Test Method
Particle-enhanced turbidimetric immunoassay (PETIA)
Assay range
50 ng/mL to 3000 ng/mL (Can vary based on analyzer model)
Assay time
10 minutes (Hitachi 917) (Can vary based on analyzer model)
Content
1 x NGAL Buffer Solution (R1), 35 mL, 1 x NGAL latex suspension (R2), 7 mL
Form
Ready-to-use solution
Shelf life
24 months from manufacturing. See expiry date on the label
Storage after opening
Open vial stability 30 days, On board stability 30 days (when refrigerated)
Background
The NGAL Test™ is a particle-enhanced turbidimetric immunoassay for the quantitative determination of neutrophil gelatinase-associated lipocalin (NGAL) in human urine, EDTA plasma or heparin plasma on automated clinical chemistry analyzers. The NGAL Test™ Calibrator Kit contains calibrator solutions for establishing the calibration curve. NGAL measurements are useful in the diagnosis of acute kidney injury which may lead to acute renal failure.
Regulatory status
CE Marked and available for in vitro diagnostic use in the European Union, Canada, Korea and Israel. For research use only in all other territories.
Patent status
This product is protected by one or more US, European and/or foreign patents.
bioporto的NGAL Test™是一种颗粒增强的浊度免疫测定法，用于在自动化临床化学分析仪上定量测定人尿液，EDTA血浆或肝素血浆中的与中性粒细胞明胶酶相关的脂蛋白（NGAL）。NGAL Test™校准器套件包含用于建立校准曲线的校准器解决方案。NGAL测量可用于诊断可能导致急性肾衰竭的急性肾损伤。
