A kind of African swine fever virus antibody ELISA detection kit and preparation method thereof
A technology of African swine fever virus and detection kit, which is applied in the field of immunoassay, can solve the problems of not being able to give an accurate judgment of infection in time and taking a long time, and achieve the effect of improving accuracy, improving sensitivity and high detection sensitivity
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Embodiment 1
[0033] Embodiment 1 Preparation of African swine fever virus Δp54 protein
[0034] 1. Construction of recombinant Escherichia coli engineering bacteria E.coli BL21 / pET-Δp54
[0035] The Δp54 protein gene sequence shown in SEQ ID NO.2 was sent to Suzhou Jinweizhi Biotechnology Co., Ltd. for full sequence synthesis and connected to the pET28a plasmid. The ligated plasmid was transformed into Escherichia coli BL21 (DE3), and a single clone was picked and cultured overnight in LB medium containing 100 μg / ml kanamycin. The plasmid was extracted and then sequenced and analyzed. The positive clone was the engineering bacterium E.coli BL21 / pET-Δp54.
[0036] 2. Expression of Δp54 protein
[0037] Inoculate 1ml of E.coli BL21 / pET-Δp54 strain into 100ml of LB liquid medium containing kanamycin, shake at 220 rpm at 37°C for 2 hours, lower the temperature to 28°C, and add the final concentration 0.5mmol / L IPTG solution induced culture for 12 hours. After the bacterial culture was com...
Embodiment 2
[0040] The preparation of embodiment 2 African swine fever virus p30 protein
[0041] 1. Construction of recombinant Escherichia coli engineering bacteria E.coli BL21 / pET-p30
[0042] The p30 protein gene sequence shown in SEQ ID NO.1 was sent to Suzhou Jinweizhi Biotechnology Co., Ltd. for full sequence synthesis, and connected to the pET28a plasmid. The ligated plasmid was transformed into Escherichia coli BL21 (DE3), and a single clone was picked and cultured overnight in LB medium containing 100 μg / ml kanamycin. The plasmid was extracted and then sequenced and analyzed. The positive clone was the engineering bacterium E.coli BL21 / pET-p30.
[0043] 2. Expression of p30 protein
[0044] Inoculate 1ml of E.coli BL21 / pET-p30 strain into 100ml of LB liquid medium containing kanamycin, shake at 220 rpm at 37°C for 2 hours, lower the temperature to 28°C, and add the final concentration 0.5mmol / L IPTG solution induced culture for 12 hours. After the bacterial culture was comp...
Embodiment 3
[0047] The preparation of embodiment 3 African swine fever virus ELISA antibody detection kit
[0048] 1. Microplate preparation
[0049] Enzyme plate coating antigen: the African swine fever virus Δp54 protein and p30 protein prepared in Example 1 and Example 2 were coated with the components corresponding to the original number as shown in Table 1 with carbonate buffer solution of pH 9.6 Prepare with the coating amount, coat the ELISA plate, seal the plate with a plate sealing film, and coat at 2-8°C for 16-24 hours. Discard the liquid in the well, wash once with washing solution, 300 μl / well, and pat dry on absorbent paper.
[0050] Table 1 Coating raw components and their contents corresponding to each kit
[0051]
[0052] Blocking: 150 μl of phosphate buffer (pH 7.4) containing 20% newborn bovine serum was added to each well to block at 2-8° C. for 16-24 hours. Dry in an environment at 18-26°C and relative humidity below 30% for 3-6 hours;
[0053] Sample diluen...
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