Monoclonal antibody for detecting human alpha-fetoprotein, kit and application
A monoclonal antibody and alpha-fetoprotein technology, applied in the biological field, can solve the problems of linear range and sensitivity that need to be further improved, lack of clinical application value, inability to develop and produce kits, and achieve good detection results
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Embodiment 1
[0049] The preparation of embodiment 1 monoclonal antibody
[0050] Antigen human alpha-fetoprotein (Human Myoglobin) was purchased from Guilin Inmate Biotechnology Co., Ltd., isolated and purified from human umbilical cord blood, and its concentration was 7.6mg / ml. composed of amino acid residues. hAFP is a multifunctional transporter that is highly expressed in the fetus and silenced after birth. Serum hAFP concentration is a direct or indirect evaluation index of many diseases, especially common in prenatal diagnosis and liver cancer diagnosis and condition monitoring.
[0051] The preparation method of anti-human alpha-fetoprotein mouse monoclonal antibody is as follows:
[0052] (1) Animal immunity
[0053] 1) Initial immunization: 30 μg of antigen plus an equal volume of complete Freund's adjuvant is fully emulsified and injected subcutaneously into mice at multiple points;
[0054] 2) Secondary immunization: 2 weeks later, the same amount of antigen as the first imm...
Embodiment 2
[0095] The specificity analysis of embodiment 2 monoclonal antibody
[0096] The four important monoclonal antibodies Ab 1-A b 4 screened above all have very high affinity to the immunogen hAFP. In order to further identify their specificity and verify whether they can specifically bind to naturally occurring hAFP, they were tested in cells The following two experiments were designed at the level and organizational level.
[0097] 1) Immunofluorescence staining of HepG2 human liver cancer cells
[0098]It is known that human liver cancer cells HepG2 can synthesize a large amount of hAFP in the cells, and the four monoclonal antibodies Ab1-Ab 4 were used for cell fluorescence staining experiments.
[0099] Experimental method: ① One day before the experiment, take HepG2 cells in good condition to make a cell suspension, and count the cells at a cell concentration of 5×10 5 Place the amount of cells / well into the wells of a six-well plate with coverslips placed; ②Cultivate in ...
Embodiment 3
[0110] Example 3 Sequence and structure analysis of monoclonal antibodies Ab1-Ab4
[0111] Further sequence and structural analysis of the obtained monoclonal antibodies Ab 1, Ab 3, and Ab 4 revealed that the variable regions of Ab 1, Ab 3, and Ab 4 all include a heavy chain variable region and a light chain variable region.
[0112] (1) From the perspective of gene sequence:
[0113] The gene sequence of the heavy chain variable region of the monoclonal antibody Ab1 is shown in SEQ ID NO.1, and the gene sequence of the light chain variable region is shown in SEQ ID NO.2;
[0114] The gene sequence of the heavy chain variable region of the monoclonal antibody Ab3 is shown in SEQ ID NO.3, and the gene sequence of the light chain variable region is shown in SEQ ID NO.4;
[0115] The gene sequence of the heavy chain variable region of the monoclonal antibody Ab4 is shown in SEQ ID NO.5, and the gene sequence of the light chain variable region is shown in SEQ ID NO.6.
[0116] (...
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