Preparation of kit and method for rapidly detecting carotene components in foods and beverages
A technology for detecting kits and carrots, which is applied in biochemical equipment and methods, material stimulation analysis, microbe determination/inspection, etc., and can solve problems such as discrepancies between product real attributes and labels, inability to identify, and reduction of raw material consumption
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0038] Make the real-time fluorescent PCR detection kit of carrot ingredient by following formula, and reagent wherein comprises as follows:
[0039] (1) PCR amplification reaction solution A
[0040] Including 10×PCR reaction buffer, 0.2mmol / L dNTP (including dUTP), 2mmol / L magnesium sulfate, 0.4μmol / L upstream primer 5′-CGACAAGCAAGCTTTACTCCAA-3′, 0.4μmol / L downstream primer 5′-CGTCTGACACCCATGAGTCTGT-3 ', 0.4 μmol / L Taqman-MGB probe 5'-FAM-TCAAAACAGCCTTGAAAAACCCCACCA-TRAMA-3';
[0041] Wherein 10×PCR reaction buffer contains 100mmol / L tris-hydrochloric acid of pH8.8, 500mmol / L potassium chloride and 1% Triton X-100;
[0042] The mass ratio of the mixture of four deoxyribonucleic acids in the dNTP is dUTP:dATP:dGTP:dCTP=2:1:1:1.
[0043] (2) UNG enzyme: 1U / μL;
[0044] (3) Taq enzyme: 5 U / μL.
[0045] Follow the procedure below for testing:
[0046] (1) Extraction of DNA from carrot noodle samples to be tested
[0047] A. Weigh 0.1g of carrot noodles, cut into pieces, an...
Embodiment 2
[0065] Make the real-time fluorescent PCR detection kit of carrot ingredient by following formula, and reagent wherein comprises as follows:
[0066] (1) PCR amplification reaction solution A
[0067] Including 10×PCR reaction buffer, 0.2mmol / L dNTP (including dUTP), 2mmol / L magnesium sulfate, 0.4μmol / L upstream primer 5′-CGACAAGCAAGCTTTACTCCAA-3′, 0.4μmol / L downstream primer 5′-CGTCTGACACCCATGAGTCTGT-3 ', 0.4 μmol / L Taqman-MGB probe 5'-FAM-TCAAAACAGCCTTGAAAAACCCCACCA-TRAMA-3';
[0068] Wherein 10×PCR reaction buffer contains 100mmol / L tris-hydrochloric acid of pH8.8, 500mmol / L potassium chloride and 1% Triton X-100;
[0069] The mass ratio of the mixture of four deoxyribonucleic acids in the dNTP is dUTP:dATP:dGTP:dCTP=2:1:1:1.
[0070] (2) UNG enzyme: 1U / μL;
[0071] (3) Taq enzyme: 5 U / μL.
[0072] Follow the procedure below for testing:
[0073] (1) Extraction of the DNA of the tomato rice flour sample to be tested
[0074] A. Weigh 0.1g of tomato rice flour and tran...
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