Hereditary Deafness gDNA Reference Products

Current Status of Hereditary Deafness Research

Hereditary deafness is a condition in which a person is born with a hearing loss or becomes deaf over time due to genetic factors. Hereditary deafness can be caused by mutations in a single gene or multiple genes, and the main modes of inheritance include autosomal dominant, autosomal recessive, X-linked and mitochondrial inheritance. There is no cure for hereditary deafness, the assistive devices can be used to help manage symptoms and improve communication for those affected. Genetic counseling and testing is important for individuals and families affected by genetic deafness to help determine the type and cause of the disease and to inform family planning decisions. There are different types of tests for genetic deafness, including targeted tests, genetic panel tests and whole exome sequencing.

CD Genomics offers a wide range of hereditary deafness gDNA standards to assist you in identifying any genetic mutations that may contribute to their hearing loss, providing valuable information about the cause of hearing loss and the risk of passing it on to offspring.

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Hereditary Deafness gDNA Reference Products Details

Our technical team has developed hereditary deafness gDNA reference products can be used throughout the methodological process of deafness mutation detection to help clients monitor and revise their hereditary deafness analysis protocols, standardize their practices, and perform bioinformatics analysis.

Origin

Our hereditary deafness gDNA reference products are derived from human cell lines.

Product Highlights

Maximizes the simulation of clinical samples.
Comprehensive loci, including 4 common deafness-related genes GJB2, GJB3, SLC26A4, and mitochondrial 12S rRNA.
Positive and negative standards can be freely combined according to the desired loci.
PCR and NGS platforms are available.

Applications

Evaluate the efficiency of the hereditary deafness detection process.
Evaluate the impact of background noise on the detection of genetic deafness variants.
Validate the robustness of bioinformatics processes.
Optimize and validate new assay panels and monitor process performance.
Detect detection and quantification limits of hereditary deafness processes.
Analyze the sensitivity, accuracy and specificity of the detection process.
Compare assay differences across platforms, such as fluorescent polymerase chain reaction (PCR), gene chip hybridization, Sanger sequencing, next generation sequencing (NGS), etc.

* For Research Use Only. Not for use in diagnostic procedures.

Explore Our Hereditary Deafness gDNA Reference Products:

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Cat. No.	Product Name	Brief Description
HDGR001	CD Hereditary Deafness GJB2 gDNA Reference	CD Hereditary Deafness GJB2 gDNA Reference is suitable for the whole process of each method, which can help you monitor and correct the experimental protocol, Referenceize the operation and bioinformatics analysis process, etc.
HDGR002	CD Hereditary Deafness GJB3 gDNA Reference	CD Hereditary Deafness GJB3 gDNA Reference is suitable for the whole process of each method, which can help you monitor and correct the experimental protocol, Referenceize the operation and bioinformatics analysis process, etc.
HDGR003	CD Hereditary Deafness SLC26A4 gDNA Reference	CD Hereditary Deafness SLC26A4 gDNA Reference is suitable for the whole process of each method, which can help you monitor and correct the experimental protocol, Referenceize the operation and bioinformatics analysis process, etc.
HDGR004	CD Hereditary Deafness Mitochondrial 12S rRNA gDNA Reference	CD Hereditary Deafness Mitochondrial 12S rRNA gDNA Reference is suitable for the whole process of each method, which can help you monitor and correct the experimental protocol, Referenceize the operation and bioinformatics analysis process, etc.