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'uric acid'

Items tagged with 'uric acid'

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Clinical Chemistry

Ready to use liquid stable reagents. Pack sizes cater to specific customer needs. High quality reagents manufactured to international standards. Categories: Clinical Chemistry, Reagents Description Reagents Technical Information KITS Albumin Alkaline Phosphatase AST/SGOT Bilirubin Direct Calcium CK-NAC Creatinine GGT LDL Direct Magnesium Total Protein Uric Acid ALT/SGPT Amylase Bilirubin Total Bilirubin Total & Direct Cholesterol CK-MB Glucose HDL Direct LDH-L Phosphorus Triglycerides Urea Kinetic (Rate BUN) Lipase information every single reagents has a diffrent price 1 pack single price.

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Clinical Chemistry

Infinite ADA 60 Diagnostic Reagent (R1 1 X 20ml: R2 1 X 10 ml) from Accurex. Infinite ADA reagent is used for direct quantitative determination of Adenosine deaminase (ADA) activity in human serum, plasma and other body fluids. The Reagent is a ready-to-use two liquid reagent system & can be performed in 11 minutes at 37° C. ADA is also know as Adenosine Deaminase which eliminates a molecule called deoxyadenosine, which is generated when DNA is broken down. About Infinite ADA is a reagent set for direct quantitative determination of Adenosine deaminase (ADA) activity in human serum, plasma and other body fluids. Infinite ADA is a ready-to-use, two liquid reagent system. With Infinite ADA, the assay is linear upto 200 U/L. Infinite ADA assay can be performed in 11 minutes at 37° C. Principle ADA catalyzes deamination of adenosine to inosine which is then converted to hypoxanthine by purine nucleoside phosphorylase (PNP). Hypoxanthine is then converted to uric acid and hydrogen peroxide (H2O2) by xanthine oxidase (XOD). H2O2 is further reacted with N-Ethyl-N-(2-hydroxy-3- sulfopropyl)-3-methylaniline (EHSPT) and 4-aminoantipyrine (4 AAP) in the presence of peroxidase (POD) to generate quinone dye. Quality Control To ensure adequate quality control, it is recommended that each laboratory should use a normal and an abnormal commercial reference control material. It should be realized that the use of quality control material checks both reagent and instrument functions together. Factors which might affect the performance of this test include instrument function, temperature control, cleanliness of glasswares and accuracy of pipetting. Other Details The reagents R1 & R2 are ready-to-use. The reagent kit should be stored at 2° – 8° C and is stable till the expiry date indicated on the label. Reagent R1 is light-sensitive & to be stored in dark. Contamination of the reagents should be strictly avoided.

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Clinical Chemistry

Acid Phosphatase Diagnostic Reagent (Pack size: 8 x 1 ml) from Accurex. Acid Phosphatase is used in accordance with ISO 14189 to detect acid phosphatase from Clostridium perfringens. Autozyme Acid Phosphate reagent is set for determination of Acid Phosphatase activity based on Kinetic method using a-naphthyl phosphate. In acidic pH of the buffer system, the reagent hydrolyses a-naphthyl phosphate to a-naphthol & phosphate. Accurex has gained considerable expertise in manufacturing & marketing of In-vitro Diagnostic reagents. About Autozyme Acid Phosphate is a reagent set for determination of Acid Phosphatase activity based on Kinetic method using a-naphthyl phosphate Autozyme Acid Phosphate is a single reagent system using one step procedure Autozyme Acid Phosphate can be determined in just 8 minutes at 37 degree C Acid Phosphate can be used on any Spectrophotometer, Discrete semi automated and Automated Analyzer. Programme can be designed for any specific analyzer upon request. Pack Size : 8 x 1 ml Principle In acidic pH of the buffer system, Acid Phosphatase hydrolyses a-naphthyl phosphate to a-naphthol and phosphate. The o-naphthol is then coupled with Diazotized Fast Red TR to form a Diazo dye which has strong absorbance at 405 nm. The increase in absorbance is directly proportional to the level of acid phosphatase in serum. The addition of L-Tartrate inhibits prostatic acid phosphatase but does not inhibit other isoenzymes. The activity of Prostatic Acid Phosphatase is obtained by subtracting the result of Non prostatic Acid phosphatase (Determination with Tartrate) from Total Acid Phosphatase (without tartrate). Quality Control To ensure adequate quality control it is recommended that each batch should include a normal and an abnormal commercial reference control serum. It should be realized that the use of quality control material checks both instrument and reagent functions together. Factors which might affect ne performance of this test includes proper instrument function, temperature control, cleanliness of glassware and accuracy of pipetting.

