Adenosine Deaminase (ADA)
The assay is linear from 0-200 U/L and has precisions of Intra assay %CV < 4.5% and Inter assay %CV < 5.0%. The assay is ready-to-use for both manual method and automated chemistry analyzers (Kinetic). The assay is specific for ADA and has no detectable reaction with other nucleosides and is not affected by serum bilirubin up to 30 mg/dL, hemoglobin up to 200 mg/dL, triglycerides up to 750 mg/dL, or ascorbic acid up to 4 mg/dL. The assay is based on H2O2 detection, which is more sensitive and reliable than the method detecting ammonia production.
| Assay Principle
Diazyme's ADA Assay is based on the enzymatic deamination of adenosine to inosine which is 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-AA) in the presence of peroxidase (POD) to generate quinone dye which is monitored in a kinetic manner. The entire enzymatic reaction scheme is shown below.
Adenosine deaminase (ADA) assay kit is for determination of ADA activity in serum and plasma samples. For Research Use Only in the USA.
|Kit||DZ117A||R1/R2 (Dual Vial Liquid Stable)||Dual Vial Liquid Stable,
|Calibrator||DZ117A-Cal||Cal: 1 Level (Lyophilized)|
|Control||DZ117A-Con||Con: 2 Level (Lyophilized)|