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当前位置: 首页 > 产品中心 > Fluorescent_quantitative > bioporto/NGAL检测试剂盒/1kit/ST001
商品详细bioporto/NGAL检测试剂盒/1kit/ST001
bioporto/NGAL检测试剂盒/1kit/ST001
bioporto/NGAL检测试剂盒/1kit/ST001
商品编号: ST001
市场价: ¥0.00
美元价: 0.00
产地: 美国(厂家直采)
公司:
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍
Cat. No.
ST001
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.
品牌介绍
  丹麦Bioporto公司成立于2000年,致力于开发抗体产品及诊断试剂盒。2005年首次开发出NGAL ELISA 试剂盒,该产品于2006年获得欧盟CE认证,可用于急性肾功能损伤的临床诊断和监测。其目标是开发出更多的临床诊断专利产品。