Anti-human glycosphingolipid Globo-H monoclonal antibody and preparation method and application thereof
A technology of monoclonal antibody and glycosphingolipid, which is applied in the field of monoclonal antibody to achieve the effect of strong specific binding ability
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Embodiment 1
[0029] Example 1 Separation, purification and enrichment of glycosphingolipid Globo-H
[0030] (1) Extraction of glycosphingolipid Globo-H from tumor tissue of patients with liver cancer:
[0031] Take the liver cancer tissue sample and grind it into pieces, add the solvent chloroform:methanol (1:1, v / v) and ultrasonically shake for one hour, then centrifuge to get the supernatant, repeat four times, then add isopropanol:hexane:first-grade water ( 55:25:20, v / v / v) After ultrasonic vibration for one hour, centrifuge to get the supernatant, repeat four times, and dry in a centrifugal desiccator.
[0032] (2) Separation of neutral lipids in tumor tissues of patients with liver cancer:
[0033] First put the SephadexA25 gel solution into the column, and then equilibrate it with chloroform:methanol:water (30:60:8, v / v / v) solution, then add the dried lipid sample in step (1) to the chromatography column, and use Chloroform:methanol:water (30:60:8, v / v / v) eluted to obtain neutral g...
Embodiment 2
[0038] Example 2 Glycosphingolipid Globo-H immunized mice
[0039] Inject mice with 50 μg glycosphingolipid Globo-H combined with 0.5 mL Freund’s complete adjuvant in the intraperitoneal cavity, immunize mice again with 50 μg glycosphingolipid Globo-H combined with 0.5 ml Freund’s incomplete adjuvant after 2 weeks, and 400 μg glycosphingolipid after 4 weeks Mice were immunized intraperitoneally with lipid Globo-H. Blood was collected from the retroorbital canthus vein, and the serum was frozen at -20°C. After 4 days, the mice were sacrificed to obtain the spleen for cell fusion.
Embodiment 3
[0040] Example 3 Glycosphingolipid Globo-H immunization induces specific serum antibodies:
[0041] After immunizing mice with glycosphingolipid Globo-H three times, the anti-glycosphingolipid Globo-H antibody induced in its serum was detected by conventional ELISA method: 15 μg / mL glycosphingolipid Globo-H was dissolved in the coating solution (0.1 NaCO3, PH9.6, 0.1% BSA) coated in 96-well ELISA plate at 4°C, blocked with 5% milk-PBS; add 1:100 diluted serum in turn, HRP-labeled goat anti-mouse IgG, OPD, color development stop , measured OD490nm, showing the successful induction of specific serum antibodies.
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