Profile: Antibodies, Inc. is a supplier of secondary, custom polyclonal and monoclonal antibodies, immunochemistry products & services. We specialize in animal care, antiserum production, immunochemistry and related services applicable to aid the academic or industry research scientist. Peptides can be produced for use as antigens, for conjugation, or as ligands for immunoaffinity purification. We synthesize and conjugate peptides for polyclonal and monoclonal antibody production. Our polyclonal antibodies include antisera, purified antibodies and affinity purified polyclonal antibodies.
The company has revenues of USD 1-5 Million, has ~20 employees and is ISO 9001 certified.
FDA Registration Number: 2914537
41 Products/Services (Click for related suppliers)
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• Albumin Antigen Antiserum Control (FDA Code: DCF / 866.5040) An albumin immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the albumin (a plasma protein) in serum and other body fluids. Measurement of albumin aids in the diagnosis of kidney and intestinal diseases. |
• Albumin, FITC Conjugate (FDA Code: DDZ / 866.5040) |
• Anti IgE FITC (FDA Code: DGP / 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 IgG FITC (FDA Code: DGK / 866.5510) |
• Anti Nuclear Antibody Test Kits |
• Anti-acetylcholine Receptor Alpha Monoclonal Antibody |
• Anti-IgM FITC-Conjugated (FDA Code: DFS / 866.5550) An immunoglobulin (light chain specific) immunological test system is a device that consists of the reagents used to measure by immunochemical techniques both kappa and lambda types of light chain portions of immunoglobulin molecules in serum, other body fluids, and tissues. In some disease states, an excess of light chains are produced by the antibody-forming cells. These free light chains, unassociated with gamma globulin molecules, can be found in a patient's body fluids and tissues. Measurement of the various amounts of the different types of light chains aids in the diagnosis of multiple myeloma (cancer of antibody-forming cells), lymphocytic neoplasms (cancer of lymphoid tissue), Waldenstrom's macroglobulinemia (increased production of large immunoglobulins), and connective tissue diseases such as rheumatoid arthritis or systemic lupus erythematosus. |
• Antigen and Control Anti-DNA Antibody (FDA Code: LSW / 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). |
• Antinuclear Antibody, Indirect Immunofluorescen (FDA Code: DHN / 866.5100) |
• Centromere Detector |
• Contract Assembly |
• Contract Manufacturing |
• Control Antigen Antinuclear Antibody (FDA Code: LKJ / 866.5100) |
• Control Antiserum Antigen FC Test (FDA Code: DBN / 866.5530) An immunoglobulin G (Fc fragment specific) immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the Fc (carbohydrate containing) fragment of immunoglobulin G (resulting from breakdown of immunoglobulin G antibodies) in urine, serum, and other body fluids. Measurement of immunoglobulin G Fc fragments aids in the diagnosis of plasma cell antibody-forming abnormalities, e.g., gamma heavy chain disease. |
• Control Antiserum Antigen FITC FC Test (FDA Code: DBK / 866.5530) |
• Control Antiserum/Antigen |
• Diagnostics Contract Research & Development |
• FAB Fragment Specific Control (FDA Code: DFK / 866.5520) An immunoglobulin G (Fab fragment specific) immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the Fab antigen-binding fragment resulting from breakdown of immunoglobulin G antibodies in urine, serum, and other body fluids. Measurement of Fab fragments of immunoglobulin G aids in the diagnosis of lymphoproliferative disorders, such as multiple myeloma (tumor of bone marrow cells), Waldenstrom's macroglobulinemia (increased immunoglobulin production by the spleen and bone marrow cells), and lymphoma (tumor of the lymphoid tissues). |
• FITC Conjugated Gamma Globulin (FDA Code: DAF / 866.5510) |
• FITC IgA Antisera (FDA Code: CZN / 866.5510) |
• Gamma Chain Specific Control (FDA Code: DFZ / 866.5510) |
• Gamma Globulin (FDA Code: DAH / 866.5510) |
• General Biological Serum |
• Giardia Spp. (FDA Code: MHI / 866.3220) |
• Human and Animal Sera (FDA Code: KIS / 864.2800) Animal and human sera are biological products, obtained from the blood of humans or other animals, that provide the necessary growth-promoting nutrients in a cell culture system. |
• IGA Control (FDA Code: CZP / 866.5510) |
• IgE Control (FDA Code: DGC / 866.5510) |
• Immunoglobulin G FC Fragment Specific Antisera (FDA Code: DAS / 866.5530) |
• Immunoglobulin M (IgM) (FDA Code: DFT / 866.5550) |
• Manual Anti-Human Serum |
• Monoclonal Antibody Test |
• Mu-chain Specific Antisera (FDA Code: DAO / 866.5550) |
• Peroxidase Conjucated IgG (FDA Code: DAA / 866.5510) |
• Reagent Contract Manufacturing |
• Secondary Antibody Test (FDA Code: KTS / 866.5510) |
• Streptococcus Pneumoniae Antisera (FDA Code: GWC / 866.3740) |
• Streptococcus Pneumoniae Fluorescent Antiserum (FDA Code: GWB / 866.3740) |
• Streptococcus Spp Antigen (FDA Code: GTY / 866.3740) |
• Streptococcus Spp Antiserum (FDA Code: GTZ / 866.3740) |
• Streptococcus Spp Groups Fluorescent Antiserum (FDA Code: GTX / 866.3740) |
• Total Triiodothyronine Radioimmunoassay (FDA Code: CDP / 862.1710) A total triiodothyronine test system is a device intended to measure the hormone triiodothyronine in serum and plasma. Measurements obtained by this device are used in the diagnosis and treatment of thyroid diseases such as hyperthyroidism. |