Genetic bar code detection kit of dermestidae insect
A detection kit and barcode technology, which is applied in the determination/inspection of microorganisms, biochemical equipment and methods, etc., can solve the problems of insufficient system reports, achieve high amplification efficiency, simple operation, and reduce the quality of specimens. Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0028] A gene barcode detection kit for Dermestidae insects, which can quickly detect 19 kinds of dermestidae (as shown in Table 1), including at least 20 times of primer J1837 / N2110 reagent and 1 gene barcode sequence disc; primer J1837 / N2110 The N2110 sequence is as follows:
[0029] J1837 sequence: 5'-TATAGCATTCCCACGAATAAATA-3',
[0030] N2110 sequence: 5'-ATTTCGGTCAGTTAATAATATAG-3'.
[0031] The gene barcode sequence disk contains 19 kinds of 61 standard barcode sequences, and the detailed sequences are shown in SEQ ID NO.1-61.
[0032] Table 1 Dermatomid species name
[0033] serial number Chinese name Latin name 1 Small round beetle Anthrenus verbasci 2 Specimen orb beetle Anthrenus museorum 3 Carpet beetle Anthrenus scrophulariae 4 two-star fur beetle Attagenus pellio 5 Derma beetle Attagenus smirnovi 6 A species of fur beetle Attagenus woodroffei
[0034] 7 black fur beetle Attagenus unic...
Embodiment 2
[0037] Seven samples of Trogoderma zebra, Trogoderma cerevisiae, Dermoderma cerevisiae, Dermoderma spp., Beetle grandis, Bean beetle four-striped and Rice-beetle were selected as the samples to be tested. Adopt the kit detection of embodiment 1, the steps are as follows:
[0038] 1) Total DNA extraction
[0039] DNA was extracted using GenMagBio Animal Cell Tissue / Cell Genomic DNA Magnetic Beads Extraction Kit. The specific process is as follows:
[0040] Directly cut 30 mg of the feet and chest of the test specimen and put it into a 2 mm test tube. Soak the preserved specimen in absolute ethanol, rinse and soak it with sterile distilled water for 4 to 5 times, and discard the water; soak the dry specimen in sterile distilled water for 3 hours and blot dry. Place in a 2mL centrifuge tube, shake and grind in MM400 ball mill (30 times / s) for 30s, add 180μL Lysis Buffer, 20μL Proteinase K, shake and mix well, leave at room temperature overnight, shake and warm at 55°C for 3-5h,...
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