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Genetic Disease Services
17 services found
Manufactured by:Creative Biolabs based inShirley, NEW YORK (USA)
Creative Biolabs provides a comprehensive range of primary antibodies for genetic disorders. These antibodies show high specificity, activity, performance and repeatability in a variety of technologies, including: ...
Manufactured by:Creative Biolabs based inShirley, NEW YORK (USA)
Genes are the basis of heredity. Sometimes, one or more genes mutated and changed can lead to a medical condition called a genetic disease. Antibodies to genetic diseases bind to proteins involved in genetic diseases and have a wide range of uses in basic research. ...
Manufactured by:CENTOGENE N.V. based inRostock, GERMANY
Carrier screening can determine if a healthy person carries a genetic disease, identify people at risk of developing a genetic disease, or help assess the risk of a couple passing a genetic disease onto their children. ...
by:Lovelace Biomedical based in, DISTRICT OF COLUMBIA (USA)
Lovelace Biomedical is very much focused on gene therapy for genetic diseases testing in human clinical trials. Our ultimate aim is to give best gene therapy medicine. http://www.lovelacebiomedical.org/specialty-expertise/gene-therapy/ ...
Manufactured by:Ozgene Pty Ltd. based inBentley DC, AUSTRALIA
Knockout mice are animal models that have been genetically modified to delete or inactivate a specific gene. The term ‘knockout’ refers to knocking out the functionality of the target gene. These mouse models allow researchers to gain insight into how the loss of the gene affects physiology, behavior and disease development. Observing the ...
Manufactured by:CENTOGENE N.V. based inRostock, GERMANY
The fastest and most comprehensive genetic testing available for newborns, infants and children less than 24 months old in intensive care. CentoICU – Genetic Testing When Every Moment Counts. Up to one-third of all babies and children admitted to the ICU have a genetic disease. ...
Manufactured by:Deep Genomics based inToronto, ONTARIO (CANADA)
AI Drives Unprecedented Number of Valuable Medicines by Combining Prediction and Scale. Our proprietary AI Workbench is designed for data-driven prediction, positive feedback loops, and exponential growth. It enables us to identify leads for over 50% of the novel targets we select, and to do so quickly. This is a game changer. In 2018, our proprietary AI Workbench unlocked our first targets in ...
by:Admera Health based inSouth Plainfield, NEW JERSEY (USA)
Most disease-related variants are found in exons, exome sequencing is a method to understand genetic causes of diseases or conditions. Optimized workflow for FFPE samples. Expert scientific and project support. IDT, SureSelect, Twist Biosciences, Illumina capture options. ...
by:National Institute of Environmental Health Sciences (NIEHS) based inResearch Triangle Park, NORTH CAROLINA (USA)
As an institute, the NIEHS is uniquely positioned to investigate the interplay between environmental exposures, human biology, genetics, and common diseases that limit our longevity and quality of life. NIEHS research uses state-of-the-art science and technology to understand how environmental factors influence the development and progression of ...
Manufactured by:CENTOGENE N.V. based inRostock, GERMANY
Whole genome sequencing (WGS) identifies almost all changes in a patient’s DNA by sequencing both the entire protein coding and the non-coding regions of the ...
Manufactured by:BioMarin based inSan Rafael, CALIFORNIA (USA)
In alignment with our commitment to scientific innovation and areas of unmet medical need, we may provide product and funding support for independent research in rare diseases and genetic ...
Manufactured by:BioMarin based inSan Rafael, CALIFORNIA (USA)
In alignment with our commitment to scientific innovation and areas of unmet medical need, we may provide product and funding support for independent research in rare diseases and genetic ...
Manufactured by:CENTOGENE N.V. based inRostock, GERMANY
Whole Exome Sequencing (WES) is a comprehensive genetic test that identifies changes in a patient's DNA that are causative or related to their medical concerns. By focusing on the entire protein-coding regions of the genome – the exome – WES offers you the coverage you need to diagnose patients rapidly and ...
Manufactured by:RareStone Group based inShanghai, CHINA
Rare neurological diseases include developmental defects of the nervous system, genetic and metabolic diseases, neuroimmune diseases, neurological tumors, special types of infectious diseases of the nervous system, neurodegenerative diseases, and neuromuscular diseases. At ...
Manufactured by:CENTOGENE N.V. based inRostock, GERMANY
Genetic testing is a type of medical test that identifies changes in genes, inherited from our parents, which we then typically pass on to our children. “Mistakes” in our genes (called “pathogenic variants”) can manifest the disease, and genetic tests may be used to confirm the disease ...
by:Avero Diagnostics based inIrving, TEXAS (USA)
Expectant parents want to do everything they can before the birth of their baby. The Avero Carrier Test looks at a patient’s genes to see if they may carry a disease that they could pass on to their child. Knowing a patient’s genetic carrier status is one of the most important things you can do to help them prepare for ...
by:MtoZ Biolabs based in, MASSACHUSETTS (USA)
Different fatty acids (FAs) vary greatly in the number of double bonds and the length of their carbon (C) chains. Very long-chain fatty acids (VLCFAs) are fatty acids with more than 20 carbon atoms. VLCFAs are precursors of lipid mediators and are components of cellular lipids such as sphingolipids and glycerophospholipids. ...