Salmonella enteritidis nucleic acid standard sample as well as building method and application thereof
A technology of Salmonella Enteritidis and standard sample, which is applied in the preparation of Salmonella Enteritidis nucleic acid standard sample and the application field in detecting Salmonella Enteritidis, and achieves the effect of broad market, great economic benefits and social benefits
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0051] Source of strains: The standard strains used in the preparation of Salmonella Enteritidis nucleic acid standard samples were purchased from the American Type Culture Collection, and the standard strain number of Salmonella Enteritidis is ATCC: 13076. figure 1 Process flow chart for the preparation of Salmonella Enteritidis (Salmonella Enteritidis) nucleic acid standard samples.
[0052] In this article, the experimental procedures, experimental reagent preparation and other methods related to genetic engineering operations, unless otherwise specified, refer to the "Molecular Cloning Experiment Guide".
[0053] Genomic nucleic acid extraction method:
[0054] According to GB / T4789.4-2008 [1] Carry out strain activation and enrichment culture. The DNA of the enrichment broth was extracted using Qiagen’s DNA extraction kit (Qiagen Blood & Cell Culture DNA Maxi Kit, Cat. No. 13362), and the genomic DNA was extracted according to its operating instructions. Prepare nuclei...
Embodiment 2
[0079] Certainty test
[0080] 1PCR analysis
[0081] a. Instrument: PE2400, American PE Company
[0082] b. Determination: Take the prepared nucleic acid standard sample and determine by PCR analysis:
[0083] Specific fragment invA gene PCR primers in Salmonella Enteritidis:
[0084] Forward primer: SEQ ID NO: 1 5'-gtgaaattat cgccacgttc gggcaa-3'
[0085] Reverse primer: SEQ ID NO: 2 5′-tcatcgcacc gtcaaagaac c-3′
[0086] Reaction conditions:
[0087] Pre-denaturation: 94°C, 3min;
[0088] Entering the cycle: denaturation at 94°C for 60s, annealing at 60°C for 60s, extension at 72°C for 60s, 35 cycles;
[0089] Termination of extension: 72°C, 7min;
[0090] The length of the amplified product was 284bp, and a specific gene fragment of Salmonella Enteritidis was amplified, which was confirmed to be Salmonella Enteritidis after sequencing.
[0091] 2 Real-time fluorescent PCR analysis
[0092] a. Instrument: ABI 7500 real-time fluorescent quantitative PCR analyzer
[...
Embodiment 3
[0166] The preparation of Salmonella Enteritidis nucleic acid standard sample can be widely used in various food detection kits as a positive standard control substance. The specific preparation method is as described in Example 1 above.
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