Genetic Disease Research
Genetic diseases are caused by various genome abnormalities and can be inherited from parental genes or, more often, caused by new mutations or alterations in the genetic material of an individual. Some of the more commonly observed genetic modifications include single mutations, deletions, insertions, inversions, copy number changes, and methylation differences. We offer a number of Applied Biosystems® kits and workflow solutions that, when used together with our genetic analyzers, help you get answers to your genetic disease research questions.
Screening Prior to Sequencing
SSCP is an electrophoretic mobility assay used to find variants in a large number of samples so that fewer DNA sequencing runs are needed.
DNA mutations are the most common events driving the development of cancer. Our kits and genetic analysis instruments help simplify your application development process—for example SNP detection (a single SNP or up to 10 SNPs located on different DNA segments) and sequencing complete genes.
Genetic rearrangements—including duplications, inversions, and deletions of DNA fragments—are known to contribute to many genetic diseases.
DNA methylation plays an important role in the regulation of gene expression and, consequently, in the appearance of various disease states. Using our methylation detection solutions, you can determine the overall level of methylation or identify the methylation status of a specific CpG.
New Capillary Electrophoresis Instruments Support Center
Find tips, troubleshooting help, and resources for support related to your capillary electrophoresis instruments.
For Research Use Only. Not for use in diagnostic procedures.