Amresco Inc

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Web: http://www.amresco-inc.com
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Address: 30175 Solon Industrial Pkwy, Solon, Ohio 44139, USA
Phone: +1-(440)-349-1313 | Fax: +1-(440)-349-1182 | Map/Directions >>

Profile: Amresco Inc manufactures & supplies biochemical and re-agents. Our products are used for molecular biology, life sciences, clinical and histology areas of research. We concentrate on biotechnology, biopharmaceutical, diagnostics, research specialty chemicals and related areas. We offer acrylamides, detergents, agaroses, dyes & stains and amino acids.

The company was founded in 1976, has ~100 employees and is ISO 9001 certified.

FDA Registration Number: 1550222

32 Products/Services (Click for related suppliers)

• Acid, Hydroxyazobenzene-Benzoic, Albumin (FDA Code: CJZ / 862.1035)

An albumin test system is a device intended to measure the albumin concentration in serum and plasma. Albumin measurements are used in the diagnosis and treatment of numerous diseases involving primarily the liver or kidneys.

• Alkaline Picrate Creatinine Colorimetric Method (FDA Code: CGX / 862.1225)

A creatinine test system is a device intended to measure creatinine levels in plasma and urine. Creatinine measurements are used in the diagnosis and treatment of renal diseases, in monitoring renal dialysis, and as a calculation basis for measuring other urine analytes.

• Bilirubin Diazo Colorimetry Test (FDA Code: CIG / 862.1110)

A bilirubin (total or direct) test system is a device intended to measure the levels of bilirubin (total or direct) in plasma or serum. Measurements of the levels of bilirubin, an organic compound formed during the normal and abnormal distruction of red blood cells, if used in the diagnosis and treatment of liver, hemolytic hematological, and metabolic disorders, including hepatitis and gall bladder block.

• Blood Urea Nitrogen (BUN) Reagent

• Cholesterol Colorimetric Test (FDA Code: CGO / 862.1175)

A cholesterol (total) test system is a device intended to measure cholesterol in plasma and serum. Cholesterol measurements are used in the diagnosis and treatment of disorders involving excess cholesterol in the blood and lipid and lipoprotein metabolism disorders.

• Clearing Agent (FDA Code: KEM / 864.4010)

• Colorimetric Uric Acid Test (FDA Code: KNK / 862.1775)

A uric acid test system is a device intended to measure uric acid in serum, plasma, and urine. Measurements obtained by this device are used in the diagnosis and treatment of numerous renal and metabolic disorders, including renal failure, gout, leukemia, psoriasis, starvation or other wasting conditions, and of patients receiving cytotoxic drugs.

• Continuous Flow Sequential Multiple Chemistry Analyzer (FDA Code: JJC / 862.2150)

A continuous flow sequential multiple chemistry analyzer for clinical use is a modular analytical instrument intended to simultaneously perform multiple chemical procedures using the principles of automated continuous flow systems. This device is intended for use in conjunction with certain materials to measure a variety of analytes.

• Creatine Phosphate Kinase Reagent Test

• Cytology Test Kits

• Diagnostics Contract Research & Development

• Enzymatic Esterase-Oxidase, Cholesterol (FDA Code: CHH / 862.1175)

• Fluorometric Calcium (FDA Code: JFO / 862.1145)

A calcium test system is a device intended to measure the total calcium level in serum. Calcium measurements are used in the diagnosis and treatment of parathyroid disease, a variety of bone diseases, chronic renal disease and tetany (intermittent muscular contractions or spasms).

• General Chemistry Calibrators

• General Chemistry Test Kits

• General Purpose Reagent (FDA Code: LDT)

• Ggtp L-Glutamylnitroanilide/Glycylglycine Test

• Glucose Oxidase, Glucose (FDA Code: CGA / 862.1345)

A glucose test system is a device intended to measure glucose quantitatively in blood and other body fluids. Glucose measurements are used in the diagnosis and treatment of carbohydrate metabolism disorders including diabetes mellitus, neonatal hypoglycemia, and idiopathic hypoglycemia, and of pancreatic islet cell carcinoma.

• Iron Reagent (FDA Code: CFM / 862.1410)

An iron (non-heme) test system is a device intended to measure iron (non-heme) in serum and plasma. Iron (non-heme) measurements are used in the diagnosis and treatment of diseases such as iron deficiency anemia, hemochromatosis (a disease associated with widespread deposit in the tissues of two iron-containing pigments, hemosiderin and hemofuscin, and characterized by pigmentation of the skin), and chronic renal disease.

• Lactate Dehydrogenase 4-dinitrophenylhydrazine 2 (FDA Code: CER / 862.1440)

A lactate dehydrogenase test system is a device intended to measure the activity of the enzyme lactate dehydrogenase in serum. Lactate dehydrogenase measurements are used in the diagnosis and treatment of liver diseases such as acute viral hepatitis, cirrhosis, and metastatic carcinoma of the liver, cardiac diseases such as myocardial infarction, and tumors of the lung or kidneys.

• Molecular Biology, Reagents

• Nitrophenylphosphate, Alkaline Phosphatase (FDA Code: CJE / 862.1050)

An alkaline phosphatase or isoenzymes test system is a device intended to measure alkaline phosphatase or its isoenzymes (a group of enzymes with similar biological activity) in serum or plasma. Measurements of alkaline phosphatase or its isoenzymes are used in the diagnosis and treatment of liver, bone, parathyroid, and intestinal diseases.

• Pharmaceuticals/Chemicals Contract Manufacturing

• Polyclonal Antibody

• Polyclonal Antibody Goat Anti-HbsAg IgG

• Polyclonal Antibody Goat Anti-human IgG

• Polyclonal Antibody Goat Anti-mouse IgG

• Polyclonal Antibody Goat Anti-rabbit IgG

• Polyclonal Antibody Goat Anti-whole hCG

• Reagent Contract Manufacturing

• Triglycerides Colorimetric Method Test (FDA Code: JGY / 862.1705)

A triglyceride test system is a device intended to measure triglyceride (neutral fat) in serum and plasma. Measurements obtained by this device are used in the diagnosis and treatment of patients with diabetes mellitus, nephrosis, liver obstruction, other diseases involving lipid metabolism, or various endocrine disorders.

• Urea Nitrogen Urease and Glutamic Dehydrogenase Test (FDA Code: CDQ / 862.1770)

A urea nitrogen test system is a device intended to measure urea nitrogen (an end-product of nitrogen metabolism) in whole blood, serum, plasma, and urine. Measurements obtained by this device are used in the diagnosis and treatment of certain renal and metabolic diseases.