LAMP primer for detecting tilapia parvovirus and application thereof
A parvovirus, tilapia technology, applied in DNA/RNA fragments, microorganisms, recombinant DNA technology, etc., can solve the problems of tilapia breeding and export economic losses, tilapia death, etc., to ensure high specificity, The method is fast and simple, and the effect of improving the detection efficiency
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0018] A kind of tilapia parvovirus TiPV, its isolation process is as follows:
[0019] 1) Take out and grind the tilapia spleen, kidney and other tissues carrying the virus, dilute the medium by 100 times, centrifuge at 2000rpm, take the supernatant and filter, inoculate into a single layer of tilapia kidney cell line (Tilapia Kidney, TiK), After culturing at 25°C for 7 days, cytopathic effect (CPE) occurred. It can be seen that the TiK cells shrank and became round, the refractive index increased, some cells began to fall off, and the cell monolayer began to rupture.
[0020] Medium: M199, 10% fetal bovine serum, pH 7.0-7.2
[0021] 2) Collect the diseased cells, and use transmission electron microscopy for morphological identification.
[0022] 3) The virus is collected and sequenced to obtain the specific gene of tilapia parvovirus TiPV, which is shown in SEQ ID NO.1.
[0023] Morphological characteristics of tilapia parvovirus: the virus is spherical, and the virus has ...
Embodiment 2
[0025] Primers designed based on the difference between the specific gene of tilapia parvovirus TiPV (shown in SEQ ID NO.1) and other viral genes:
[0026] A detection primer for tilapia parvovirus TiPVLAMP, including F3: 5'-CAACTAAAGACCCGGTTCC-3', B3: 5'-GCCTTGGTAGCGTAAGTTCA-3'; FIP: 5'-GCTATCTCCTCGTTGCTCGGTG-ATCCAGCAATTCCGGAGACA-3', BIP: 5'-AGGACGGCCCGGAAGTACTG -TCAAATCCGAGCTGTGTAGC-3'.
Embodiment 3
[0028] Utilize tilapia parvovirus TiPV LAMP to detect primers to the detection of tilapia parvovirus, the method comprises:
[0029] 1. Extraction of total DNA from tilapia tissues or infected cells: Omega (USA) DNA extraction kit was used to extract tissue DNA.
[0030] 2. LAMP reaction amplification:
[0031] Use 25μl reaction system: including: inner primers FIP and BIP each 0.8μM, outer primers F3 and B3 each 0.1μM, dNTPs1mM, Betaine 0.5M, DTT 4mM, MgCl 2 8mM, Bst DNA polymerase 8U, AMV reverse transcriptase 5U, template RNA 5μl, 1×ThermoPol Reaction Buffer. After the reaction tube was incubated at 65°C for 60 minutes, it was inactivated at 80°C for 2 minutes.
[0032] F3: 5'-CAACTAAAGACCCGGTTCC-3',
[0033] B3: 5'-GCCTTGGTAGCGTAAGTTCA-3';
[0034] FIP: 5'–GCTATCTCCTCGTTGCTCGGTG-ATCCAGCAATTCCGGAGACA-3',
[0035] BIP: 5'-AGGACGGCCCGGAAGTACTG-TCAAATCCGAGCTGTGTAGC-3'.
[0036] LAMP reaction amplification product analysis:
[0037] 1. Take 5 μL of the amplified product,...
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