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A method for producing canine parvovirus monoclonal antibody by high-density culture

A technology of canine parvovirus and monoclonal antibody, applied in biochemical equipment and methods, culture process, tissue culture, etc., can solve the problems of increased risk of side effects, complex downstream process, low antibody titer, etc., to reduce exogenous Effects of virus and mycoplasma contamination, simplification of downstream processes, and reduction of side reactions

Active Publication Date: 2021-03-02
哈尔滨元亨生物药业有限公司
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  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0007] In order to make up for the deficiencies in the prior art, the present invention proposes a method for producing canine parvovirus monoclonal antibody using a high-density culture method. The technology of cloning antibody cultured cells has a low density, and the titer of cultured antibodies is low. The product needs to be concentrated and serum needs to be added during the culture, which complicates the downstream process and increases the risk of side effects

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  • A method for producing canine parvovirus monoclonal antibody by high-density culture
  • A method for producing canine parvovirus monoclonal antibody by high-density culture
  • A method for producing canine parvovirus monoclonal antibody by high-density culture

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Embodiment approach

[0048] As an embodiment of the present invention, uniformly arranged stirring rods 14 are fixedly connected to the upper surface of the support plate 13; a spiral blade 15 is fixedly connected to the outer surface of each stirring rod 14;

[0049] During work, since the top surface of the support plate 13 is fixedly connected with evenly arranged stirring rods 14, the stirring rods 14 can be driven to rotate during the rotation of the support plate 13, and the stirring rods 14 can be used for cultivating in the liquid storage tank 12 during this process. The base is stirred, so that the diffusion degree of the medium can be further improved, and the nutrients in the medium are evenly distributed. Since the outer surface of the stirring rod 14 is fixedly connected with the spiral blade 15, the spiral blade 15 can be driven during the rotation of the stirring rod 14. Moving within the medium can further increase the degree of diffusion of the medium during the process, thereby pr...

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Abstract

The invention belongs to the technical field of canine parvovirus monoclonal antibody, and specifically relates to a method for producing canine parvovirus monoclonal antibody by means of high-density culture; the bioreactor includes a storage chamber and a reaction chamber; the upper surface of the reaction chamber A storage bin is fixedly connected through a slant plate; the storage bin includes a liquid storage tank and a liquid collection tank; a support plate is provided on the inner wall of the storage bin, and the support plate is an arc design; a liquid storage cover is sleeved above the liquid storage tank The outer surface of the liquid storage tank is fixedly connected with a liquid collection tank; the inner wall of the liquid storage tank is provided with uniformly arranged first through holes; the inner wall of each of the first through holes is fixedly connected with a control valve; The invention is mainly used to solve the problem of the existing bioreactor culture hybridoma cell production technology of canine parvovirus monoclonal antibody, the cultured cell density is low, the cultured antibody titer is low, the product needs to be concentrated and serum needs to be added during the culture, It complicates the downstream process and increases the risk of side reactions.

Description

technical field [0001] The invention belongs to the technical field of canine parvovirus monoclonal antibodies, in particular to a method for producing canine parvovirus monoclonal antibodies by means of high-density culture. Background technique [0002] Canine parvovirus disease (CPVD) is a viral infectious disease caused by canine parvovirus (CPV) infection. Vomiting, bloody stool, and a large decrease in white blood cells; one is non-suppurative myocarditis type, and the sick dog will die suddenly. This disease transmission speed is fast, and morbidity rate is high, and the mortality rate of puppies is as high as 70%, and the adult dog mortality rate is relatively low but the phenomenon of recessive infection is ubiquitous. In 1978, Kelly et al. first isolated CPV from dogs suffering from hemorrhagic enteritis. Subsequently, many countries and regions in the world reported the prevalence of this disease one after another. In 1982, Liang Shizhe and others first reported...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12N5/20C07K16/08C12M1/02C12M1/08C12M1/00
CPCC07K16/081C07K2317/14C12M23/34C12M23/48C12M27/02C12M29/08C12M29/14C12N2500/90C12N2511/00
Inventor 任德强张健孙博李兰叶阳张立恒宋新刚高习文阚松鹤刘文超
Owner 哈尔滨元亨生物药业有限公司