Biological protein two-dimensional nano-film prepared by using lysozyme and preparation method of biological protein two-dimensional nano-film
A two-dimensional nano and protein technology, applied in the direction of nanotechnology, can solve the problems of difficult realization of macroscopic organization and complex synthesis route, and achieve the effect of simple preparation method and environmental friendliness
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0025] Add 0.1433g of tris(2-carboxyethyl)phosphine into 10mL of 10mmol / L tris(2-carboxyethyl) buffer solution with a pH value of 7.4, adjust the pH value to 5.0 with NaOH, and prepare 50mmol / L of tris(2-carboxyethyl) Tris buffer solution of phosphine; add 20mg lysozyme to 10mL10mmol / L tris buffer solution with pH value of 7.4, and prepare tris buffer solution of 2mg / mL lysozyme Buffer solution; mix 10mL of 50mmol / L tris(2-carboxyethyl)phosphine tris buffer solution with 10mL 2mg / mL lysozyme tris buffer solution, and let stand at room temperature for 50 minutes , forming a thin film on the surface of the mixture (such as figure 1 Shown), that is, biological protein two-dimensional nano film, its thickness is about 50nm. Depend on figure 2 and image 3 It can be seen that the two-dimensional nano-film of biological protein is formed by the self-assembly of nanoparticles with a particle size of about 30nm-50nm generated during the phase transition process.
Embodiment 2
[0027] Add 0.1147g of tris(2-carboxyethyl)phosphine into 10mL of 10mmol / L tris(2-carboxyethyl) buffer solution with a pH value of 7.4, adjust the pH value to 5.0 with NaOH, and prepare 40mmol / L of tris(2-carboxyethyl) base) Tris buffered solution of phosphine; 50mg lysozyme was added into 10mL10mmol / L pH value of 7.4 Tris buffered solution to prepare 5mg / mL Tris of lysozyme Buffer solution: Mix 10mL of 40mmol / L tris (2-carboxyethyl) phosphine tris buffer solution with 10mL 5mg / mL lysozyme tris buffer solution, and let stand at room temperature for 50 minutes , forming a thin film on the surface of the mixed solution, that is, a two-dimensional nano-film of biological protein, with a thickness of about 60nm.
Embodiment 3
[0029] Add 0.1433g of tris(2-carboxyethyl)phosphine into 10mL of 10mmol / L tris(2-carboxyethyl) buffer solution with a pH value of 7.4, adjust the pH value to 6.0 with NaOH, and prepare 50mmol / L of tris(2-carboxyethyl) Tris buffer solution of phosphine; add 20mg lysozyme to 10mL10mmol / L tris buffer solution with pH value of 7.4, and prepare tris buffer solution of 2mg / mL lysozyme Buffer solution; mix 10mL of 50mmol / L tris(2-carboxyethyl)phosphine tris buffer solution with 10mL 2mg / mL lysozyme tris buffer solution, and let stand at room temperature for 50 minutes , forming a thin film on the surface of the mixed solution, that is, a two-dimensional nano-film of biological protein, with a thickness of about 60nm.
PUM
Property | Measurement | Unit |
---|---|---|
Particle size | aaaaa | aaaaa |
Thickness | aaaaa | aaaaa |
Thickness | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
![application no application](https://static-eureka.patsnap.com/ssr/23.2.0/_nuxt/application.06fe782c.png)
- 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