Immco Diagnostics

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Contact: Raul Saona - Director International Sales
Web: http://www.immcodiagnostics.com
E-Mail:
Address: 60 Pineview Drive, Buffalo, New York 14228, USA
Phone: +1-(716)-691-0091 | Fax: +1-(716)-691-0466 | Map/Directions >>

Profile: Immco Diagnostics focuses in the field of autoimmune diagnostics services. We offer products like immuno-fluorescence assays, enzyme linked immuno-sorbent assays, western blot, hearing loss, cardio vascular disorder, neuro-immunological disorder, endocrine disorder, liver disorder & gastrointestinal disorders. Autoimmunity may affect many varied systems in the body. A number of hepatic diseases are autoimmune in nature, including autoimmune hepatitis and pernicious anemia. Prompt and accurate diagnosis of these conditions is essential. Laboratory diagnostics are available to support diagnosis. We manufacture quality assays. Our assays aid in the diagnosis of diverse autoimmune diseases. We also market diagnostic devices. Our kits are available for in vitro diagnostic use and are CE marked.

The company is ISO 9001 certified.

FDA Registration Number: 3003212362
US Agent: Kevin J Lawson / Immco Diagnostics, Inc.
Phone: +1-(716)-691-0091 Fax: +1-(716)-691-0466 E-Mail:

34 Products/Services (Click for related suppliers)

• ANA (Antinuclear antibodies)

• Anti IgG FITC (FDA Code: DGK / 866.5510)

An immunoglobulins A, G, M, D, and E immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the immunoglobulins A, G, M, D, an E (serum antibodies) in serum. Measurement of these immunoglobulins aids in the diagnosis of abnormal protein metabolism and the body's lack of ability to resist infectious agents.

• Anti- Endomysial Antibody (EMA)

• Anti-Endomysial Antibody (EMA) Test System

• Anti-Gliadin (Ab)

• Anti-Gliadin (Ab) IgA Kit

• Anti-Gliadin (Ab) IgG Kit

• Anti-MPO ANCA

• Anti-MPO ANCA EIA Auto-Immune Markers Testing Kit

• Anti-Nuclear Antibody (ANA)ELISA Screen

• Anti-PR3 ANCA

• Anti-RNP Antibody (FDA Code: LKO / 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).

• Antigen and Control Anti-DNA Antibody (FDA Code: LSW / 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).

• Antinuclear Antibody, Indirect Immunofluorescen (FDA Code: DHN / 866.5100)

• Azan Counterstain (FDA Code: ICT / 864.1850)

Dye and chemical solution stains for medical purposes are mixtures of synthetic or natural dyes or nondye chemicals in solutions used in staining cells and tissues for diagnostic histopathology, cytopathology, or hematology.

• B2 - Glycoprotein I Antibodies Test System (FDA Code: MSV / 866.5660)

• Control Antigen Antinuclear Antibody (FDA Code: LKJ / 866.5100)

• Endomysial Antibody

• Endomysial Autoantibodies (FDA Code: MVM / 866.5660)

• Enzyme Immunoassay Test

• 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)

• Indirect Immunofluorescent Multiple Auto Antibody (FDA Code: DBL / 866.5660)

• Indirect Immunofluorescent Test, Antiparietal Antibody (FDA Code: DBJ / 866.5110)

An antiparietal antibody immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the specific antibody for gastric parietal cells in serum and other body fluids. Gastric parietal cells are those cells located in the stomach that produce a protein that enables vitamin B12to be absorbed by the body. The measurements aid in the diagnosis of vitamin B12deficiency (or pernicious anemia), atrophic gastritis (inflammation of the stomach), and autoimmune connective tissue diseases (diseases resulting when the body produces antibodies against its own tissues).

• Ouchterlony Agar Plate Test (FDA Code: JZP / 866.4600)

An ouchterlony agar plate for clinical use is a device containing an agar gel used to examine antigen-antibody reactions. In immunodiffusion, antibodies and antigens migrate toward each other through gel which originally contained neither of these reagents. As the reagents come in contact with each other, they combine to form a precipitate that is trapped in the gel matrix and is immobilized.

• 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.

• Saccharomyces Cerevisiae (S.Cerevisiae) Antibodies (FDA Code: NBT / 866.5785)

The Anti-Saccharomyces cerevisiae (S. cerevisiae ) antibody (ASCA) test system is an in vitro diagnostic device that consists of the reagents used to measure, by immunochemical techniques, antibodies toS. cerevisiae (baker's or brewer's yeast) in human serum or plasma. Detection ofS. cerevisiae antibodies may aid in the diagnosis of Crohn's disease.

• 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.

• Tissue Transglutaminase (tTG) Autoantibody

• Water Soluble Mounting Media (FDA Code: KEQ / 864.4010)

• 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.