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公司成立于2001年,是丹麦一家专门生产抗体和基于抗体的各种生物产品的公司,目前公司员工有25人。公司致力于生产、销售高质量产品,并提供各种相关服务。
BioPorto拥有Bioporto Diagnostics和Antibody shop两个品牌,分别侧重于诊断试剂盒和抗体产品。在30多个国家有代理商,产品销售网络遍布全球,99%以上为出口销售。BioPorto Diagnostics旗下产品主要为几种临床快速诊断试剂盒,包括诊断早期急性肾损伤的NGAL ELISA kit,评估原发性免疫缺陷的MBL Oligomer ELISA kit,同时还有相关其他种属的科研用试剂盒和抗原抗体。其最新推出的产品有检测人体血浆中的活性蛋白C-蛋白C抑制物(APC-PCI)复合物的APC-PCI ELISA kit,高纯度人IgE单克隆抗体,以及Glucagon-like peptide-1和Exendin-4相关的单抗。