Haemophilus parasuis detection kit and detection method thereof
A technology of Haemophilus suis and detection kit, applied in the field of molecular biology, can solve the problems of poor specificity, need to improve sensitivity, complicated operation, etc., and achieve the effects of high sensitivity, short time consumption and accurate detection
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0040] 1. Preparation of DNA template:
[0041] For liquid culture, take Haemophilus parasuis LC strain and centrifuge at 10,000r / min for 5min, discard the supernatant, resuspend in sterilized water, boil in boiling water for 10min, freeze at -20°C, and centrifuge at 10,000r / min after thawing After 5 min, the supernatant was taken as a DNA template.
[0042] Solid culture Pick several colonies and suspend them in 100 μL sterilized water, mix them by blowing and aspiration, boil in boiling water for 10 minutes, freeze at -20°C, after thawing, centrifuge at 10,000 r / min for 5 minutes, and take the supernatant as a DNA template.
[0043] 2. Primer Design
[0044] According to GenBank published HPS mviN gene sequence (CP001321.1), two pairs of specific primers were designed and sent to Shanghai Sangon Bioengineering Technology Service Co., Ltd. for synthesis. The sequences of PCR primer pairs are shown in Table 1.
[0045] Table 1 PCR primer pair sequences
[0046]
[004...
Embodiment 2
[0065] The kit with good specificity and high sensitivity in Example 1 was used to detect Haemophilus parasuis in dead animal tissues and blood samples.
[0066] 1. Preparation of DNA template:
[0067] The dead pig No. 1 that died after the disease and the dead pig No. 2 that was not sick were prepared as DNA templates respectively. The specific preparation method is as follows: take heart, lung, and lymph nodes, add PBS to grind, incubate at room temperature for 10 minutes, centrifuge at 5000 r / min for 5 minutes, and take supernatant for tissue DNA extraction. Blood clots are discarded first, and the liquid is taken for DNA extraction. Add 50 μL of 10% SDS solution and 10 μL of 20ug / ml proteinase K to 500 μL of tissue supernatant or blood, and bathe in water at 56°C for 2 hours; add 500 μL of Tris saturated phenol, mix well, and centrifuge at 12,000 r / min for 15 minutes; take the supernatant, Add an equal amount of Tris saturated phenol: chloroform: isoamyl alcohol (25:24:...
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