Inherited disorder(CE)

CE test kits for Inherited Disorder

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Capillary Electrophoresis (CE)-based genetic testing is a well-established and highly sensitive technique for detecting inherited disorders. By combining fluorescent PCR amplification with capillary electrophoresis, this technology allows for the precise analysis of repeat expansions, copy number variations (CNVs), and other subtle genetic alterations that are difficult to detect using conventional methods. Inherited disorders such as Fragile X Syndrome (FXS) and Spinal Muscular Atrophy (SMA) are often caused by trinucleotide repeat expansions or gene deletions. Accurate and early identification is critical for clinical diagnosis, reproductive decision-making, and long-term patient management. CE-based assays offer high specificity, reproducibility, and resolution, making them ideal for both routine diagnostics and advanced genetic screening.

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High-Resolution Genotyping for Complex Inherited Disorder

Leverage the power of fluorescent PCR and capillary electrophoresis to achieve precise detection of trinucleotide repeat expansions and gene copy number variations. Ideal for diagnosing Fragile X Syndrome, SMA, and other genetically complex conditions with unmatched sensitivity and accuracy.

Streamlined Workflow, Faster Results

From DNA extraction to result interpretation in as little as 4–6 hours. Our CE test kits are optimized for high-throughput laboratories, offering automated compatibility and standardized protocols to enhance efficiency without compromising diagnostic reliability.

Workflow

Inherited Disorder workflow using capillary electrophoresis

* For research purposes only, not intended for clinical diagnosis, treatment, or individual health assessments.

Explore Our Inherited disorder(CE):

Cat. No.	Product Name	Brief Description
PCG001	CDCep™ FMR1 CGG repeat test Kit	Detect Fragile X Syndrome with the CDCep™ FMR1 CGG Repeat Test Kit. Achieve precise CGG repeat analysis for study. Learn more today.
PCG002	CDCep™ SMN Exon Deletion test Kit	Identify SMA with the CDCep™ SMN Exon Deletion Test Kit. Detect SMN1/SMN2 copy numbers with precision for carrier screening & research. Learn more today.
PCG003	CDCep™ Hereditary Deafness Gene test Kit	Screen 21 key mutations with the CDCep™ Hereditary Deafness Gene Test Kit. Enable accurate genetic testing for hearing loss. Learn more today.

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