Monoclonal antibodies against duck Tembusu virus, antigen detection kit and application
A duck Tembusu virus and monoclonal antibody technology, which is applied in the field of animal virology and immunology, can solve the problems of long detection period, cumbersome operation, and inability to detect, and achieve the effect of short detection time, high sensitivity and rapid detection
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Embodiment 1
[0032] Example 1 Preparation and Identification of Duck Tembusu Virus Monoclonal Antibody
[0033] The present invention accidentally obtained three hybridoma cell lines with high titer and good specificity through a large number of screening work, which were respectively named duck Tembusu virus monoclonal antibody hybridoma cells 1D4, 3F2 and 3B4, and were released on August 26, 2013. It was sent to the Beijing China General Microorganism Culture Collection Management Center (CGMCC) for preservation (Address: No. 3, Datun Road, Chaoyang District, Beijing, Institute of Microbiology, Chinese Academy of Sciences, Zip Code 100101), classified as hybridoma cells, and its preservation The numbers are CGMCC NO:8104, CGMCC NO:8107, and CGMCC NO:8106. The acquisition and detection of the three monoclonal antibodies are described in detail below.
[0034] . Preparation of Duck Tembusu Virus Antigen
[0035] 1.1 Preparation of virus
[0036] The DTMUV-JXSP strain virus was prop...
Embodiment 2
[0060] Example 2 Establishment of Double Antibody Sandwich ELISA Antigen Detection Method for Duck Tembusu Virus
[0061] 1. Establishment of double-antibody sandwich ELISA antigen detection method for duck Tembusu virus
[0062] 1) Coating: dilute anti-DTMUV monoclonal antibody 100 μL / well with 0.05mol / LPH9.6 carbonate buffer, and coat overnight at 4°C;
[0063] 2) Washing: Dry the liquid in the wells of the plate, wash with washing liquid four times, each time for 4 minutes;
[0064] 3) Blocking: add blocking solution, i.e. sample diluent, 200 μL / well, block at 37°C for 2 hours;
[0065] 4) Washing: Dry the liquid in the wells of the plate, and wash with washing liquid four times, each time for 4 minutes;
[0066] 5) Add antigen: Antigen is properly diluted with sample diluent, 100 μL / well, incubated at 37°C for 1 hour;
[0067] 6) Washing: Dry the liquid in the wells of the plate, and wash with washing liquid four times, each time for 4 minutes;
[0068] 7) Add enzy...
Embodiment 3
[0095] Example 3 Assembly of Duck Tembusu Virus Double Antibody Sandwich ELISA Antigen Detection Kit
[0097] 96-well ELISA plate coated with anti-Duck Tembusu virus monoclonal antibody 3B4;
[0098] Standard positive control: Tambusu virus DTMUV antigen;
[0099] Standard negative control: BHK cell protein;
[0100] (4) Antibody 3F2 labeled with horseradish peroxidase;
[0101] ⑸ Washing liquid: NaCl 0.8g, KH 2 PO 4 0.27g, Na 2 HPO 4 . 12H 2 O 1.42g, KCl 0.2g, Tween20 0.5mL, add double distilled water to 1000mL;
[0102] ⑹ Sample diluent (blocking solution): NaCl 0.8g, KH 2 PO 4 0.27g, Na 2 HPO 4 . 12H 2 O 1.42g, KCl 0.2g, BSA 10g, add double distilled water to 1000ml;
[0103] ⑺ Substrate solution A: 3, 3’, 5’, 5-tetramethylbenzidine diamine (TMB) 200mg, absolute ethanol 100ml, add double distilled water to 1000ml;
[0104] ⑻ Substrate solution B: Na 2 HPO 4 14.6g, citric acid 9.3g, 0.75% hydrogen peroxide ur...
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