Applications

Birth Defect
Disease Susceptibility
Personalized Medicine
DNA Fingerprinting
Variety Identification
Genetic Quality Assessment

Biochip Development Process

1

Loci confirmation and evaluation
Confirmation of product development content and indicators

2

Complete gene sequence collection, bioinformatics analysis, primer/probe design, primer/probe synthesis, artificial synthesis of gene fragments

3

Complete the screening and optimization of primers and probes, establish and optimize the reagent system, and complete the preliminary finalization of the kit
Interpretation software development, testing

4

Sample testing, verification, optimization, and acceptance check of kit products

Workflow of IMAP

Microfluidic + KASP

Simple: only 1 time sample addition

Flexible: 1 chip can test 1/2/4 samples

Centrifuge and heat-sealing: 2 mins

Physical division of each reaction hole

No cross infection in loci

Amplification: 1.5 h

Scan: 10 mins

Fractal pseudo-color map

Visible QC

One-click output test report

Biochip Design & Fabrication Application Case

Twenty-three Deafness Gene Mutation Detection Kit [Microfluidic Chip Method]

Developed on the IMAP platform, this kit detects 23 mutations across GJB2, SLC26A4, mitochondrial 12S rRNA, and GJB3 using whole-blood or dried-blood-spot samples. The four genes collectively cover more than 90% of the hereditary deafness-associated variants targeted by the assay.

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