Loop-mediated isothermal amplification-based nucleic acid test method for Riemerella anatipestifer
A duck plague Riemer's, ring-mediated isothermal technology, applied in biochemical equipment and methods, microbial measurement/inspection, etc., can solve the problems of expensive fluorescent quantitative PCR instruments, limited popularization and use, cumbersome operation process, etc., to achieve Ease of application and promotion, simple equipment requirements, and the effect of reducing pollution
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
example 1
[0022] 1. Test samples: Riemerella anatipestifer ATCC 11845, Escherichia coli O46, Staphylococcus aureus ATCC6538, Pasteurella multocida CVCC493, Salmonella CMCC 50083.
[0023] 2. Nucleic acid extraction: In the present invention, the sample DNA extraction methods include two methods.
[0024] Method 1: Phenol imitation extraction hair method
[0025] (1) Riemerella anatipestifer was cultured in tryptic soybean broth at 37°C for 24 hours with shaking in a water bath, and Escherichia coli, Staphylococcus aureus, Pasteurella multocida, and Salmonella were cultured in LB broth for 24 hours with shaking in a water bath at 37°C;
[0026] (2) Take 500 ul of the bacterial suspension from the above-mentioned bacterial suspension and put it in the EP tube (the throat swab is soaked with 500 ul of normal saline to get the immersion solution, and various tissues of dead ducks are homogenized with 500 ul of normal saline to get the homogenate) Centrifuge at 1000rpm for 5min, discard the...
example 2
[0046] 1. The Riemerella anatipestifer ATCC 11845 bacterium liquid of overnight culture is diluted 10 times to (10 1 -10 8 ), take each 100ul plate count of each dilution bacterial solution. The number of colonies per milliliter of the stock solution was measured to be 4.0x10 8 CFU / mL, after 10-fold dilution, nucleic acid was extracted according to the pyrolysis method in Method 2 above, and 1ul of the supernatant was used as a template for LAMP amplification.
[0047] 2. The reaction composition system of Riemerella anatipestifer LAMP detection is as follows:
[0048] 2xU-LAMP reaction mixture (2xU-LAMP reaction mixture is a purchased kit, which consists of: 40mM Tris-HCl (pH 8.8), 20mM KCl, 20mM (NH4) 2 SO 4 , 10mM MgSO 4 , 0.2% Triton X-100, 2.4mM dNTPs, 1.6M betaine;) 10ul;
[0049] 10x primer mixture 1ul, its composition is: primer F3 is 2uM, primer B3 is 2uM, primer BIP is 12uM, primer FIP is 12uM;
[0050] Template DNA 1ul, Bst polymerase 0.75ul, water up to 20ul...
example 3
[0054] 1. Take 10 livers of ducks artificially infected with Riemerella anatipestifer and 20 heart, liver and brain tissues of suspected Riemerella anatipestifer sent for inspection from different regions in Sichuan, Chongqing, Shandong, and Henan provinces for implementation Nucleic acid extraction method one (phenol imitation extraction hair method) method extracts nucleic acid in the example 1, is compared with the same treatment of normal duck liver tissue simultaneously;
[0055] 2. The reaction composition system of Riemerella anatipestifer LAMP detection is as follows:
[0056] 2xU-LAMP reaction mixture (2xU-LAMP reaction mixture is a purchased kit, which consists of: 40mM Tris-HCl (pH 8.8), 20mM KCl, 20mM (NH4) 2 SO 4 , 10mM MgSO 4 , 0.2% Triton X-100, 2.4mM dNTPs, 1.6M betaine;) 10ul;
[0057] 10x primer mixture 1ul, its composition is: primer F3 is 2uM, primer B3 is 2uM, primer BIP is 12uM, primer FIP is 12uM;
[0058] Template DNA 1ul, Bst polymerase 0.75ul, wat...
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