Content
Control Low, 3 x 1 mL and Control High, 3 x 1 mL
Form
Ready-to-use solution
Storage
Store at 2-8°C. Do not freeze
Shelf life
24 months at 2-8°C. See expiry date on the label
Storage after opening
4 weeks at 2-8°C, capped
Instructions
Measurements should be carried out in accordance with the specific application note for the automated chemistry analyzer used. Please see the Instructions for Use for The NGAL Test™ Reagent Kit ST001, which also give details of test principle and performance characteristics of The NGAL Test™.
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 and heparin plasma on automated clinical chemistry analyzers. The NGAL Test™ Control Kit contains control solutions to validate the calibration curve. NGAL measurements are useful in the diagnosis of acute kidney injury which may lead to acute renal failure.
Regulatory status
Not available in the USA for invitro diagnostic use. For in vitro diagnostic use in the European Union, Canada, Chile, Columbia, India, Korea, Russia, and Israel. For research use only in all other territories.
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。
