Detection kit and detection method for brucellae in meat products
A technology for detection kits and detection methods, applied in kits and compositions used for detection, using PCR-DHPLC to detect and type 6 kinds of Brucella in meat products, which can solve the problems of easy pollution, consumption Time length, false positive and other issues, to achieve the effect of reduced detection cost, high sensitivity, and strong specificity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0060] Example 1, the establishment of Brucella detection kit and detection method in meat products
[0061] (1) Establishment of detection kit for Brucella in meat products
[0062] The inventor compares and analyzes 6 kinds of Brucella homologous sequences, and designs the universal primer pair of Brucella:
[0063] Upstream primer: 5'-TGGCTCGGTTGCCAATATTCAA-3'
[0064] Downstream primer: 5'-CGCGCTTGCCTTTCAGGTCTG-3'
[0065] On this basis, assemble a test kit for Brucella detection in meat products, which includes Taq DNA polymerase and PCR reaction solution with a concentration of 5U / μL; the PCR reaction solution contains 10mM Tris HCl, 50mM KCl, 25mM MgCl 2 , dNTP (dATP, dGTP, dCTP and dTTP) each 2.5mM and the above-mentioned Brucella universal detection primer 0.2mM.
[0066] (2) Establishment of the detection and classification detection method for Brucella in meat products:
[0067] ①Preparation of the sample to be tested: the DNA genome of the sample to be tested ...
Embodiment 2
[0100] Embodiment 2, specificity test
[0101] The DNA template library of reference strains listed in Table 1 was taken, and tested according to the method established in the examples. The test results showed that only 6 kinds of Brucella had positive absorption peaks, and the rest of the strains had no positive absorption peaks, showing high detection specificity for Brucella.
[0102]In order to confirm that this positive absorption peak is the fragment of Brucella specific gene, the present invention carries out cloning and sequencing after the positive absorption peak product of DHPLC is recovered, and the result is compared with the DNA sequence of Brucella OMP, has proved DHPLC positive The absorption peak is a fragment of OMP gene of Brucella.
[0103] The test results show that the universal PCR detection primers for Brucella can be amplified by PCR, and can specifically detect 6 kinds of Brucella of the genus Brucella under the non-denaturing analysis condition of D...
Embodiment 3
[0104] Embodiment 3, sensitivity test
[0105] According to the method for enriching bacteria established in Example 1, use the turbidimetric method to quantify the bacterial solution concentration of the compound enriched bacteria cultivated, use the method established in Example 1 to extract DNA and detect, the test results are as attached figure 2 As shown, the DHPLC peak shapes from high to low are: 2.7×10 4 CFU / mL cfu / mL Brucella; 2.2×10 3 cfu / mL Brucella; 210cfu / mL Brucella; 19cfu / mL Brucella. The results show that the detection limit of the method of the present invention can reach about 0.95pg / ul Brucella DNA, and the lower detection limit can detect about 19 Brucella.
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com