Profile: Theratest Laboratories manufactures & distributes elisa-based diagnostic test kits for the detection and measurement of autoantibodies for rheumatic diseases. We offer products like anticular antibodies, antiophospolipid syndrome, rheumatoid arthritis, celiac disease, bone & mineral metabolism, quality control & proficiency testing, test processing system, haematology & chemistry analyzer, laboratory information system & urine analyzer. Our anticardiolipin antibody test kit is a single test kit that contains everything necessary to perform any combination of polyvalent screening or isotype-specific measurement (IgM, IgG and IgA) of aCL antibodies. Our EL-ANA/6 elisa tests are used for the detection and measurement of panels of autoantibodies.
The company was founded in 1988, has revenues of USD 1-5 Million and is ISO certified.
FDA Registration Number: 1421346
17 Products/Services (Click for related suppliers)
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• Anti-MPO ANCA |
• Anti-MPO ANCA EIA Auto-Immune Markers Testing Kit |
• Anti-PR3 ANCA |
• Anti-Ribosomal P Antibodies (FDA Code: MQA / 866.5100) An antinuclear antibody immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the autoimmune antibodies in serum, other body fluids, and tissues that react with cellular nuclear constituents (molecules present in the nucleus of a cell, such as ribonucleic acid, deoxyribonucleic acid, or nuclear proteins). The measurements aid in the diagnosis of systemic lupus erythematosus (a multisystem autoimmune disease in which antibodies attack the victim's own tissues), hepatitis (a liver disease), rheumatoid arthritis, Sjogren's syndrome (arthritis with inflammation of the eye, eyelid, and salivary glands), and systemic sclerosis (chronic hardening and shrinking of many body tissues). |
• Anti-RNP Antibody (FDA Code: LKO / 866.5100) |
• Anti-SM-Antibody (FDA Code: LKP / 866.5100) |
• Antigen And Control Extractable Antinuclear Antibody (FDA Code: LLL / 866.5100) |
• Antineutrophil Cytoplasmic Antibodies (ANCA) Test System (FDA Code: MOB / 866.5660) A multiple autoantibodies immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the autoantibodies (antibodies produced against the body's own tissues) in serum and other body fluids. Measurement of multiple autoantibodies aids in the diagnosis of autoimmune disorders (disease produced when the body's own tissues are injured by autoantibodies). |
• B2 - Glycoprotein I Antibodies Test System (FDA Code: MSV / 866.5660) |
• Endomysial Autoantibodies (FDA Code: MVM / 866.5660) |
• Enzyme Labeled Anti-DNA Antibody (FDA Code: LRM / 866.5100) |
• Enzyme Labeled Antinuclear Antibody (FDA Code: LJM / 866.5100) |
• Gliadin Antibodies (FDA Code: MST / 866.5750) A radioallergosorbent immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the allergen antibodies (antibodies which cause an allergic reaction) specific for a given allergen. Measurement of specific allergen antibodies may aid in the diagnosis of asthma, allergies, and other pulmonary disorders. |
• Immunological Anticardiolipin Test System (FDA Code: MID / 866.5660) |
• Rheumatoid Factor Test System (FDA Code: DHR / 866.5775) A rheumatoid factor immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the rheumatoid factor (antibodies to immunoglobulins) in serum, other body fluids, and tissues. Measurement of rheumatoid factor may aid in the diagnosis of rheumatoid arthritis. |
• Thyroid Autoantibody Test System (FDA Code: JZO / 866.5870) A thyroid autoantibody immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the thyroid autoantibodies (antibodies produced against the body's own tissues). Measurement of thyroid autoantibodies may aid in the diagnosis of certain thyroid disorders, such as Hashimoto's disease (chronic lymphocytic thyroiditis), nontoxic goiter (enlargement of thyroid gland), Grave's disease (enlargement of the thyroid gland with protrusion of the eyeballs), and cancer of the thyroid. |
• Whole Human Serum (FDA Code: DGR / 866.5700) A whole human plasma or serum immunological test system is a device that consists of reagents used to measure by immunochemical techniques the proteins in plasma or serum. Measurements of proteins in plasma or serum aid in the diagnosis of any disease concerned with abnormal levels of plasma or serum proteins, e.g., agammaglobulinemia, allergies, multiple myeloma, rheumatoid vasculitis, or hereditary angioneurotic edema. |