Grass goldfish pelvic fin cell line constructing method
A construction method, the technology of goldfish grass, applied in the field of cell biology, can solve the problems that the pelvic fin cell line of goldfish grass has not been reported, and achieve the effect of strong cell reproduction ability
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Embodiment 1
[0030] (1) Treatment of tissue blocks: cut off the pelvic fins of goldfish, put them in a penicillin-streptomycin double-antibody solution (distilled water configuration) with a concentration of 1000IU / ml, and place them for 30 minutes, then sterilize them in 75% alcohol for 2 minutes, and carry out the first Disinfection; then wash 3 times with D-PBS containing 2.5ug / ml amphotericin B for secondary disinfection; after rinsing, cut the pelvic fins to about 1mm with scissors under sterile conditions 3 The small pieces of tissue were soaked in 0.25% trypsin and 0.02% EDTA for 10 minutes, and then digested with 0.5% hyaluronidase for 1 hour;
[0031] (2) Primary culture: collect the digested tissue fragments and transplant them to the bottom of 25cm 2In the cell culture flask, keep the bottom temperature at 25 °C. After 15 hours, add 2ml grass gold carp pelvic fin cell special-purpose proliferating culture fluid (culture fluid formula is to contain 18v / v% fetal calf serum, 15ng / ...
Embodiment 2
[0071] Example 2 The cell line is applied to the detection of crucian carp herpesvirus II (CyHV-2)
[0072] 1. Experimental method
[0073] 1. Virus infection
[0074] The cultured golden carp pelvic fin cell line was transferred to a 6-well plate and grown adherently overnight. Take 500 μl of infected cells from the positive sample (containing crucian carp herpesvirus II, CyHV-2) and the negative sample (alkaline phosphate buffered saline, PBS) to be detected respectively, incubate for 1 hour, discard the supernatant, wash 3 times with PBS, Add 500 μl of complete medium and place it in an incubator for culture, and observe the cell growth every day.
[0075] 2. Extraction of viral DNA
[0076] (1) Add an equal volume of PBS buffer, mix well, centrifuge at 8000rpm for 5 minutes, and discard the supernatant;
[0077] (2) Add 20 μL of proteinase k. Incubate in a water bath at 56°C for 3 hours;
[0078] (3) Centrifuge at 8000rpm for 5 minutes, take 750μL of supernatant and p...
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