Test Environment Notice: This system is a test version; all displayed content is simulated. Test records are cleared periodically. Do not enter real sensitive information.
Global Site
Current template:PCR Kit Template
PCR Test Kit for Detecting Maize-Derived Components
Quantitative Real-Time PCRHigh Sensitivity
PCR DETECTION KIT

PCR Test Kit for Detecting Maize-Derived Components

10 copies
Limit of Detection
40-45
Cyclic number
Get in Touch

Citation Standards

GB/T 27405-2008National Food Safety Standard: Microbiological Examination of Foods — PCR Detection Method
SN/T 1193-2019Nucleic Acid Detection Methods for Foodborne Pathogens in Imported and Exported Foods: Real-Time Fluorescent PCR Method
ISO 22174:2005Microbiology of food and feed — PCR method for detecting genetically modified organisms
Technical Principles

Real-time PCR

Enzymatic reaction based on DNA polymerase that uses real-time fluorescence monitoring of PCR amplification to achieve qualitative or quantitative detection of target nucleic acids.

Nucleic Acid Extraction

Extract target DNA/RNA from samples and remove inhibitors such as proteins and polysaccharides to obtain high-purity nucleic acid templates for PCR.

PCR amplification

Under the guidance of specific primers and fluorescent probes, DNA polymerase catalyzes dNTP incorporation to synthesize a new strand, releasing one fluorescent signal per amplification cycle.

Fluorescence Detection

The instrument acquires fluorescence signals in real time and performs precise quantification of target nucleic acids by comparing Ct values against a standard curve.

Core Performance Metrics

Core Technical Specifications

Rigorous quality control system ensures stability and reliability for every product batch.

Limit of Detection (LOD)
Minimum 10 copies/reaction
Specificity
No cross-reactivity
Linear Range
10^1 - 10^8 copies/mL
Repeatability (CV)
≤3%
Reaction System
25 μL / 50 μL
Packaging Size
48T/box
Amplification Procedure

Standard Amplification Procedure

Optimized reaction conditions to achieve the best balance between amplification efficiency and specificity.

StepsTemperatureTimeCyclic NumberDescription
pre-deformation95°C3-5 min1Activate DNA polymerase
gender transition95°C10-15 sec40-45Collect fluorescence signal
Annealing/Extension55-60°C30-40 sec

Note: Specific reaction conditions may vary depending on the instrument model and target analyte. Please refer to the product manual or consult a technical expert.

Compatible Instruments

Compatible Instruments

Widely compatible with mainstream real-time PCR instruments to meet diverse laboratory equipment needs

ABI 7500 / 7500 Fast
LightCycler 480 II
CFX96 / CFX384
QuantStudio 5 / 6 / 7
Mx3000P / Mx3500P
Rotor-Gene Q

Storage Conditions

Reagent Storage
Store below 20°C in the dark. Valid for 12 months.
Shipping Conditions
Low-temperature cold chain transport to prevent repeated freeze-thaw cycles.
Storage after reconstitution
2-8°C for stable storage of 7 days; long-term storage at -20°C

Important Notes

Not intended for clinical diagnosis.
Wear a lab coat and gloves during operation to prevent contamination.
Vortex all reagents thoroughly and briefly centrifuge prior to use.
Prepare the reaction mixture in a laminar flow hood or biosafety cabinet.
Product Details

Product Details

Nucleic Acid Testing

Downloads & Support

Downloads & Technical Support

A professional technical team providing comprehensive product application and testing solution support.

Need technical consultation?

Our technical expert team will provide you with professional product consulting and customized solutions.

Get Technical Consultation Now