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Lateral flow test strip detection kit for detection of bovine-derived components in foods and feeds and application of kit

A test strip and feed technology, which is applied in the fields of molecular biology and immunology, can solve the problems of increasing the complexity of the detection process and losing the convenience of the test strip method, and achieves the effects of easy promotion, high specificity and accurate results.

Inactive Publication Date: 2014-05-07
ANIMAL & PLANT & FOOD INSPECTION CENT OF TIANJIN ENTRY EXIT INSPECTION & QUARANTINE BUREAU
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In terms of primer optimization, the invention patent with the publication number CN 102146432 A - "A method for reducing the dimer of a pair of partially homogeneous primers" describes a primer design method with a short palindromic sequence at the 5' end of the primer, The primer self-cyclizes at room temperature to avoid the formation of heterodimers. The invention patent with the publication number CN 102719547 A - "Reagent for Real-time Fluorescent Quantitative PCR for Detecting HER2 Gene Expression Level" also uses a similar method for real-time quantitative PCR Amplification; Publication No. CN 101842494 A invention patent - "use chimeric primers to reduce heterodimer formation" describes a method of using chimeric primers to amplify; in the optimization of the reaction substrate, The invention patent of publication number CN 101171343A "Containing 3' modified oligonucleotides of pseudo-isocytosine nucleic acid base derivatives and their application as primers or probes" provides a method using specially modified nucleotides as substrates In order to reduce the formation of primer-dimers, the use of probes or the introduction of internal control probes can also reduce the interference of non-specific amplification. The publication number is the invention patent of CN 101957373 A-"a semi-quantitative method of adding internal control nucleic acid to pathogenic nucleic acid "Detection method" is to use internal control probes to reduce interference. Among the above methods, the use of hot start technology and circular primers is a common method, and the rest of the methods either use specially synthesized substrates and substrates, or need to introduce The second hybridization process will increase the complexity of the detection process, especially the probe hybridization method, which loses the convenience of the test strip method due to the need for an incubation process

Method used

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  • Lateral flow test strip detection kit for detection of bovine-derived components in foods and feeds and application of kit
  • Lateral flow test strip detection kit for detection of bovine-derived components in foods and feeds and application of kit
  • Lateral flow test strip detection kit for detection of bovine-derived components in foods and feeds and application of kit

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Experimental program
Comparison scheme
Effect test

Embodiment 1

[0051] 1 Materials and methods

[0052] bovine genomic DNA

[0053] 1.2 Primer design

[0054] 1.3 PCR amplification system:

[0055] 1.3 PCR amplification system:

[0056] Template DNA: bovine genomic DNA 1.0 μl Primer F / R 0.8 μl dNTP 2.0 μl 10X PCR buffer 2.0 μl HS Taq DNA polymerase 0.2 μl ddH2O 13.2 μl total capacity 20 μl

[0057] Reaction conditions:

[0058] 95 ℃ 5 minutes 94 ℃ 30 seconds 55 ℃ 30 seconds 72 ℃ 30 seconds 72 ℃ 5 minutes 30 cycles in total

[0059] At the same time, take 3μl for nucleic acid test strip detection. Take 3μL of the amplification product, add it to 97μL of developing solution for detection and spot on the sample pad, and observe the result after 5 minutes.

[0060] 1.4 PCR specificity experiment

[0061] Use the established PCR reaction system for 1: mouse; 2: cow; 3: rabbit; 4: horse; 5: sheep; 6: dog; 7: pig; 8: cat; 9: chicken; 10:...

Embodiment 2

[0068] The sensitivity of the nucleic acid test strip detection method, the PCR template is 1 / 10, 1 / 10 2 , 1 / 10 3 , 1 / 10 4 , 1 / 10 5 , 1 / 10 6 , 1 / 10 7 , 1 / 10 8 , 1 / 10 9 , 1 / 10 10 After dilution, the PCR system was established for amplification.

[0069] 1 Materials and methods

[0070] bovine mitochondrial DNA

[0071] 1.2 Primer design

[0072]1.3 PCR amplification system:

[0073] Template DNA: plasmid DNA 10 μl upstream primer 0.8 μl downstream primer 0.8 μl dNTP 2.0 μl 10X PCR buffer 2.0 μl HS Taq DNA polymerase 0.2 μl wxya 2 o 4.2 μl total capacity 20 μl

[0074] Reaction conditions:

[0075] 95 ℃ 5 minutes 94 ℃ 30 seconds 56 ℃ 30 seconds 72 ℃ 30 seconds 72 ℃ 5 minutes 30 cycles in total

[0076] Take 5 μl for agarose gel electrophoresis. The gel electrophoresis conditions are: 1X TBE buffer, voltage 100V, electrophoresis time 30 minutes. At the s...

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Abstract

The invention discloses a preparation method and an application method of a nucleic acid rapid detection kit for Bostaurus components in feeds and belongs to the field of molecular biology and immunology. According to the preparation method and the application method, a high-sensitivity and high-specificity method of a polymerase chain reaction in nucleic acid detection is combined with an immuno gold staining rapid detection technology in immunology detection; a unique primer is designed and the primer is labeled; an extracted target DNA is subjected to specific amplification and an amplified product is combined with a labeled antibody immobilized on a test strip in a developing solution to form a stable and visible detection strip and a quality control strip, so as to realize rapid and accurate detection on the bovine-derived components in food and feed.

Description

technical field [0001] The invention belongs to the field of molecular biology and immunology, and relates to the PCR nucleic acid amplification of bovine DNA in food and feed and the preparation and application method of a lateral flow immune colloidal gold test strip kit. Background technique [0002] In order to prevent the spread of bovine spongiform encephalopathy (BSE) through beef and beef bones added to animal feed, the European Union and the United States in 1994 and 1997 respectively enacted a ban on adding ruminants to ruminant feed Regulations for protein of animal origin, the European Union in 2000 extended this ban to prohibit feeding processed mammalian, bird and fish protein ingredients to animals intended for food. The "Administrative Measures for the Safety and Hygiene of Animal-derived Feed Products" promulgated by the Ministry of Agriculture of my country in 2004 stipulates that the use of animal-derived feed products (except milk and dairy products) in r...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12Q1/68
CPCC12Q1/6804C12Q2531/113C12Q2563/131C12Q2565/625
Inventor 郑文杰贺艳陈其勇程瑜张宏伟张灿奚文辉杜敬韩宇宁尹长城刘斯奇李宏虹张亚莲
Owner ANIMAL & PLANT & FOOD INSPECTION CENT OF TIANJIN ENTRY EXIT INSPECTION & QUARANTINE BUREAU
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