Hybridoma cell strain 6B1, foot-and-mouth disease A type virus resisting monoclonal antibody secreted from hybridoma cell strain 6B1, and application of antibody
A hybridoma cell line and monoclonal antibody technology, which is applied in the application field of monoclonal antibody against foot-and-mouth disease type A virus, detection of foot-and-mouth disease type A virus antibody and antigen, and can solve complex operations, biological transmission risks, and specific detection results To avoid problems such as poor performance and achieve high-sensitivity detection and broad application prospects
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Embodiment 1
[0038] Embodiment 1, screening and identification of hybridoma cell lines
[0039] In this embodiment, the screening method for hybridoma cell lines comprises the following steps:
[0040] 1.1. Animal immunity
[0041] 1) Basic immunization: use the antigen of foot-and-mouth disease A virus (AF72) (provided by the China Veterinary Drug Administration) as the immunogen, mix and fully emulsify with Freund's complete adjuvant (purchased from Sigma) at 200 μg / 200 μl, and inject subcutaneously at multiple points For the emulsion, each Balb / c mouse (8-12 weeks old, female, SPF grade animal culture, purchased from the Experimental Animal Center of the Academy of Military Medical Sciences) was 200 μg per injection.
[0042] 2) Booster immunization: booster immunization 2 weeks later, the adjuvant is Freund's incomplete adjuvant, also mixed at 200 μg / 200 μl, and the injection volume of each Balb / c mouse (same as the above step 1)) is also 200 μg. A second booster immunization was per...
Embodiment 2
[0074] Embodiment 2, the preparation and identification of the monoclonal antibody of anti-foot-and-mouth disease type A virus
[0075] 2.1. Preparation and purification of monoclonal antibodies
[0076] 1), using the method of inducing monoclonal antibodies in animals to prepare a large amount of monoclonal antibodies: select adult BALB / c mice (SPF grade animal culture, purchased from the Experimental Animal Center of the Academy of Military Medical Sciences), intraperitoneal inoculation of liquid paraffin, each mouse 0.5mL. After 7-10 days, hybridoma cells 6B1 of passage 16 were inoculated intraperitoneally, 1×10 per mouse 6 -5×10 6 indivual. After an interval of 7 days, the abdomen was obviously enlarged, and the ascites was collected by breaking the cervical vertebrae when the mice were unable to move.
[0077] 2) Antibody purification: centrifuge the ascitic fluid (10000r / min for 30 minutes), remove cell components and other precipitates, and collect the supernatant. ...
Embodiment 3
[0085] Embodiment 3, indirect ELISA method detects foot-and-mouth disease type A virus antibody
[0086] 3.1, detect foot-and-mouth disease type A virus antibody with the monoclonal antibody 6B1anti that embodiment 2 obtains and indirect ELISA method, detection method comprises the following steps:
[0087] 1), 6B1anti antibody-coated microtiter plate: Dilute the monoclonal antibody 6B1anti with 10mM PBS buffer solution of pH 7.0-7.4 to 4μg / mL, add 110μL to each well of the microtiter plate, and coat overnight at 4°C; Remove the coating solution, pat dry, then add 300 μL of 1% BSA (in 10 mM PBS buffer solution with pH 7.0-7.4) to each well, block at 4°C overnight, and pat dry.
[0088] 2), FMD whole virus antigen capture: the inactivated FMD type A whole virus (purchased from Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences) was diluted 1:2 with 10mM PBS buffer solution of pH 7.0-7.4, and added to each well of the microtiter plate Add 110 μL, ov...
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