Human Genetics Equipment For Medical Specialties
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Manufactured by Advanced Molecular Diagnosticsbased in UNITED KINGDOM
More than 1,000 mutations in the CFTR gene have been associated with cystic fibrosis. Most of these mutations in the CFTR gene change the production, structure, or stability of the chloride channel. All of these charevent the channel from functioning properly, which impairs the transport of chloride ions and the movement of water into and out of cells, resulting in cells lining the passageways of ...
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based in USA
CGx Testing is a preventative gene test that looks for specific inherited changes (mutations) in a person’s genetic make-up. Harmful mutations may increase a persons’ chance, or risk, of developing a disease such as cancer. These conditions are considered hereditary. Appropriate genetic testing may be used to determine an individual’s risk and potential treatment options as ...
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Manufactured by Elicio Therapeuticsbased in USA
Our lymph node-targeted mKRAS cancer vaccine; Our Amphiphile (AMP)-powered lead candidate, ELI-002, generates a robust immune response against mutant Kristen rat sarcoma (mKRAS), with the potential to offer patients a stronger fight against the most aggressive cancers. Preliminary data have shown that ELI-002 produces a potent mKRAS-specific T-cell response, including both CD4+ and CD8+ ...
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based in USA
Protein misfolding is the root of many diseases, including lysosomal storage disorders and neurodegenerative ...
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Manufactured by Eyevensysbased in FRANCE
EYS611 encodes the human transferrin protein, a natural iron transporter involved in the control of iron levels in the eye. Iron is needed for retinal cell metabolism, but excess free iron causes oxidative stress and is extremely toxic to the retina. Iron overload is associated with a number of degenerative retinal diseases, including AMD, retinitis pigmentosa (RP), and glaucoma. Eyevensys is ...
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Manufactured by Therawisbased in GERMANY
Exosomes (30-150 nm) are the smallest type of extracellular microvesicles (EMV), produced through inward budding multivesicular bodies (MVB), resulting in intra-luminal vesicles (ILV). ILVs are released into the extracellular media by exocytosis. Exosome-associated proteins are used to isolated microvesicles from biological fluids such as blood, urine or cerebral fluid and to identify the source ...
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Manufactured by Genetic Signatures Ltd.based in AUSTRALIA
The EasyScreen™ Essentials Respiratory Detection Kit enables multiplex real-time PCR testing for leading viral pathogens that cause respiratory tract infections, including SARS-CoV-2. A full list of the essential respiratory pathogen targets is listed in the table below. User friendly medium to high-throughput systems are available that support Genetic Signatures’ full range of unique ...
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Manufactured by Scopus BioPharmabased in USA
Our licensed gene therapy, CO-sTiRNA™, is a dual-action STAT3 inhibitor. STAT3 is a gene that drives tumor cell growth and anti-tumor immune suppression. CO-sTiRNA™ is a highly selective and targeted gene therapy that silences the activity of the STAT3 gene by way of RNA interference. CO-sTiRNA™ also stimulates TLR9 receptors to activate the body’s immune defense to ...
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Manufactured by TIB Molbiol Syntheselabor GmbHbased in GERMANY
In 2005 we developed our first LightMix Kit detecting bird flu Influenza A H5N1. Since then, we have created many kits testing for different pathogens, hematology markers, genetic mutations and polymorphisms. ...
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based in USA
Genome editing is efficient, precise and scalable. CRISPR/Cas9 genome editing can make permanent, precisely targeted changes in patients’ chromosomes and repair the underlying genetic mutation, whereas more traditional gene therapy typically involves introducing a non-permanent copy of a gene into patients’ cells. These attributes of CRISPR/Cas9 provide a significant therapeutic edge ...
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Manufactured by KORU Medical Systemsbased in USA
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare, chronic, life-threatening blood disorder characterized by the complement-mediated destruction (hemolysis) of oxygen-carrying red blood cells. The disease is caused by a genetic mutation in the DNA and causes red blood cells to be missing a critical protein responsible for protecting them. Hemolysis occurs in PNH through two mechanisms: ...
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based in USA
Human diseases are mainly caused by problems in regulation and functioning of internal body parts due to genetic impact or problems caused during their lifetime. There are many complex biological processes occurring in the body cells and there are many interactions between proteins and other elements carried out as molecular interactions. Molecular medication mechanisms have been introduced into ...
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Manufactured by MedGenome Inc.based in USA
OncoPeptTUME — A novel in-silico approach to model the tumor microenvironment and predict treatment efficacy and long-term survival benefits for immunotherapy applications. Cancer immunotherapy is now established as a major therapeutic modality. Cancer immunotherapy drugs elicit their anti-tumor immune response in a subset of the treated patients by activating CD8 T-cells and provide ...
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Manufactured by Pharmaxis Ltdbased in AUSTRALIA
Cystic fibrosis (CF) is an inherited, life-limiting disease that affects the body's exocrine glands, which produce mucus, saliva, sweat and ...
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