Preparation method for detecting biotoxicity of nodularin
A biotoxic, nodular algae technology, applied in biochemical equipment and methods, microbial determination/inspection, testing of organic pollutants in water, etc., can solve the problems of low sensitivity, rough results, large consumption of toxins, etc. The effect of good reproducibility, few influencing factors, and simple mortality
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0021] The present invention is applied to the biotoxicity detection of 5 μg / mL nodular toxin (NOD):
[0022] (1) Human umbilical vein endothelial cells were placed at a temperature of 37°C and an air humidity of 95% (containing 5% CO 2 ) in a cell culture box, cultivated in RPMI1640 culture medium containing 20% fetal bovine serum, 60 μg / mL endothelial cell growth supplement and 1% penicillin-streptomycin double antibody.
[0023] (2) Take the cells of passage 3, add phosphate buffer solution (PBS) respectively as blank sample A, add nodularin water sample as test sample B, place on a mixer and shake for 2 hours.
[0024] (3) Wash the cells of samples A and B twice with PBS, and prepare the concentration of about 1×10 5 cells / mL cell suspension;
[0025] (4) Add 5 μL Annexin V-FITC to A and B samples and mix well, then add 5 μL propidium iodide (PI) and mix well; room temperature, dark, reaction 5-15min; within 1 hour, perform flow cytometry Cytometer detection.
[0026...
Embodiment 2
[0031] The present invention is applied to the biotoxicity detection of 10 μg / mL nodular toxin (NOD):
[0032] (1) Human umbilical vein endothelial cells were placed at a temperature of 37°C and an air humidity of 95% (containing 5% CO 2 ) in a cell culture box, cultured in RPMI1640 culture medium containing 10% fetal bovine serum, 60 μg / mL endothelial cell growth supplement and 1% penicillin-streptomycin double antibody.
[0033] (2) Take the cells of passage 3, add phosphate buffer solution (PBS) respectively as blank sample A, add nodularin water sample as test sample B, place on a mixer and shake for 2 hours.
[0034] (3) Wash the cells of samples A and B twice with PBS, and prepare the concentration of about 5×10 5 cells / mL cell suspension,;
[0035] (4) Add 5 μL Annexin V-FITC to A and B samples and mix well, then add 5 μL propidium iodide (PI) and mix well; room temperature, dark, reaction 5-15min; within 1 hour, perform flow cytometry Cytometer detection.
[0036] ...
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