Selling unit: per 100ml
Common name: Retinol Binding Protein ( RBP ) assay kit (latex-enhanced immunoturbidimetric assay)
English name: RBP Reagent Kit (Immunoturbidimetric Method)
3:1, 4:1, 5:1, common ratio 3:1, other ratios need to be customized
This kit is used to determine the level of human serum RBP.
RBP is a sensitive indicator of the nutritional status of the organism, especially protein-calorie malnutrition. Visceral protein is used as a traditional laboratory indicator of protein-energy malnutrition, while depending on the nutritional status retinol-binding protein RBP can provide a faster response.
RBP is mainly synthesized in the liver, so the decrease and increase of serum RBP is related to liver disease and influenced by the presence and severity of liver disease. In liver disease, serum RBP levels are significantly reduced in cirrhosis and in both acute and chronic hepatitis.
RBP can be used as an early diagnostic indicator of renal tubular injury. Retinol-binding protein RBP is stable in urine, not easily decomposed, and not disturbed by pH and blood pressure. In renal proximal tubular injury, its urinary excretion increases significantly, so the increase in urinary RBP excretion can be used as a marker of renal proximal tubular injury. When renal filtration function is reduced, blood RBP shows increased concentration due to storage. The concentration of RBP in blood or urine can be used as an ideal indicator of renal function in clinical practice.
The latex particles coated with polyclonal anti-human RBP antibody bind to the RBP antigen in the sample and form an immune complex, which is detected at 572 nm with a change in turbidity proportional to the RBP content in the sample.
Reagent components included in the product.
*Components are not interchangeable in kits with different lot numbers.
*Reagent components not included in the product, but necessary for the test: outsourced normal and abnormal QCs and calibrators.
Storage Conditions And Expiration Date
The kit is stored at 2-8°C away from light and is valid for one year.
Reagents that have been opened are taken care not to be contaminated and the reagents are stabilized in the instrument compartment (2-8°C) for one month.
The reagents must not be frozen.
Hitachi 7180/7600; Olympus AU680/2700; Toshiba TBA120; Myriad BS2000M/480; Siemens ADVIA 1800/2400 series automatic biochemical analyzers.
Fresh serum, if stored for a long time, should be stored frozen at – 20°C.
- Reagent preparation: liquid reagents are ready to use out of the bottle.
- test conditions: (different test instruments can be requested according to the different parameters on the machine)
*Reagents and sample volumes can be increased or decreased in proportion to the requirements of different biochemical analyzers as appropriate.
- Calibration procedure.
The use of matching calibrators is recommended.
- QC control procedures.
It is recommended that each laboratory establish its own quality control system and select appropriate quality control products for quality control. The measured values of QC products should be within the specified range. If outside the specified range, it is necessary to take appropriate measures or contact the manufacturer.
Using multi-point calibration, a standard curve was made with the calibrator concentration against the corresponding ΔA. The RBP concentration in the sample was read off the standard curve by the ΔA of the sample.
Positive Judgment Value Or Reference Interval
It is recommended that each laboratory establish its own reference range of normal values.
Interpretation Of Test Results
RBP measurement in serum is only one of the indicators used by clinicians to diagnose patients. Clinicians must also make a comprehensive judgment based on the patient’s physical symptoms, medical history, and other diagnostic items and diagnostic tools.
Limitations Of The Test Method
Bilirubin ≤ 20 mg/dL and hemoglobin ≤ 500 mg/dL did not interfere with the determination.
Product Performance Index
Absorbance of reagent blank: wavelength 572 nm, optical diameter 1.0 cm, temperature 37°C, A0 ≤ 1.0.
Analytical sensitivity: the absorbance change value △A ≥ 0.05 when the kit tests 50 mg/L of the test substance.
Linearity interval: test serum samples, reagent linearity in the interval of 3.5-150 mg/L, the linear correlation coefficient |r| should not be less than 0.990; in the interval of 3.5-20 mg/L, the absolute deviation of linearity should not exceed 2 mg/L; in the interval of (20- 150 mg/L, the relative deviation of linearity should not exceed ±10%.
Precision: repeatability CV ≤ 5%; relative extreme difference between batches ≤ 10%.
Accuracy: Relative deviation ≤ 10%.
- This product is for in vitro diagnosis only.
- To avoid absorption of proteins in glass containers, use plastic containers.
- 3. Avoid the formation of bubbles when handling samples and reagents and confirm that there are no air bubbles in the samples and reagents during the test.
- 4. Even samples that are negative for HBS antigen, HIV antigen, and HCV antibodies should be handled carefully and safely, as there may be a potential risk of infection.
- 5. The buffer solution and antiserum reagent contain sodium azide, which can react strongly with copper, lead and other metals to form azide metal, so please dilute the waste solution fully and flush the drain when discarded to avoid residue in the drain.
1 . Kanai M. et al: J Clin Invest,47,2025-2044 (1968).
- Kanai M. et al: Nippon Rinsho 57.279-281 (1999).