VEGFR-2 resistant monoclonal antibody with human and mouse cross reaction as well as preparation method and application thereof
A VEGFR-2, monoclonal antibody technology, applied in applications, antibodies, anti-animal/human immunoglobulin, etc., can solve the problem of large market demand for biological reagents
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Embodiment 1
[0069] Example 1, Preparation and Screening of Anti-VEGFR-2 Monoclonal Antibody
[0070] Application of hybridoma technology to prepare anti-VEGFR-2 monoclonal antibody, the specific steps are as follows:
[0071] 1. Preparation of mouse immunogen and antigen for detection:
[0072] 从GenBank获取VEGFR-2基因的核苷酸片段序列(accession No.NM002253)(nucleotides975-1283)gatgtggttctgagtccgtctcatggaattgaactatctgttggagaaaagcttgtcttaaattgtacagcaagaactgaactaaatgtggggattgacttcaactgggaatacccttcttcgaagcatcagcataagaaacttgtaaaccgagacctaaaaacccagtctgggagtgagatgaagaaatttttgagcaccttaactatagatggtgtaacccggagtgaccaaggattgtacacctgtgcagcatccagtgggctgatgaccaagaagaacagcacatttgtcagggtccatgaaaaa,设计并合成上下游引物:F:5-cgggatccgatgtggttctgagtccgtctcatgg-3;R:5-cggaattctcatttttcatgaactctaacaaaggtg-3。 The total RNA was extracted from normal human umbilical endothelial vein cells, the cDNA was reverse transcribed, and the VEGFR-2 gene was amplified by PCR using the cDNA as a template and the above primer conditions.
[0073] Th...
Embodiment 2
[0090] Example 2 Identification and Application of Functional Activity of Anti-VEGFR-2 Monoclonal Antibody A8H1
[0091] 1. ELISA method for functional identification and application of A8H1
[0092] Dilute commercially available recombinant VEGFR-2 protein (purchased from American R&D Company) to 2 μg / ml with coating solution, add 100 μl to each well to coat a 96-well ELISA plate, overnight at 4°C; PBST (PBS containing 0.5% Tween20) 5% Skim milk-washing buffer blocking, incubate at 37°C for 2h; after washing with PBST 5 times, add 100μl A8H1 (2μg / ml initial concentration, 11 concentration gradient dilutions) to each well overnight at 4°C; dilute at 1:5000 Goat anti-human secondary antibody (Santa Cruz Company) 100 μl / well was added to the well, and incubated at 37°C for 1 hour; peroxidase substrate chromogenic solution was 100 μl / well, and the reaction was terminated with 2M sulfuric acid after 15 minutes at room temperature, and detected on the machine Colorimetry adopts du...
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