Method for preparing egg yolk antibody, egg yolk antibody prepared by method and application of egg yolk antibody
A yolk antibody, volume technology, applied in the direction of antibodies, antiviral agents, antiviral immunoglobulins, etc., can solve the problems of poor cure effect of severely ill bee colonies, inability of bees to eat well, and inability to directly kill viruses, etc. To achieve the effect of no drug residue, not easy to fail, and rapid action
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Embodiment 1
[0023] 1. Preparation of inactivated vaccine with oil adjuvant of Chinese bee cystic larvae virus
[0024] The diseased larvae detected positive by RT-PCR were mixed with the phosphate buffer solution of pH 7.6 first, and 1ml of phosphate buffer solution was added to each 1g of diseased larvae, and chloroform was added to the ground mixed solution, and the volume of the above mixed solution Ratio 1:0.8, homogenate at 37°C for 10 min, then centrifuge at 1000 rpm for 10 min, collect the supernatant and sediment respectively; take the supernatant, add chloroform with a volume ratio of 1:0.8 to the supernatant, Shake in a water bath at 37°C for 10 min, then centrifuge at 1000 rpm for 10 min, collect the supernatant and sediment respectively, continue to treat the supernatant twice with this method, and collect the supernatant and sediment respectively; Collect together, dissolve with pH 7.6 phosphate buffer, add 1ml phosphate buffer per 1g of precipitate, then centrifuge at 1000 r...
Embodiment 2
[0031] 1. Preparation of inactivated vaccine with oil adjuvant of Chinese bee cystic larvae virus
[0032]The diseased larvae detected positive by RT-PCR were first mixed with the phosphate buffer solution of pH7.4, and 1.5 ml of phosphate buffer solution was added to every 1 g of diseased larvae, and chloroform was added to the mixed solution after grinding, and mixed with the above mixed solution Volume ratio 1:1.2, homogenate at 39°C for 8 minutes, then centrifuge at 1200 rpm for 8 minutes, collect the supernatant and sediment respectively; take the supernatant, add chloroform with a volume ratio of 1:1.2 to the supernatant , shake in a water bath at 39°C for 8 min, then centrifuge at 1200 rpm for 8 min, collect the supernatant and precipitate respectively, continue to treat the supernatant three times with this method, and collect the supernatant and precipitate respectively; Collect together, dissolve with pH7.4 phosphate buffer, add 1.5ml phosphate buffer per 1g of preci...
Embodiment 3
[0039] 1. Preparation of inactivated vaccine with oil adjuvant of Chinese bee cystic larvae virus
[0040] The diseased larvae detected positive by RT-PCR were first mixed with the phosphate buffer solution of pH7.8, and 2ml of phosphate buffer solution was added to each 1g of diseased larvae, and chloroform was added to the ground mixed solution, and the volume of the above mixed solution Ratio 1:1.5, homogenate at 40°C for 9 minutes, then centrifuge at 800 rpm for 9 minutes, collect the supernatant and sediment respectively; take the supernatant, add chloroform with a volume ratio of 1:1.5 to the supernatant, Shake in a water bath at 40°C for 9 minutes, and then centrifuge at 800 rpm for 9 minutes to collect the supernatant and sediment respectively. The supernatant continues to be treated by this method four times, and the supernatant and sediment are collected respectively; the resulting sediment is collected Together, dissolve with pH7.8 phosphate buffer, add 2ml of phosp...
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