NORUDIA L-FABP
We created this page for medical staff.
- *Read carefully the package insert before use.
Assay Procedure
Reagent Preparation
- Reagent 1: L-FABP Buffer Solution 1 is ready to use.
- Reagent 2: L-FABP Latex Reagent 2 is ready to use.
Before using Reagent 2, gently invert the L-FABP Latex Reagent 2 bottle to mix thoroughly and check that no foam is formed.
Assay Procedure
This product is compatible with various types of automated analyzers. An example of the assay procedure is shown below.
- *1Use spot or pooled urine as the sample.
(do not use acidic urine or pooled urine containing toluene) - *2Absorbance Ⅰ and Ⅱ:Difference between absorbance at 570nm and at 800nm
Calibration material:L-FABP Calibrator (manufacture's assigned value)
Reagent blank:Saline
Assessment of Assay Results
- 1Correction of Assay Results
Assay results should be corrected for urinary creatinine concentration to calculate the L-FABP level (µg/gCr) per gram of urinary creatinine.
[Conversion formula] L-FABP(µg/gCr) = L-FABP(ng/mL) / Cr(mg/dL) × 100 - 2Reference Interva
The reference Interval calculated from the urinary L-FABP level in 412 healthy humans has been reported to be not more than 8.4 µg/gCr.6)
"NORUDIA" is a trademark or registered trademark of SEKISUI MEDICAL CO., LTD. in Japan and/or other countries.
We prepared this page for medical staff (doctors, dentists, pharmacists, clinical laboratory technicians, nurses, etc.) in Japan to ensure the correct use of our products. You should be aware that the information provided is not intended for overseas medical staff and the general public.