washed twice with PBS, and then the cells were digested and suspended with trypsin-EDTA digestion solution, and the collected Centrifuge at 1 200r / min for 5min in a centrifuge tube, resuspend in 0.75mL L-15 complete medium, and add an equal volume of freezing solution (L-15 medium containing 20% DMSO and 40% FBS by volume) to fully After mixing, tran...
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