Detection kit based on Trinder reaction and application of detection kit
A detection kit and reagent technology, applied in the field of clinical chemical detection, can solve the problems of affecting the measurement results, misdiagnosis, and misinterpretation of test results, etc.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0039] Embodiment 1 creatinine detection kit
[0040] This embodiment provides a creatinine detection kit, which is compared with a conventional creatinine detection kit, wherein the detection kit of the present invention is the test group 1, and the conventional creatinine detection kit is the control group 1, and the formula details as follows:
[0041]
[0042] Wherein the test group one compared with the control group one, added 150KU / L of peroxidase and 1g / L of 4-aminoantipyrine in the R1 reagent component to be used for consuming medicine, simultaneously due to peroxidase The stability of catalase is poorer than that of catalase, so test group one also added an appropriate amount of metal ion chelating agent HEDTA and surfactant GENAPOLX-080 in the R1 reagent components to ensure the stability of peroxidase; test Group 1 also added 1g / L DHBS to the R2 reagent component instead of TOOS in the control group 1 R1 reagent component as the chromogen substrate.
[0043] T...
Embodiment 2
[0055] Embodiment 2 free fatty acid detection kit
[0056] This embodiment provides a free fatty acid detection kit, and compared with the conventional free fatty acid detection kit, wherein the detection kit of the present invention is the test group two, and the conventional creatinine detection kit is the control group two, The formula is as follows:
[0057]
[0058]
[0059] Compared with the control group two, the test group two added 100KU / L of peroxidase and 0.5g / L of 4-aminoantipyrine to the R1 reagent components to consume the drug, and there was no Contain metal ion chelating agent and surfactant; Added 1g / L HAOS in the R2 reagent component to replace the TOOS in the control group—R1 reagent component as the chromogen substrate. The determination method was the same as that in Example 1, wherein the volume of each sample was 5 μL, and 240 μL of R1 reagent and 60 μL of R2 reagent were added. Measure the performance of the control group 2 and the test group 2 ...
Embodiment 3
[0072] Example 3 Triglyceride Detection Kit
[0073] This embodiment provides a triglyceride detection kit, and compared with the conventional triglyceride detection kit, wherein the test group three is the detection kit of the present invention, and the control group three is the conventional triglyceride detection kit The specific formula of the detection kit is as follows:
[0074]
[0075] Wherein test group three is compared with control group three, in the R1 reagent component, has added the 4-aminoantipyrine of 4mmol / L (0.81g / L), promptly added peroxidase and simultaneously before Trinder reaction 4-aminoantipyrine, while the control group 3 is 4-aminoantipyrine added to the R2 reagent components for Trinder reaction, while the test group 3 added DHBS to the R2 reagent components to replace the control group The p-chlorophenol in the three R1 reagent components is used as the chromogen substrate. The determination method is as shown in Example 1, wherein the volume...
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