Duck parvovirus indirect ELISA (enzyme-linked immuno sorbent assay) detection reagent kit
A duck parvovirus and detection kit technology, which is applied in measuring devices, instruments, scientific instruments, etc., can solve the problems of increased feed-to-meat ratio of duck flocks, increased breeding costs, and decreased pass rate of ducks out of the market, achieving strong sensitivity, The effect of high specificity and rapid detection
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Embodiment 1
[0037] Example 1 Obtaining of Purified Recombinant Duck Parvovirus VP3 Protein
[0038] A. Extraction of viral DNA: After digesting part of the liver homogenate suspension of affected ducks, the total DNA was extracted by the phenol-chloroform method, and finally the total DNA was extracted with 50 μL ddH 2 O dissolved and stored at -20°C;
[0039] B. Design and synthesis of primers: According to the published complete genome sequence of duck parvovirus, combined with our sequencing results of multiple strains of duck parvovirus isolate VP3, a pair of primers were designed using Primer Premier 5.0 and the restriction enzyme BamHI was added and HindIII restriction site, the nucleotide sequence of F1:5'-CGGATCCAAGGAAGTCACAACGCAGGAT-3' is shown in SEQ ID No.3, and the nucleotide sequence of R1:5'-CAAGCTTGCCATCAGTCTGGTATT-3' is shown in SEQ ID No.4;
[0040] C. PCR amplification: PCR reaction system: 2×EsTaqMasterMix 10 μL, upstream and downstream primers F1 / R1 (20 μmol / L) 1 μL e...
Embodiment 2
[0045] Example 2 Assembly of Duck Parvovirus Indirect ELISA Detection Kit
[0046] Recombinant protein coating: Quantitatively measure the concentration of the purified recombinant protein, take an appropriate amount of recombinant protein and mix it in 10mL 1×carbonate buffer to make the final concentration 1.5ng / L, and then add it to the bottom of the 96-well enzyme plate , 100 μL per well. Cover with sealing film and incubate overnight at 4°C.
[0047] The kit includes the following reagents: 1 piece of 96-well ELISA plate, 20mL of 30×PBST washing solution, 10mL of 1×carbonate buffer (PH=9.6), 2.5g of skim milk powder, 10mL of GoatAnti-DuckIgG-HRP, soluble type One-component TMB substrate chromogenic solution 10mL, stop solution (3mol / LH 2 SO 4 ) 10mL, 4 sheets of sealing film. Store at 2-8°C for 6 months
[0048] The components and proportions of the coating solution, washing solution, blocking solution, sample diluent, chromogenic solution and stop solution are as fo...
Embodiment 3
[0056] The usage method of embodiment 3 duck parvovirus indirect ELISA detection kit
[0057] The specific steps of the method of use are as follows:
[0058] 1. ELISA detection procedure
[0059] (1) Coat the ELISA reaction plate with 150ng / well recombinant duck parvovirus VP3 protein, incubate overnight at 4°C, and wash the ELISA reaction plate 3 times with PBST;
[0060] (2) Seal the ELISA reaction plate with 5g / 100mL skimmed milk powder solution, at 37°C, after blocking for 1 hour, wash the ELISA reaction plate 3 times with PBST;
[0061] (3) Dilute the serum to be tested 1:10 times w / v with 5g / 100mL skimmed milk powder solution, add 100 μL to the ELISA reaction plate, and after 1.5 hours at 37°C, wash the ELISA reaction plate 3 times with PBST;
[0062] (4) Add goat anti-duck IgG-HRP to the ELISA reaction plate at 100 μL / well, and after 1 hour at 37°C, wash the ELISA reaction plate 3 times with PBST;
[0063] (5) Add 100 μL of substrate color development solution to th...
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