Field fast high-sensitivity detection kit and detection method for prawn hepatopancreatic parvovirus
A detection kit and parvovirus technology, which is applied in the direction of microorganism-based methods, biochemical equipment and methods, and microorganism measurement/inspection, and can solve the problems of limiting the popularization and application of PCR detection methods, difficult and rapid detection of PCR detection methods, and pathological slices In order to achieve the effect of program and standardization, shorten the preparation time, and ensure the safety of operators and the environment.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0035] Example 1: On-site Rapid and Highly Sensitive Detection Kit for Shrimp Hepatopancreatic Parvovirus
[0036] Test kit of the present invention is made up of following parts (can detect the packing of 4 samples):
[0037] (1) Sampling tubes, 4 pieces, used to hold and grind samples to be tested;
[0038] (2) Rinsing tubes, 6 pieces, each tube is equipped with 1ml of distilled water;
[0039] (3) Nucleic acid denaturation tubes, 6 pieces, each containing 20 μL of TE buffer (containing 10 mM Tris-HCl and 1 mM EDTA, pH 8.0);
[0040] (4) Amplification detection tubes, 6 pieces, each tube is equipped with 25 μL of amplification reaction solution and 1 μL of nucleic acid dye, the components of the amplification reaction solution are as follows: each of the upstream primer 1 and downstream primer 1 of the amplification primers is 1.6 μM, 0.2 μM each of upstream primer 2 and downstream primer 2 of the amplification primers, 1.4 mM each of dATP, dTFP, dGTP, and dCTP, MgCl 2 8m...
Embodiment 2
[0047] Example 2 The isothermal amplification detection method of prawn hepatopancreatic parvovirus of the present invention
[0048] Use the detection kit in embodiment 1, carry out according to the following steps:
[0049] (1) Take about 0.1 g of the sample prawn tissue and place it in the sampling tube, and quickly grind the sample to a pulp with a grinding rod;
[0050] (2) Dip the slurry sample with a grinding rod to fully wet the FTA diaphragm;
[0051] (3) Draw the quick-drying liquid onto the above-mentioned FTA membrane, and let the FTA membrane stand at room temperature for 10 minutes;
[0052] (4) Transfer the above-mentioned FTA membrane to the rinse tube with a toothpick, and shake the rinse tube vigorously for 3 minutes;
[0053] (5) Use a toothpick to transfer the FTA membrane in the above-mentioned rinsing tube to the nucleic acid denaturation tube, and incubate at 95°C for 3 minutes to allow the DNA double strands to fully melt, and then quickly place it at...
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