A group-selective monoclonal antibody hybridoma cell line yh6 against quinolone antibiotics and its application
A hybridoma cell line and monoclonal antibody technology, applied in the field of immunochemistry, can solve the problems of inapplicable daily rapid detection of quinolone antibiotics
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Embodiment 1
[0018] Example 1 Preparation of hybridoma cell line YH6
[0019] 1. Animal immunity and serum screening
[0020] The conjugate of hapten 1 (H1) and hemocyanin (KLH) (H1-KLH) was selected as the immunogen, and the complete adjuvant was mixed with the immunogen at a volume of 1:1 for the first dose, and BALB / c was immunized by subcutaneous immunization For mice, the interval between immunizations was 4 weeks, and 7-10 days after five immunizations, the titer and inhibition of serum were measured by indirect competitive enzyme-linked immunosorbent assay, and mice with high titer and good inhibition were selected for fusion.
[0021] 2. Cell Fusion
[0022] 7 to 10 days before fusion, in RPMI-1640 medium containing 10% fetal bovine serum in 5% CO 2 Tumor cells were cultured in an incubator. Three days before the fusion, the selected mice were immunized by abdominal sprinting. On the day of fusion, the eyeballs were removed to collect blood. After the mice were killed by cervic...
Embodiment 2
[0027] Embodiment 2 Preparation and purification of the anti-quinolone antibiotic monoclonal antibody secreted by hybridoma cell line YH6
[0028] 1. Preparation of monoclonal antibodies
[0029] Select healthy BALB / c mice and inject sterile paraffin oil at a volume of 0.6 mL / mouse. After 10 days, each mouse was intraperitoneally injected with 1×10 6 hybridoma cells. After the 6th day, observe the state of the mouse every day. If the abdomen of the mouse is obviously enlarged, feels tight when touched by hands, and is unwilling to move, collect ascites; then centrifuge (6000 rpm, 12 min) to remove red blood cells and other impurities, aliquoted and stored at -20°C.
[0030] 2. Monoclonal antibody purification
[0031] Ascitic fluid was purified by octanoic acid-ammonium sulfate precipitation. Under acidic conditions, n-octanoic acid can precipitate other miscellaneous proteins in ascites except IgG immunoglobulin, then centrifuge, and discard the precipitate; then use a c...
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