Cryptocaryon irritans recombinant protein vaccine as well as preparation method and application
A technology for stimulating Cryptonucleus and proteins, applied in the directions of botanical equipment and methods, biochemical equipment and methods, applications, etc., can solve the problem of the difficulty in preventing the infection of marine fish by stimulating Cryptonucleus and inhibiting the DNA sequence of antigens. and other problems, to achieve the effect of excellent expression effect, large amount of protein expression, and maximum amount of protein expression
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Embodiment 1
[0046] 1. Collection and cultivation of parasites
[0047] Fish infected with Cryptocaryon stimuli were collected from fish rafts in Ningde and Putian and raised in an aquarium with a water temperature of 25°C. After the cystic body (tomont) was collected from the bottom of the aquarium, it produced ciliated larvae and infected pomfret (Trachinotus ovatus) or pearl gentian (E. fuscoguttatus X gentian E. Lanceolatus).
[0048] The process of parasite culture used in this application is as follows: use a brush or a small paint brush to gently sweep and collect cysts that stimulate Cryptocaryon from the bottom of the aquarium, and use seawater to wash off excess residue or mucous membranes , the cyst body is cultured on a petri dish with filtered sea water, and cultured at room temperature for 3-7 days. The ciliated larva (theront) that stimulates Cryptocaryonia will be produced from the cyst body. At this time, the solution containing the ciliated larvae can be collected by ce...
Embodiment 2
[0087]The difference between this example and Example 1 is that the constructed recombinant plasmid pFNCJ was transformed into the competent cells of BL21DE3, and then evenly spread on the LB plate containing 48ug / mL kanamycin sulfate, and then placed upside down at 38 ℃ incubator overnight, select single clones from the transformed plates, inoculate into LB medium containing 48ug / mL of kanamycin sulfate, cultivate at 38 ℃ shaker at 580rpm / mim, until the OD600 is 0.5-0.8, IPTG was added to the culture medium in the test tube to a final concentration of 0.5 mM, and then placed at 28°C to induce expression.
[0088] The C. stimuli recombinant protein vaccine is mixed into the feed or bait of the vaccine-use object, so as to prevent the vaccine-use object from being infected with C. stimuli.
Embodiment 3
[0090] The difference between this example and Example 1 is that the constructed recombinant plasmid pFNCJ was transformed into BL21DE3 competent cells, and then evenly spread on the LB plate containing 52ug / mL kanamycin sulfate, and then placed upside down at 36 ℃ incubator overnight, select single clones from the transformed plates, inoculate into LB medium containing 52ug / mL kanamycin sulfate, cultivate at 36 ℃ shaker at 620rpm / mim, until the OD600 is 0.5-0.8, IPTG was added to the culture medium in the test tube to a final concentration of 0.5 mM, and then placed at 37°C to induce expression.
[0091] The C. stimuli recombinant protein vaccine is mixed into water to soak the object of use of the vaccine, so as to prevent the object of use of the vaccine from being infected with C. stimuli.
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