Monoclonal antibody blocking enzyme-linked immunosorbent assay (ELISA) kit and method for detecting nonstructural protein (NSP) antibody of foot-and-mouth disease virus (FMDV)

A non-structural protein, monoclonal antibody technology, applied in the biological field, can solve the problem that 3D protein cannot distinguish between infected animals and vaccine immunized animals.

Active Publication Date: 2012-09-12
LANZHOU INST OF VETERINARY SCI CHINESE ACAD OF AGRI SCI
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] Among several non-structural proteins of FMDV, 3D was the first non-structural protein used for diagnosis, but 3D antibodies were also

Method used

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  • Monoclonal antibody blocking enzyme-linked immunosorbent assay (ELISA) kit and method for detecting nonstructural protein (NSP) antibody of foot-and-mouth disease virus (FMDV)
  • Monoclonal antibody blocking enzyme-linked immunosorbent assay (ELISA) kit and method for detecting nonstructural protein (NSP) antibody of foot-and-mouth disease virus (FMDV)
  • Monoclonal antibody blocking enzyme-linked immunosorbent assay (ELISA) kit and method for detecting nonstructural protein (NSP) antibody of foot-and-mouth disease virus (FMDV)

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Embodiment 2

[0105] Kit composition

[0106] The kit consists of 8 reagents including: enzyme-labeled reaction plate, serum diluent, 25-fold concentrated washing solution, substrate solution, 100× concentrated enzyme-labeled detection antibody, stop solution, positive control serum and negative control serum, and 4 additional Zhang sealing film and instructions.

[0107] Preparation method:

[0108] 1. Antigen Coated Plates: two 96-well high-affinity ELISA plates, first coated with 6×histidine monoclonal antibody or monospecific 2C polyclonal antibody, and passed through monoclonal antibody or The 2C polyclonal antibody captures the prokaryotic expression of the foot-and-mouth disease virus 3ABC or 2C3AB non-structural protein with a histidine tag. After the enzyme plate is processed by adding a blocking stabilizer and drying, it is vacuum-sealed and stored. The storage period can reach 1.5 years.

[0109] 2. Serum Dilution Buffer: 0.01M phosphate (PBS) solution containing 10% horse seru...

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Abstract

The invention discloses a monoclonal antibody blocking enzyme-linked immunosorbent assay (ELISA) kit and a method for detecting the nonstructural protein (NSP) antibody of a foot-and-mouth disease virus (FMDV) (FMD NSP B-ELISA); the kit comprises ELISA reaction plates, serum diluent, 25 times concentrated detergent, substrate solution, 100* concentrated ELISA detecting antibody, stop buffer, positive control serum and negative control serum; the ELISA reaction plates are two 96-pore high-affinity ELISA reaction plates, firstly 6* groups of amino acid monoclonal antibody or NSP 2C polyclonal antibody, and then FMDV 3ABC or 2C3AB NSP which is expressed by pronucleus and is provided with 6* groups of amino acid labels is captured through the monoclonal antibody or the polyclonal antibody; and compared with other similar kits, the method has higher coincidence rate and higher positive serum detection rate, and is applicable to detecting the serum of cattle, sheep, pigs and other susceptible animals.

Description

technical field [0001] The invention relates to a monoclonal antibody blocking ELISA (FMDVNSP B-ELISA) kit and method for detecting nonstructural protein antibodies of foot-and-mouth disease virus, belonging to the field of biotechnology. Background technique [0002] Foot-and-mouth disease (FMD) is a severe infectious disease caused by foot-and-mouth disease virus (FMDV) infection in cloven-hoofed animals. Due to its extremely high incidence rate, which seriously affects animal husbandry production and international trade, it is highly valued by various countries. The prevention and control of foot-and-mouth disease mainly adopts the comprehensive prevention and control measures of vaccine immunization and slaughtering of infected and suspicious animals, and both vaccine-immunized animals and infected animals will produce structural protein antibodies, so it is difficult to distinguish vaccine-immunized animals from infected animals by the diagnostic method of detecting str...

Claims

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Application Information

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IPC IPC(8): G01N33/68
Inventor 卢曾军刘在新曹轶梅付元芳孙普李冬包慧芳李平花白兴文陈应理谢宝霞厍大亮
Owner LANZHOU INST OF VETERINARY SCI CHINESE ACAD OF AGRI SCI
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