Rapid Detection Kit for Shigella Spp. in Food Nucleic Acid Testing (24 Tests) Thermostatic Fluorescence Method

Product Details
Customization: Available
Specific Usage: For Biological Purpose, For Microbiological
Content: Standard
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  • Rapid Detection Kit for Shigella Spp. in Food Nucleic Acid Testing (24 Tests) Thermostatic Fluorescence Method
  • Rapid Detection Kit for Shigella Spp. in Food Nucleic Acid Testing (24 Tests) Thermostatic Fluorescence Method
  • Rapid Detection Kit for Shigella Spp. in Food Nucleic Acid Testing (24 Tests) Thermostatic Fluorescence Method
  • Rapid Detection Kit for Shigella Spp. in Food Nucleic Acid Testing (24 Tests) Thermostatic Fluorescence Method
  • Rapid Detection Kit for Shigella Spp. in Food Nucleic Acid Testing (24 Tests) Thermostatic Fluorescence Method
  • Rapid Detection Kit for Shigella Spp. in Food Nucleic Acid Testing (24 Tests) Thermostatic Fluorescence Method
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  • Overview
  • Product Description
  • Specification
  • Packing & Delivery
  • Company Profile
  • FAQ
Overview

Basic Info.

Model NO.
KJD06L
Usage
Laboratory Reagents, Analytical Reagents, Diagnostic Reagents, Teaching Reagents
Application
Industry, Scientific Research, Health, Environmental Protection, Agriculture
Sensitivity
Minimum:6 Cfu/Test
Feature
High Efficiency
Customized Support
OEM
Transport Package
Carton
Specification
24 tests/box
Trademark
BHK
Origin
Guangdong, China
HS Code
3821000000

Product Description

Product Description
Introduction
Product introduction: This kit is based on loop-mediated isothermal amplification (LAMP) technology and is used for rapid detection of Shigella in food. The results can be directly interpreted with the help of chromogenic indicators. Principle
Detection principle: Two pairs of special primers and Bst DNA polymerase with strand displacement activity are used to circulate a circular single-stranded structure at the primer junction at both ends of the template. The primers successfully combine with the template and perform strand displacement amplification reaction, achieving constant temperature Continuous and rapid amplification is carried out under certain conditions (60-65°C). When a color indicator is added to the reaction, the color difference between negative and positive results is significant, and the results can be interpreted directly through the color change.
 
Rapid Detection Kit for Shigella Spp. in Food Nucleic Acid Testing (24 Tests) Thermostatic Fluorescence Method
Product features: 1. Quick and easy: Mix the enzyme, primer and other reaction components and then dry them to increase the stability of the reagents. This reduces the steps of solution preparation during use and is more convenient. The entire detection reaction can be completed within 1 hour;
2. High specificity: Multiple primers are designed using multiple independent regions on the target gene sequence to ensure the high specificity of the amplification reaction; 3. High sensitivity: The minimum detection limit reaches 8 CFU/Test;
4. Simple interpretation: Add a color indicator before the reaction, and after the reaction, observe the color change of the reaction solution with the naked eye or track the changes in the fluorescence spectrum through a fluorescence monitoring instrument to interpret the results. This is intuitive and convenient, and can effectively avoid aerosol contamination caused by opening the lid after the reaction
 
Package contains
NO.
 
