Monoclonal antibody against GP73 protein, preparation method and application thereof
A technology of monoclonal antibody and Golgi protein, which is applied in biochemical equipment and methods, anti-animal/human immunoglobulin, and analysis by making materials react chemically, which can solve the problem of high-throughput analysis and heavy labor , deficiency and other problems, to achieve the effect of convenient quality control, high sensitivity and good specificity
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[0030] In some embodiments of the present invention, the kit further includes a standard product of Golgi protein GP73. In some embodiments of the present invention, the standard product of the GP73 protein is a full-length GP73 protein, and is in a protein protection stable solution. The GP73 standard product can be prepared through recombinant expression by means of genetic engineering, molecular biology and biochemistry. A preparation method comprises: expressing Golgi protein GP73 with Escherichia coli, and performing affinity purification by using the fusion expressed protein tag to obtain a GP73 standard product.
[0031]In some preferred embodiments of the present invention, the above kit may also contain a microtiter plate, horseradish peroxidase (HRP)-labeled polyclonal antibody and auxiliary reagents. Wherein for the enzyme-linked immunoassay kit, the auxiliary reagent may contain the chromogenic substrate tetramethylbenzidine (TMB), and for the chemiluminescence de...
Embodiment 1
[0071] Example 1: Preparation and Characterization of Monoclonal Antibodies of the Present Invention
[0072] 1) Preparation of GP73 monoclonal antibody:
[0073] a) Construction of Golgi protein GP73 recombinant antigen (immunogen):
[0074] The full sequence of the GP73 gene was artificially synthesized according to the gene sequence number AF236056. According to the multiple cloning site of the pET-15b vector, Nde I and BamH I sites were introduced at both ends. The full length of the obtained sequence is shown in figure 1 . Insert the obtained sequence into the prokaryotic expression vector pET-15b, and the pET-15b-GP73 plasmid structure map is shown in figure 2 . The recombinant plasmid was identified by Nde I and BamH I double enzyme digestion, and whether the inserted fragment was checked by 1.2% agarose gel electrophoresis. The identification results are shown in image 3 , where the first lane is M.Takara DL2,000Marker, and the second lane is the product of doubl...
Embodiment 2
[0092] Example 2: Preparation of ELISA Quantitative Detection Kit for Golgi Protein GP73
[0093] The present embodiment prepared a Golgi protein GP73 enzyme-linked immunoassay kit (96 parts) of the present invention, and its composition comprises:
[0094] 5 bottles of Golgi protein GP73 standard;
[0095] 1 piece of GP73 monoclonal antibody-coated plate (96 wells);
[0096] 1 bottle of horseradish peroxidase (HRP)-labeled GP73 polyclonal antibody, 10ml / bottle;
[0097] 1 bottle each of substrate solution A and chromogenic solution B, each 5ml / bottle;
[0098] 1 bottle of reaction termination solution, 5ml / bottle;
[0099] 1 bottle of washing buffer (20×concentrated), 50ml / bottle.
[0100] The specific operation is as follows:
[0101] 1. Preparation of Golgi protein GP73 standard:
[0102] 1) The GP73 protein used is the full-length human GP73 protein with His tag artificially synthesized in part 1) of Example 1.
[0103] 2) Packing: Dilute GP73 protein in 2% BSA solu...
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