Antibody capable of binding to AAV1-13
An antibody, H-CDR3 technology, applied in the field of immunology, can solve the problems of low recovery efficiency and harsh conditions, and achieve the effects of high affinity, good specificity, convenient separation and identification
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Embodiment 1
[0052] Example 1 Preparation of Antibody
[0053] Based on the VP1 of AAV8, compare AAV1-13, remove most of the non-homologous sequences to obtain the VPx sequence, construct it on the pET-21 vector, express and purify the representative, and use it as an antigen to obtain the mouse monoclonal antibody .
[0054] 1. Antigen overexpression prokaryotic vector construction
[0055] (1) Digest the plasmid pET-21(a)+-P24 with Nde1 and Xho I. 50μL enzyme digestion reaction system contains pET-21(a)+-P24 10ug, 10×Cutsmart (NEB) 5μL, Nde1 1μL Xho I 1μL, make up to 50μL with water, digest at 37°C for 4h, and perform 1% agarose gel electrophoresis , Cut off large fragments with a blade under ultraviolet light and recover and purify;
[0056] (2) Synthesize the VPx sequence, add Nde1 and Xho I restriction sites on the upstream and downstream, respectively, construct it into the puc19 vector, and name it puc19-VPx;
[0057] (3) Digest the plasmid puc19-VPx with Nde1 and Xho I: 50 μL e...
Embodiment 2
[0093] Example 2 Detection of Antibodies
[0094] The antibody prepared in Example 1 is VP-29 antibody after screening. After sequencing, the amino acid sequences of the heavy chain variable region and the light chain variable region are shown in SEQ ID NO: 15 and 16, respectively. Show.
[0095] 1. Detection of antibodies by Western Blot
[0096] Sample Preparation
[0097] Take 15 μL of AAV1-13 purified virus, add loading buffer at a ratio of 1:4 (loading buffer: cell fluid), mix, cook at 95°C for 5 minutes, place on a dry ice box, and then 4°C, 12000 g, centrifuge for 5 minutes.
[0098] SDS-PAGE gel preparation: use 10% separating gel and 5% stacking gel.
[0099] SDS-PAGE gel electrophoresis
[0100] a. Fix the gel plate to the inner tank of the electrophoresis device, put the fixed gel plate into the outer tank, and add an appropriate amount of 1×SDS electrophoresis buffer to the outer tank. And add electrophoresis buffer to the inner tank to just submerge the gel ...
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