Marine animal and human pathogenic bacteria-bacteriolysis vibrion gene diagnostic reagent kit and detecting method
A technology for marine aquatic products and vibrio alginolyticus, which is applied in biochemical equipment and methods, measurement/testing of microorganisms, resistance to vector-borne diseases, etc., and can solve problems such as limited application and development, troublesome preparation, and low specificity , to achieve the effect of avoiding the spread of germs, ensuring rapidity and high practical value
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0030] Embodiment 1: the genetic diagnosis kit of Vibrio alginolyticus
[0031] The kit consists of the following parts (10 samples):
[0032] 1). Sample diluent (solution A), 1 tube, 5ml / tube, filled with 1×PBS, pH7.4.
[0033] 2).PCR reaction solution (solution B), 1 tube, 250μl / tube, containing PCR amplification reaction solution (25μl system), including ddH 2 O, containing Mg 2+ 10×Buffer, dNTP, primer VaF, primer VaR and TaqE.
[0034] 3). Positive control solution (solution C), 1 tube, 20 μl / tube, containing the total DNA of Vibrio alginolyticus, as a positive template;
[0035] 4). Cuboid box, 8.5×5.8×6.2cm 3 .
[0036] 5). A piece of foam board, the same size as the bottom of the box, 2.2cm high, four rows of holes, the first row of four holes, the hole diameter is 1.3cm, the second row of five holes, the hole diameter of 1.0cm, the third and fourth There are six holes in each row, and the hole diameter is 0.6cm. The above-mentioned small tubes are respectively ...
Embodiment 2
[0047] Embodiment 2: Detection method of marine aquatic animals and human pathogen-Vibrio alginolyticus
[0048] Use the test kit of embodiment 1, carry out according to the following steps:
[0049] 1). Using aseptic method, take 0.05 g of fresh abalone liver tissue, add 500 μl of sample diluent (liquid A) to dilute 10 times, and homogenize in an ice bath in a sterile homogenizer;
[0050] 2). Centrifuge at 6000r / min for 5min;
[0051] 3). Take 100 μl of the supernatant, boil for 15 minutes, and immediately put it on ice for 5 minutes;
[0052] 4). Centrifuge at 6000r / min for 10min, and use the supernatant as a PCR template;
[0053] 5). Take 1 μl of the template and solution C respectively, add it to the PCR reaction solution (solution B), centrifuge at 1000r / min for 10sec after mixing, and place it on the PCR instrument;
[0054] 6). Amplify according to the following conditions:
[0055] Pre-denaturation at 95°C for 3min→34 cycles at 94°C for 1min→10min at 72°C→storage a...
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