Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Multiple PCR detection kit for 11 intestinal pathogen nucleic acid and application of detection kit

A technology for detection kits and pathogenic bacteria, which is applied in the determination/testing of microorganisms, resistance to vector-borne diseases, microorganisms, etc., can solve problems such as interactions, and achieve high detection sensitivity, guaranteed reliability, and good specificity Effect

Active Publication Date: 2016-04-27
NANJING MOKOBIO BIOTECH +2
View PDF3 Cites 16 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0013] The technical problem solved by the present invention: In order to solve the problem of interaction between multiple pairs of primers in the same reaction system, the present invention adopts the multiplex PCR amplification technology of general primers

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Multiple PCR detection kit for 11 intestinal pathogen nucleic acid and application of detection kit
  • Multiple PCR detection kit for 11 intestinal pathogen nucleic acid and application of detection kit
  • Multiple PCR detection kit for 11 intestinal pathogen nucleic acid and application of detection kit

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 111

[0049] Embodiment 111 kinds of intestinal pathogenic bacteria nucleic acid multiplex PCR detection kit

[0050] The kit consists of primer mix A, primer mix B, PCR reaction buffer, enzyme system, positive control, negative control and DEPC water.

[0051] PCR reaction solution A is a mixture of primer mixture A and PCR reaction buffer; PCR reaction solution B is a mixture of primer mixture B and PCR reaction buffer.

Embodiment 2

[0052] Operation and result determination of embodiment 2 kit

[0053] (1) Extraction of bacterial genomic DNA

[0054] Pick the feces the size of rice grains (take the mucus, pus and blood as much as possible), put them in a centrifuge tube with 0.5ml of normal saline, shake and mix well, and centrifuge at 13,000rpm for 2min, remove the supernatant, and precipitate for later use. Use the fecal nucleic acid extraction kit (product number: DP328) from Tiangen Biochemical Technology Co., Ltd. to extract nucleic acid in the sample processing area according to the instructions.

[0055] (2) Preparation of amplification system

[0056] The following experiments were carried out using the kit of Example 1. After the components of the kit were completely dissolved at room temperature, they were quickly shaken and mixed. 25 μL PCR amplification system A reaction system is: 18 μL each of PCR reaction solution A, 2 μL enzyme system, 2-5 μL template (including nucleic acid extracted fr...

Embodiment 3

[0065] Embodiment 3 kit specific experiment

[0066] Select 8 enterovirus samples including coxsackievirus, poliovirus, echovirus, enteroadenovirus, norovirus, astrovirus, rotavirus group A, and zaravirus, as well as campylobacter jejuni and mononuclear virus 4 kinds of intestinal bacteria of cell proliferative Listeria, Vibrio alginolyticus, and Aeromonas, using the kit described in Example 1 to operate and determine the results according to the method described in Example 2, the detection results of the above 12 pathogens No characteristic peaks with peak sizes shown in Table 2 were shown, indicating that the kit of the present invention has good specificity.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention discloses a multiple PCR detection kit for 11 intestinal pathogen nucleic acid and application of the detection kit. The detection kit comprises primers for amplifying 11 intestinal pathogens which include vibrio cholerae serotype O1, vibrio cholerae serotype O139, salmonella, Shigella, vibrio parahaemolyticus, Yersinia enterocolitica, enterophathogenic escherichia coli (EPEC), enteroinvasive escherichia coli (EIEC), enteroaggregative escherichia coli (EAEC), enterotoxigenic escherichia coli (ETEC) and escherichia coli O157:H7. The multiple PCR detection kit has the advantages that the kit is capable of performing multiple detection, high in sensitivity and fast and convenient to use; specific primer sequences are used to guarantee detecting result reliability; the detection method is simple to operate, time saving, labor saving, high in detection throughput, low in reagent consumable cost, capable of directly detecting the nucleic acid extracted from encephalitis pathogens, low in detection platform and staff technical level requirements and capable of being widely popularized in conventional detection.

Description

technical field [0001] The invention belongs to the field of gene detection, and relates to a kit for detecting nucleic acids of 11 kinds of intestinal pathogenic bacteria by using a multiplex PCR amplification method mediated by universal primers and an application thereof. Background technique [0002] Diarrhea is a common and frequently-occurring disease in summer and autumn, with serious harm, complex causes, and a wide range of susceptible populations. The main pathogens include bacteria, viruses, and biological factors, and bacterial infection is the most common cause of diarrhea. In addition, the national food safety standard (GB29921-2013) stipulates the limit requirements for pathogenic bacteria in food. Therefore, intestinal pathogenic bacteria are important detection items for clinical diagnosis and food safety inspection. [0003] Enteropathogenic bacteria mainly include diarrhea-causing Escherichia coli, Vibrio cholerae, Salmonella, Shigella, Yersinia enterocol...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): C12Q1/68C12Q1/10C12Q1/04C12R1/63C12R1/42C12R1/19C12R1/01
CPCC12Q1/686C12Q1/689C12Q2600/16C12Q2537/143C12Q2565/125Y02A50/30
Inventor 刘文干谢国祥金鑫丁洁朱坤张平
Owner NANJING MOKOBIO BIOTECH
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

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