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Clinical Chemistry

The HumaStar 300SR is the latest member of HUMAN's clinical chemistry systems. Based on the proven hardware and software quality of HumaStar 100/200 it uses the time-tested system reagent kits of HumaStar 600 with perfectly matching methods, calibrators and controls. Throughput: up to 300 tests/h Sample positions: 60 Reagent positions: 40 Prefilled and validated system reagents 2 kit sizes per assay available Open channels: 3 Low water consumption (< 3 l/h) Intuitive and powerful software Multi-language: English, Spanish, French Intuitive and powerful software > Full traceability to reagents (e.g. lot & bottle), calibrations, users and settings > Searchable result database > Onboard and calibration stability monitoring > Automatic outlier detection and unit conversion > Method specific wash options > Designed for touchscreen Flexible system reagent concept > Plug & run HumaStar system reagents > Ready-to-use and available in two kit sizes > Usable for HumaStar 300SR and HumaStar 600 > Prefilled barcoded reagent bottles > Validated assay settings for highest quality > Up to 56 days reagent onboard stability > High quality reagents “Made in Germany” Eco-friendly ProClean 2.0 Technology > Minimal carry-over – dual solution wash station > Low water consumption – less than 3 l/h > Separation and reduction of biohazard waste Easy and efficient operation > Multi-step cuvette wash station for reaction cuvettes > Pre and post dilution for long walk-away time > Bottle cap holder prevents bottle mix-ups and saves time > Quick user- and service-friendly maintenance HUMAN‘s reagent production facility In Magdeburg, Germany we produce our reagents in accordance with the latest quality standards, guaranteeing consistent quality at the highest level. HUMAN Gesellschaft für Biochemica und Diagnostica mbH Max-Planck-Ring 21 · 65205 Wiesbaden · Germany Tel. +49 6122-9988-0 · Fax +49 6122-9988-100 · e-mail: human@human.de · www.human.de Immune Status anti-Streptolysin-O, Complement C3 and C4, CRP, Immunoglobulins IgA, IgG, IgM Liver Panel Albumin, Alkaline Phosphatase, Bilirubin Total and Direct, Cholinesterase, gamma-GT, GOT (ASAT), GPT (ALAT), Total Protein Kidney Panel Calcium, Creatinine, Cystatin-C, Inorganic Phosphorus, Magnesium, Microalbumin, Potassium, Sodium, Urea/BUN, Uric Acid, Urinary Total Protein Arteriosclerosis Cardiac Risk Assessment Cholesterol, HDL-/LDL-Cholesterol, Homocysteine, Triglycerides Anemia Iron, Total Iron Binding Capacity, Transferrin Pancreatic Tests alpha-Amylase, Lipase, Pancreatic Amylase Water & Electrolyte Balance Albumin, Chloride, Potassium, Sodium, Total Protein Cardiac Panel CK-NAC, CK-MB, GOT (ASAT), GPT (ALAT), Homocysteine, LDH Diabetes Glucose, HbA1c, Microalbumin, Triglycerides, Urinary Total Protein Prostata Acid Phosphatase HumaStar 300SR Broad range of clinical chemist

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Glucometer

Sinocare Blood Glucose Uric Acid Strips[Safe AQ UG] Pay attention to your body uric acid index. Fight Gout and Win💪 The validity period of blood glucose test strip is 24 months. Please use it within 6 months after opening the bottle. The validity period of uric acid test strip is 15 months. Please use it within 3 months. Warm Tips : Affected moderately by the environment humidity, the measured value will fluctuate by 15%, which is normal. Please try to store the test strips in an environment with moisture <80% to improve accuracy. Remove a new test strip within the valid expiration of the vial. After taking the strip, immediately cover the vial to avoid losing efficiency. Insert the test strip into the strip slot; the test strip is suggested to use in 3 minutes. Write the discard date (6 months after opening the vial) on the vial label when you open it for the first time. Discard the remaining test strips after the discard date. The test strips are for individual use only. Never reuse a test strip that has applied blood. Please don't store this blood glucose kit where it's too hot or cold. Keeping your fingers clean, wipe the first drop of blood away with a clean tissue, and test with the second drop of blood, which is less likely to be contaminated when using the testing kit. Adjust the depth of your lancing device according to your skin thickness when testing blood sugar.

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Glucometer

Sinocare Blood Glucose Uric Acid Meter with Advanced Test Strips Lancet Safe AQ UG for Multifunctions (82) Pay attention to your body uric acid index. Fight Gout and Win💪 Note: The validity period of blood glucose test strip is 24 months. Please use it within 6 months after opening the bottle. The validity period of uric acid test strip is 15 months. Please use it within 3 months. Warm Tips : Affected moderately by the environment humidity, the measured value will fluctuate by 15%, which is normal. Please try to store the test strips in an environment with moisture <80% to improve accuracy. Remove a new test strip within the valid expiration of the vial. After taking the strip, immediately cover the vial to avoid losing efficiency. Insert the test strip into the strip slot; the test strip is suggested to use in 3 minutes. Write the discard date (6 months after opening the vial) on the vial label when you open it for the first time. Discard the remaining test strips after the discard date. The test strips are for individual use only. Never reuse a test strip that has applied blood. Please don't store this blood glucose kit where it's too hot or cold. Keeping your fingers clean, wipe the first drop of blood away with a clean tissue, and test with the second drop of blood, which is less likely to be contaminated when using the testing kit. Adjust the depth of your lancing device according to your skin thickness when testing blood sugar.

