AFP-antigen-based AFP nanobody A18
A nano-antibody and antigen technology, applied in the biological field, can solve the problems of expensive antibody and antigen standard products, and achieve the effects of small molecular weight, good specificity and cost saving
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Embodiment 1
[0022] Example 1. Construction of camel-derived immune single domain heavy chain antibody library
[0023] 1) Immunity of alpacas:
[0024] A healthy adult alpaca was selected and immunized by intradermal and subcutaneous multi-point injections on the back. For the first immunization, Freund's complete adjuvant was used, and the dose of immunogen was 1 mg; on the 28th day, the second immunization was performed with Freund's incomplete adjuvant. The dose of immunogen is 0.5 mg, three immunizations on the 49th day, Freund's incomplete adjuvant, the immunogen dose is 0.25 mg; on the 70th day, four immunizations, Freund's incomplete adjuvant, the immunogen dose is 0.25 mg. On the seventh day after the third booster immunization, the peripheral blood of the alpaca was collected for the construction of a phage display library.
[0025] 2) Separation of camel-derived white blood cells: add lymphocyte separation solution to the centrifuge tube, then add blood samples, centrifuge at 7...
Embodiment 2
[0049] Example 2. Affinity panning and identification of AFP Nanobodies
[0050] 1) Affinity panning of AFP Nanobody: In the first round of panning, the anti-AFP antigen was diluted with PBS (pH 7.4), and coated with a microtiter plate at a final concentration of 100 μg / mL, and kept at 37° C. for 2 hours. After washing 4 times with PBST (10 mM PBS, 0.5% Tween-20 (v / v)), 300 μL of 3% OVA-PBS was added to block for 1 hour at 37°C. After 1 hour, the blocking solution was discarded, washed 10 times with PBST, and 100 μL camel-derived immune single-domain heavy chain antibody library (titer about 1.0×10 11 cfu), incubated at 37°C for 1 hour. Aspirate unbound phage, wash with PBST 10 times, add 100 μL of Glycine-HCl (0.2M, pH 2.2) to elute for 8-10 min, and immediately neutralize with 15 μL of Tris-HCl (1M, pH 9.1). Take 10 μL of the eluted phage to determine the titer, and the rest is used to infect 20 mL of E.coli TG1 strain grown to the logarithmic phase for amplification. The...
Embodiment 3
[0061] Example 3. The sequencing of the gene encoding the AFP Nanobody and the determination of its amino acid sequence
[0062] The positive phage clones identified by double-antibody sandwich ELISA were subjected to DNA sequencing, and the amino acid sequence could be obtained according to the DNA sequencing results and the codon table.
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