Carbofuran bio-barcode immunoassay kit and application thereof
A biological barcode and immunoassay technology, which is applied in the field of Carboweil biological barcode immunoassay assay kits, can solve problems such as inability to apply Carboweil, and achieve the effects of ensuring sensitivity, facilitating operation and production, and improving sensitivity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0051] Preparation method of carbofuran biological barcode immunoassay assay kit
[0052] S11. Preparation of single-label colloidal gold probe
[0053] 1), gold nanoparticle synthesis method
[0054] Add 98mL of deionized water to the siliconized beaker respectively, and then add 2mL of 50mM chloroauric acid stock solution respectively, so that the concentration of chloroauric acid is 1mM, stir on a magnetic stirrer at 1000rpm / min, heat at 250°C, and continue to boil after the liquid boils 2min; absorb 10mL of 38.8mM trisodium citrate, quickly add it to the beaker at one time, keep the stirring speed and heating temperature constant, and continue to boil for 6min. It can be found that the color of the solution gradually changes from colorless to purple, and then into wine red. The different reducing doses of trisodium citrate are added to eventually turn into different colors. After the liquid is cooled, deionized water is used to restore the original volume, and it is store...
Embodiment 2
[0082] Kit use method of the present invention
[0083] The specific operations of the Carbofuran biological barcode immunoassay assay kit prepared in the above implementation case 1 are as follows:
[0084] S21. Take out the kit from the refrigerator at 4°C, and equilibrate at room temperature for 10 minutes;
[0085] S22. Sample extraction and purification
[0086] Weigh 10.0g (accurate to 0.01g) sample; add 10mL acetonitrile, homogenize at high speed for 0.5min, add 4.0g anhydrous MgSO 4 After mixing with 1.0g NaCl, vortex at high speed for 1 min, and centrifuge at 10,000 r / min at 4°C for 5 min at high speed. Accurately pipette 2 mL of acetonitrile extract into a 10 mL plastic centrifuge tube, add 50 mg of N-propylethylenediamine (PSA) and 50 mg of C18 solid phase dispersion extraction purifier, vortex at high speed for 0.5 min, and centrifuge at 10,000 r / min at 4°C 5min. Take 1 mL of the supernatant, blow it to dryness with nitrogen at 30°C, and dissolve the residue wi...
experiment example 1
[0094] The methodological examination result of kit of the present invention
[0095] The kit prepared in Example 1 was identified according to the common verification procedures in this field, and the results are shown in Table 1.
[0096] The methodological testing result of test kit of the present invention of table 1
[0097]
[0098] The above results show that the accuracy, specificity, precision, sensitivity and stability of the "Carbofuran Biological Barcode Immunoassay Assay Kit" are fully qualified.
PUM
Property | Measurement | Unit |
---|---|---|
particle diameter | aaaaa | aaaaa |
particle diameter | aaaaa | aaaaa |
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