Establishment method and application of fish targeted gene nutrition regulation and control cell model
A technology of targeting genes and nutritional regulation, applied in artificial cell constructs, animal cells, vertebrate cells, etc., can solve the problem of inability to continuously pass on, and achieve the effect of good growth state, maintaining vitality, and stable cell proliferation.
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Embodiment 1
[0035]Construction Method for Construction of Targeting Gene Nutritional Regulation Model:
[0036](1) Grassfish Choice: Grass Fish Choose a 1st-year-old healthy grassfish of 25g / tail;
[0037](2) Formation base, primary, passaged cell culture medium and cell cleaning liquid:
[0038]Senior medium: DMEM contains 10 vol% of fetal bovine serum, 1 vol% pyruvate, 1 vol% non-essential amino acid, 1 vol% L-glutamine, 0.1 vol% β-mercaptoethanol and 1 vol% double Anti-(penicillin 100,000 IU / L and streptomycin 100 mg / L).
[0039]Cell cleaning liquid: D-PBS contained 2% bis-resistant (penicillin 200,000 qu / L and streptomycin 200 mg / L).
[0040]Chuanca cell culture fluid: DMEM contains 10 vol% of fetal bovine serum, 1 vol% pyruvate, 1 vol% non-essential amino acid, 1 vol% L-glutamine, 0.1 vol% β-mercaptoethanol and 1 vol% double The concentration of epidermal cell growth factor concentration in anti-(penicillin 100,000 qu / l and streptomycin 100 mg / L) cell culture medium is 5-10 ug / ml.
[0041](3...
Embodiment 2
[0051]Verify the effect of diptide and polypeptide on the proliferation of grass fish intestinal epithelial cells and the expression of polypeptide on PEPT1.
[0052]Embodiment 1 Chinese grass fish intestinal epithelial cell (5th generation) count adjusts cell concentration to 1 × 105 / ml inoculated in 96 holes, 100 μL per well, 3 complements of each group of cells, overnight culture plates, add GHRELIN, ALA-GLN, GHRELIN + ALA-GLN, for the second day, and the control only base. After 24 hours of cell culture, 10 μl of 5 mg / ml MTT solution (note that air bubbles) were added (noted), and the culture was terminated after 4 to 6 hours, and 150 ul DMSO was added, and the low speed was oscillated at low speed on the bed to sufficiently dissolve the crystalline product. Each hole absorbance value at 490 nm was detected at an enzyme-linked immunoassay. At the same time, the zero hole (medium, MTT, DMSO) is set. Record results, the result is likeimage 3 .
[0053]Example 1 Inoculated into 6-well...
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