Alpco Diagnostics

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Web: http://www.alpco.com
E-Mail:
Address: PO Box 451, Windham, New Hampshire 03087, USA
Phone: +1-(603)-893-8914 | Fax: +1-(603)-898-6854 | Map/Directions >>
 
 

Profile: Alpco Diagnostics imports and distributes medical research immunoassay kits. Our products are used in the clinical setting for in-vitro diagnostic purposes. We deliver an expanded line of vitamin assay kits. Our vitamin D assay kits are now available in either EIA or RIA format, for use in serum or plasma. Our Vitamin B6 REA kits are available in two sizes.

The company has revenues of USD 1-5 Million, has ~10 employees.

FDA Registration Number: 1222302

43 Products/Services (Click for related suppliers)  
• ACE
• ACE inhibitors
• ACTH
• ACTH Radioimmunoassay Test (FDA Code: CKG / 862.1025)
An adrenocorticotropic hormone (ACTH) test system is a device intended to measure adrenocorticotropic hormone in plasma and serum. ACTH measurements are used in the differential diagnosis and treatment of certain disorders of the adrenal glands such as Cushing's syndrome, adrenocortical insufficiency, and the ectopic ACTH syndrome.
• Angiotensin Converting Enzyme
• Angiotensin Converting Enzyme Radioassay (FDA Code: KQN / 862.1090)
An angiotensin converting enzyme (A.C.E.) test system is a device intended to measure the activity of angiotensin converting enzyme in serum and plasma. Measurements obtained by this device are used in the diagnosis and treatment of diseases such as sarcoidosis, a disease characterized by the formation of nodules in the lungs, bones, and skin, and Gaucher's disease, a hereditary disorder affecting the spleen.
• Angiotensin I and Renin Radioimmunoassay Test (FDA Code: CIB / 862.1085)
An angiotensin I and renin test system is a device intended to measure the level of angiotensin I generated by renin in plasma. Angiotensin I measurements are used in the diagnosis and treatment of certain types of hypertension.
• Angiotensin II
• Angiotensin II EIA Kit
• Auto-Immune Markers, CIC (C1-q)
• Beta-2 Microglobulin
• C Peptides of Proinsulin Radioimmunoassay Test (FDA Code: JKD / 862.1135)
A C-peptides of proinsulin test system is a device intended to measure C-peptides of proinsulin levels in serum, plasma, and urine. Measurements of C-peptides of proinsulin are used in the diagnosis and treatment of patients with abnormal insulin secretion, including diabetes mellitus.
• C- Reactive Protein
• C-Reactive Protein (CRP)
• C-Reactive Protein (CRP) Mouse ELISA Kit
• C-Reactive Protein (CRP) Rat ELISA KIT
• C-reactive Protein Assay
• Calcitonin RIA Kit
• Colorimetric Assay
• Diabetes and Obesity Immunoassay Kits
• EIA Auto-Immune Markers Extractable Nuclear Antigens
• ELISA Chemistry Analyzer
• ELISA Kits for Diabetes Assays
• Enzyme Immunoassay (EIA) Kits
• Enzyme Labeled Anti-DNA Antibody (FDA Code: LRM / 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).
• Estradiol
• Estradiol ELISA Kit
• Estrone-3 Glucuronide, Fertility Monitor
• GBM -Ab
• Human Chorionic Gonadotrophin EIA Kit
• Human Microalbumin Kit
• Immunoreactive Insulin Radioimmunoassay Test (FDA Code: CFP / 862.1405)
An immunoreactive insulin test system is a device intended to measure immunoreactive insulin in serum and plasma. Immunoreactive insulin measurements are used in the diagnosis and treatment of various carbohydrate metabolism disorders, including diabetes mellitus, and hypoglycemia.
• Myoglobin Ria Test Kit
• Progesterone
• Prolactin (rat) EIA Kit
• Prolactin ELISA Kit
• Prolactin Kit
• Rubella Enzyme Linked Immunoabsorbent Assay (FDA Code: LFX / 866.3510)
Rubella virus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to rubella virus in serum. The identification aids in the diagnosis of rubella (German measles) or confirmation of a person's immune status from past infections or immunizations and provides epidemiological information on German measles. Newborns infected in the uterus with rubella virus may be born with multiple congenital defects (rubella syndrome).
• Testosterone EIA Test Kit
• 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.
• Vascular Endothelial Growth Factor EIA
• Vitamin B12 Microbiological Test Kit
• Vitamin B12 Radioimmunoassay (FDA Code: CDD / 862.1810)
A vitamin B12test system is a device intended to measure vitamin B12in serum, plasma, and urine. Measurements obtained by this device are used in the diagnosis and treatment of anemias of gastrointestinal malabsorption.

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