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Clinical Chemistry

EM 360 is a Fully Automated Clinical Chemistry Analyser which is time tested and proven technology. It is designed to provide the most demanding productivity, speed and operational ease. EM 360 with a throughput of 360 tests/hour offers flexibility in operation and rugged performance to win against high workload, tight deadlines, multiple tasks and complexity of testing. It yields high quality results for virtually any biochemistry test to deliver quick, efficient and consistent performance. Product Features: Automated, Discrete, Patient prioritized, Floor model Based on proven technology, Diffraction Grating Separate probes for Reagent R1 & R2 and dedicated probe for sample Low reading volume of 200 µl only Onboard cooling for reagents to enhance the reagent stability Barcode for reagents & samples (Optional) Wide test menu Product Applications: End Point Reactions: Glucose, Cholesterol, Triglycerides, Albumin, Total Protein, Uric Acid, Calcium, Magnesium, Bilirubin Total, Bilirubin Direct Kinetic Reactions: SGOT, SGPT, GGT, LDH, CK, CK MB, ALP, ACP, Amylase, Lipase Two Point Rate Reactions: Urea, Creatinine Immunoturbidimetric Chemistries: RA, CRP, ASO, Direct HDL, Direct LDL, Apo A, ApoB, Lp (a) Special Chemistries: HbA1c, Iron, Ferritin, Phosphorus, Microprotein, Ammonia, Bicarbonates System Type: Discrete, automated, random access, patient prioritized clinical chemistry analyzer Throughput: 360 tests / hour photometric and 600 tests / hour with ISE* (*optional ISE with Na+, K+, Cl-, Li+) Analytical Methods: 1-Point, 2-Point, Rate-A, Rate-B, Direct Potentiometry (optional) Barcode Reader: For reagents and samples (optional) Reaction Tray: 60 hard glass cuvettes Reaction Mixing: Stirrer with variable speed Minimum reaction Volume: 150 μl with maximum 200 μl reading volume On-board Laundry: 5 stage cleaning, 2 stage drying Photometer: Multi-wavelength diffraction grating with 12 wavelengths (340, 376, 415, 450, 480, 505, 546, 570, 600, 660, 700, 750 nm) OD Range: 0.0 - 3.0 Light Source: Halogen lamp Detector: Silicon photo-diode Water Consumption: < 10 litres Programmable Parameters: Default system pack parameters + upto 99 user defined parameters, Unlimited profile and unlimited calculation items Quality Control: QC plot data with QC rules. Provision for lab mean. Twin plot Calibration: K-Factor, Linear (1, 2 point & multipoint), 4P and 5P Logit-log, cubic spline, exponential, polynomial, On-board serial dilution for calibrator Power Requirement: AC 220 V ± 10 %, 50 Hz or AC 110 V ± 10 %, 60 Hz Power Consumption: 800 VA Dimension (mm): Approx. 675 (W) x 840 (D) x 1120 (H) Weight: Approx. 150 kgs. SAMPLE HANDLING Sample: Serum, Plasma, Urine, CSF, Whole blood, other Sample Unit: 82 positions for samples, blank , controls, calibrators, STAT sample Sample Pipetting: 2 - 70 µl (adjustable in 0.1 µl step) for Biochemistry, 70 µl fixed for ISE Capacitance probe with liquid level sensing & vertical obstruction detection, serum indices Auto Rerun: Repeat with same, increased or decreased volume ( upto 1:150) Sample Tubes /Cups: Primary tubes of 5 ml, 7 ml, 10 ml and sample cups REAGENT HANDLING Reagent Tray: 50 positions for reagents with onboard cooling Reagent Pipetting: R1: 50 - 300 µl (adjustable in 1 µl step) R2: 10 - 200 µl (adjustable in 1 µl step) Capacitance probe with level sensing & vertical obstruction detection SYSTEM INTERFACE: Analyzer-PC: USB PC - Host Computer: Bidirectional TCP / IP & RS - 232 PC - Printer: USB Operating System: Windows Based Database: Unlimited Results

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immunoassayReagents

H-FABP Rapid Quantitative Test Finecare™ H-FABP Rapid Quantitative Test is a fluorescence immunoassay for quantitative measurement of Heart-type Fatty Acid Binding Protein (H-FABP) in human whole blood, serum or plasma. It is used for diagnosis of myocardial infarction.With original qualify control. STORAGE AND STABILITY 1. Store the test kit at 4℃~30℃ up to the expiration date printed on package. 2. If removed from refrigerator, allow the test kit for 30 minutes to return to room temperature before testing. 3. Do not remove the Test Cartridge from the pouch until use. The Test Cartridge should be used within 1 hour once opened.

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