Product
Specification &Quantity
DRL06
 
Detection reagent (lyophilized)
 3 rows × 8 tubes
FRL01
 
Reconstitution solution
650μL × 1 tube
PRL06
 
Positive control (lyophilized)
1 tube
SHR01
 
Negative control (lyophilized)
1 tube
SHR02
 
Lysis solution
1mL × 1 tube
SHR03
 
Color indicator
80μL × 1 tube
SHR04
 
Ultrapure water
1mL × 1 tube
 
 
Instruction
1 pc
How to use?
1. Sample pretreatment A. Preparation of sample enrichment solution template DNA: a) Pipette 1 mL of enrichment solution into a 1.5 mL sterile centrifuge tube, centrifuge at 6000 r/min for 5 min, discard the supernatant, suspend and wash the precipitate with 50 μL sterile ultrapure water 1-2 times, centrifuge at 6000 r/min for 5 min, and completely remove the supernatant; b) Add 30 μL lysis buffer, fully suspend the bacteria, tap the tube wall to eliminate bubbles, and heat at 99 for 10 min; c) Centrifuge at 12000 r/min for 15 min. The supernatant is the crude DNA, which can be transferred to a 0.2 mL sterile centrifuge tube and can be stored for a long time at -20. B. Preparation of template DNA for suspicious colonies: Pick suspicious colonies, suspend them in a sterile centrifuge tube containing 30 μL lysis buffer, and then follow the above steps b) and c). 2. Reconstitution of negative and positive controls and dry powder reagents A. Reconstitution of negative and positive controls: When used for the first time, add 80 μL of ultrapure water to the positive control and negative control freeze-dried powders, mix well after dissolving, and store at -20 for later use. B. Reconstitution of dry powder reagents: Take out the freeze-dried powder reagents, cut n test reagent tubes as required (n = number of samples to be tested + 1 tube of positive control + 1 tube of negative control), add 20 μL of reconstitution solution to each tube, and dissolve completely for later use. 3. Amplification reaction A. Turn on the instrument that can provide constant temperature conditions and set it to 64 for later use; B. Add 2.5 μL of color indicator to each of the n reaction tubes to which the reconstitution solution has been added; C. Add 2.5 μL of the nucleic acid of the sample to be tested, the negative control, and the positive control to each of the n reaction tubes to which the reconstitution solution has been added, and cover the lids tightly; D. Place all reaction tubes in a constant temperature instrument and react at a constant temperature of 64 for 50 min. 4. Result interpretation: After the reaction is completed, it is recommended to place the sample on a white background under sufficient natural light to observe the results. The negative control test reagent tube is light orange, and the positive control test reagent tube is fluorescent green. The test sample reaction tube is interpreted as a control. If any result of the positive and negative control reaction tubes does not match the above situation, the test result is invalid and should be retested or contact product technical support.
Specification
Our service
1.Offering Sample for Testing .
2.R & D team to provide technical support.
3.Provide packaging, labeling OEM customization.
Packing & Delivery
Rapid Detection Kit for Shigella Spp. in Food Nucleic Acid Testing (24 Tests) Thermostatic Fluorescence Method
Rapid Detection Kit for Shigella Spp. in Food Nucleic Acid Testing (24 Tests) Thermostatic Fluorescence Method
To better ensure the safety of your goods, professional, environmentally friendly, convenient and efficient packaging services will be provided.
Company Profile
 
Guangdong HuanKai Microbial Sci. & Tech. Co.,Ltd. is a national high-tech enterprise under the Guangdong Institute of Microbiology which is attached to Guangdong Academy of Sciences. Since established in 1993, HuanKai has adhered to the strategy of scientific and technological innovation and development, and has formed four product lines including microbiological testing reagents and consumables, digital laboratory instruments, physical and chemical rapid water detecting products, and high-efficiency environmentally friendly cleaning agents and disinfectant, both are with independent intellectual property rights. More than 2, 000 varieties of products are widely applied in mainland China, Hong Kong, Macao, Taiwan and Southeast Asia. Huankai has developed into an important R&D production base for domestic food and other industry.
Rapid Detection Kit for Shigella Spp. in Food Nucleic Acid Testing (24 Tests) Thermostatic Fluorescence Method
Rapid Detection Kit for Shigella Spp. in Food Nucleic Acid Testing (24 Tests) Thermostatic Fluorescence Method
Rapid Detection Kit for Shigella Spp. in Food Nucleic Acid Testing (24 Tests) Thermostatic Fluorescence Method
FAQ
1. Who are we?
HuanKai are based in Guangdong, China, start from 1993,there are total about 301-500 people in HKM. HuanKai has successfully established four major product lines: microbiological testing reagents and consumables, digital laboratory instruments, rapid water testing products for physical and chemical analysis, and eco-friendly cleaning and disinfection solutions. These lines boast over 2,000 different products, each protected by independent intellectual property rights.

2. How can we guarantee quality?
Always a pre-production sample before mass production;
Always final Inspection before shipment;

3.What can you buy from us?
Microbial Detection Product,Peptone&Tryptone,Deydrated Culture Media,Granular Media,Microbial Air Sampler and so on.

4. Why should you buy from us not from other suppliers?
1.With strong R&D capacity and good scientific research conditions,over 30 years of experience 2.One of the largest physicochemical reagent and culture media manufactuer in China follow international standard 3.Stable high quality main raw material from Europe & strictly quality control

5. What services can we provide?
Accepted Payment Currency:USD,EUR,CNY;
Accepted Payment Type: T/T,MoneyGram,PayPal,Western Union,Cash,Escrow;
Language Spoken:English,Chinese

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