Silver crucian carp back fin cell line
A cell line and dorsal fin technology, applied in the field of life science, to achieve the effect of good material resources, good effect and manpower saving
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Embodiment 1
[0031] The construction method of embodiment 1 gibel carp dorsal fin cell line
[0032] 1. Preparation of cell culture medium
[0033] Take the M199 medium of GIBCO company, add fetal bovine serum accounting for 10-20% of the total volume of the medium (the percentages mentioned below are all volume percentages unless otherwise specified), and the final concentration is 20ng / ml basic fibroblast growth factor (bFGF), epidermal growth factor (EGF) with a final concentration of 1 ng / ml, stored at 4°C, and used for later use.
[0034] 2. Primary culture
[0035] Cut off the dorsal fin of gibel carp, then disinfect it with 75% alcohol, and then use 1000IU mL -1 Penicillin, 1000ug mL -1 Streptomycin was used to remove the mucus on the dorsal fin of gibel carp, followed by 2.5ug mL -1 Wash 3 times with amphotericin B in D-PBS. After rinsing, cut the dorsal fin to about 1 mm with scissors under sterile conditions 3 The small pieces were then soaked in 0.25% trypsin and 0.02% EDT...
Embodiment 2
[0039] Embodiment 2 Gibel carp dorsal fin cell line
[0040] After in vitro culture, the present invention has obtained a strain of gibel crucian carp dorsal fin cell line (SCC-DF cell line, Silver crucian carp dorsal fin cell line) with stable passage and uniform components, which has been passed down to date.
[0041] The silver crucian carp dorsal fin cell line that the present invention obtains has been preserved in the China Typical Culture Collection Center, the silver crucian carp dorsal fin cell line SCC-DF, its preservation number is CCTCC NO:C201525, and the classification is called silver crucian carp (Carassius C.auratus), The address of the Chinese Type Culture Collection Center is Wuhan University, Wuhan City, Hubei Province, China, and the date of deposit is March 27, 2015.
[0042] Further, the gibel carp dorsal fin cell line has the following biological characteristics:
[0043] 1) The cells isolated from the primary cell near the tissue block exhibit the mor...
Embodiment 3
[0047] Embodiment 3 virus infection experiment
[0048] 1. Experimental method
[0049] 1. Virus infection
[0050] The cultured golden carp pelvic fin cell line was transferred to a 6-well plate and grown adherently overnight. Contain crucian carp herpesvirus II, CyHV-2) and alkaline phosphate buffer, PBS (negative control group) to take 500 μl of infected cells, incubate for 1 hour, discard the supernatant, wash 3 times with PBS, add 500 μl of complete medium Place them in an incubator and observe the growth of the cells every day.
[0051] 2. Drawing of virus replication curve in cell supernatant
[0052] Transfer the cells to a 24-well plate, infect the virus according to step 1, take the supernatant every 24 hours, and discard the precipitate by high-speed centrifugation, and extract DNA from the supernatant for fluorescent quantitative PCR detection according to the following steps.
[0053] 3. Extraction of viral DNA
[0054] (1) Add an equal volume of PBS buffer, ...
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