Human Medical Research Detection Kits

Alta DiagnoTech provides research kits for detecting human medical research diagnostics for genetic research. Our kits in the planning stage include:

At the moment, the human SMN1/DMD/FMR1 mutation detection kit is ready and we offer it as a simple solution for the diagnosis of gene mutations caused by spinal muscular atrophy (SMA), Duchenne muscular dystrophy (DMD), and fragile X syndrome (FXS). Alta DiagnoTech strives to provide effective and high-quality tools for human genetic research.

Our Mutation Detection Kit

The human SMN1/DMD/FMR1 mutation detection kit is the first solution to offer combined screening for spinal muscular atrophy (SMA), Duchenne muscular dystrophy (DMD), and fragile X syndrome (FXS). With PCR and capillary electrophoresis technology, precise results are achieved in under 8 hours. Gene copy numbers, large deletions, and duplications, point mutations in SMN1, SMN2, and DMD genes along with CGG repeats in FMR1 are detected employing the kit.

Human SMN1/DMD/FMR1 Mutation Detection Kit

Our custom kits for the detection of genetic alterations such as mutations, single nucleotide polymorphisms, and their chromosomal locations are aimed at human medical research and offer a multitude of application possibilities, from whole genome amplification to complex mutation detection. Our products and services, enhanced with innovative science and comfortable workflows, will help any researcher looking for reliable means for genetic discoveries. Work with Alta DiagnoTech to enhance your research and diagnostic potential!

These products and services are for research use only and cannot be used for any clinical purposes!