A special diluent for alkaline phosphatase antigen antibody
An antigen-antibody and phosphatase technology, applied in the field of medicine, can solve the problems of low stability, technical difficulties, endangering the accuracy of test results, etc., and achieve the effects of reduced production cost, simple components and good hydrophilicity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0017] A special diluent for alkaline phosphatase antigen antibody, including the following components by mass fraction: 92% phosphate buffer solution, 1% polymer hydrophilic compound, 0.2% sodium edetate, and 0.01% theophylline , modified amino acid 1%, anticoagulant 0.02%, silk protein 0.05%, nano silver powder 5.72%.
[0018] The above-mentioned phosphate buffer solution includes the following components by weight: 10 parts of sodium chloride, 2 parts of potassium chloride, 25 parts of potassium phosphate, and 100 parts of deionized water. The polymer hydrophilic compound is formed by condensation of hexane oxide, chitosan and polyethylene glycol, and the molar ratio of hexane oxide, chitosan and polyethylene glycol is 2:1:3.
[0019] Wherein, the preparation method of the modified amino acid is as follows: after dissolving the dopamine solution, adding the amino acid and stirring evenly, then adding titanium dioxide powder, continuing to stir, and spray-drying at 50° C. to...
Embodiment 2
[0023] A special diluent for alkaline phosphatase antigen antibody, including the following components by mass fraction: 93% phosphate buffer solution, 1.5% polymer hydrophilic compound, 0.3% sodium edetate, and 0.015% sodium azide %, modified amino acid 2%, anticoagulant 0.03%, silk protein 0.1%, nano silver powder 3.055%.
[0024] The phosphate buffer solution comprises the following components by weight: 12 parts of sodium chloride, 3 parts of potassium chloride, 45 parts of potassium phosphate, and 180 parts of deionized water.
[0025] Wherein, the polymer hydrophilic compound is formed by condensation of hexane oxide, chitosan and polyethylene glycol, and the molar ratio of hexane oxide, chitosan and polyethylene glycol is 3:1:4.
[0026] The preparation method of the modified amino acid is as follows: after dissolving the dopamine solution, adding the amino acid and stirring evenly, then adding titanium dioxide powder, continuing stirring, and spray drying at 60° C. to ...
Embodiment 3
[0030] A special diluent for alkaline phosphatase antigen antibody, including the following components by mass fraction: 93% phosphate buffer saline, 1.9% polymer hydrophilic compound, 0.4% sodium edetate, citronella extract 0.02%, modified amino acid 1.9%, anticoagulant 0.03%, silk protein 0.07%, nano silver powder 2.68%.
[0031] The phosphate buffer solution comprises the following components by weight: 16 parts of sodium chloride, 5 parts of potassium chloride, 50 parts of potassium phosphate, and 200 parts of deionized water.
[0032] The polymer hydrophilic compound is formed by condensation of hexane oxide, chitosan and polyethylene glycol, and the molar ratio of hexane oxide, chitosan and polyethylene glycol is 4:2:5.
[0033] Wherein, the preparation method of the modified amino acid is as follows: after dissolving the dopamine solution, adding the amino acid and stirring evenly, then adding titanium dioxide powder, continuing stirring, and spray-drying at 65° C. to o...
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