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Side flow test strip detection kit for detecting Gallusgallus ingredients in food and feeding stuff and application of kit

A chicken-derived component and test strip technology, which is applied in the fields of molecular biology and immunology, can solve the problems of losing the convenience of the test strip method and increasing the complexity of the detection process, and achieves easy promotion, high specificity and low cost. Effect

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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  • Side flow test strip detection kit for detecting Gallusgallus ingredients in food and feeding stuff and application of kit
  • Side flow test strip detection kit for detecting Gallusgallus ingredients in food and feeding stuff and application of kit
  • Side flow test strip detection kit for detecting Gallusgallus ingredients in food and feeding stuff and application of kit

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Experimental program
Comparison scheme
Effect test

Embodiment 1

[0051] 1 Materials and methods

[0052] chicken mtDNA

[0053] 1.2 Primer design

[0054] 1.3 PCR amplification system:

[0055] 1.3 PCR amplification system:

[0056] Template DNA: chicken mitochondrial DNA 1.0 μl upstream primer 0.8 μl downstream primer 0.8μl dNTP 2.0 μl 10X PCR buffer 2.0 μl HS Taq DNA polymerase 0.2 μl wxya 2 o 13.2 μl total capacity 20 μl

[0057] Reaction conditions:

[0058] 95 ℃ 5 minutes 94 ℃ 30 seconds 56 ℃ 30 seconds 72 ℃ 30 seconds 72 ℃ 5 minutes 30 cycles in total

[0059] At the same time, take 5 μl for nucleic acid test strip detection, take 5 μL of the amplification product, add it to 95 μL of developing solution for detection and spot on the sample pad, and observe the results 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: ...

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 amplification was carried out according to the established PCR system.

[0069] 1 Materials and methods

[0070] chicken mtDNA

[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 5μl respectively for agarose gel electrophoresis. The gel electrophoresis conditions are: 1X TBE buffer, voltage 100V, electrophoresis t...

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PUM

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Abstract

The invention discloses a preparation method and an application method of a nucleic-acid rapid detection kit for Gallusgallus ingredients in food and feeding stuff, and belongs to the fields of molecular biology and immunology. The detection kit is characterized in that the high-sensitivity and high-specificity method of the polymerase chain reaction in nucleic acid detection is combined with the immune colloidal gold rapid detection technology in immunological detection, unique primers are designed and marked, the extracted target DNA is specifically amplified and the product of the amplification is bonded with gold labeled antibodies immobilized on a test strip in a developing solution, and as a result, stable and visual detection zone and quality control zone are formed, and therefore, rapid and accurate detection on the Gallusgallus ingredients in the food and the feeding stuffing is realized.

Description

technical field [0001] The invention belongs to the field of molecular biology and immunology, and relates to the PCR nucleic acid amplification of chicken-derived components 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 dai...

Claims

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Application Information

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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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