Hybridoma cell strain secreting gamithromycin monoclonal antibody and application of hybridoma cell strain
A technology of hybridoma cell lines and monoclonal antibodies, which is applied in the direction of analysis materials, biochemical equipment and methods, and material inspection products, can solve the problems of long detection time, inapplicability to rapid detection of a large number of samples, and complex processing, etc., to achieve good results Effect of Assay Sensitivity and Specificity
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Embodiment 1
[0044] Example 1: Synthesis of Gamithromycin Hapten
[0045] Since the small molecule of gaminomycin is not immunogenic and cannot stimulate the immune response of mice to produce antibodies, it is necessary to couple gaminomycin to the protein through protein linkage technology to obtain immunogenicity; protein Active groups commonly used in coupling techniques include amino, carboxyl, hydroxyl, mercapto, etc. Since the molecular structure of gamithromycin does not contain amino, carboxyl, and contains many hydroxyl groups, its analogues were found to derive carboxyl groups.
[0046] The derivatized gamithromycin hapten structure of the present invention is as follows:
[0047] .
Embodiment 2
[0048] Example 2: Synthesis of Gamimycin Complete Antigen
[0049] Weigh 4.0mg gamithromycin hapten (GAM-COOH), 3.1mg N-hydroxysuccinimide (NHS), dissolve in 300μL N,N-dimethylformamide (DMF), stir at room temperature for 10min ; Then weigh 4.9 mg 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC), fully dissolve it with 100 μL DMF, add it to the GAM-COOH solution, and stir at room temperature Reaction 4-6h (called A solution). Take 6mg KLH, dilute it to 3mg / mL with 0.01M carbonate buffer solution (CBS) (called solution B), then slowly add solution A to solution B drop by drop, react at room temperature overnight; then use 0.01M PBS solution Dialyze to remove the unreacted small molecule hapten to obtain the complete antigen GAM-COOH-KLH, which is identified by the ultraviolet absorption scanning method.
Embodiment 3
[0050] Embodiment 3: the synthesis of gamimycin coating former
[0051] Dissolve 4.2mg gamithromycin hapten (GAM-COOH) and 2.3mg N-hydroxysuccinimide (NHS) in 300μL anhydrous N,N-dimethylformamide (DMF), and stir at room temperature for 10min , to obtain gamimycin hapten (GAM-COOH) solution; 3.8 mg 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC) was dissolved in 100 μL anhydrous DMF Finally, add it to the GAM-COOH solution, stir at room temperature and react for 4-6 hours to obtain liquid A; dilute 6 mg of chicken ovalbumin (OVA) with 1 mL of carbonate buffer solution (CBS) with a concentration of 0.01 mmol / L to obtain Solution B; slowly add solution A to solution B dropwise for reaction to obtain a reaction solution; dialyze the reaction solution with PBS solution to remove unreacted small molecule haptens to obtain the coating original (GAM-COOH-OVA).
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