Selling unit: per 100ml
- Common name: Immunoglobulin G (IgG) assay kit (immunoturbidimetric method)
- English name: IgG Reagent Kit (Immunoturbidimetric Method)
3:1, 4:1, 5:1, common ratio 5:1, other ratios need to be customized
This reagent is used to determine the content of IgG in human serum and plasma.
IgG is one of the most abundant immunoglobulins produced by plasma cells, accounting for 75% of total immunoglobulins. Its main function is to bind to antigens and further trigger their breakdown. decreases in IgG concentrations occur in primary and secondary immunodeficiency syndromes. Decreases may also be caused by loss of protein from the intestine or through scalded skin. Severe infections and autoimmune diseases can cause increased IgG concentrations, such as lupus erythematosus, infectious diseases and cholecystic fibrosis.
IgG and its corresponding antibody meet in the liquid phase to form insoluble immune complexes, resulting in turbidity in the reaction solution, and the turbidity level reflects the IgG content of the serum 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 careful not to be contaminated, and reagents are stable 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.
Plasma anticoagulated with serum or heparin or EDTA should be separated within 2 hours after blood collection and stored at room temperature (15-25°C) for 4 months and 2-8°C or -20°C for 8 months.
- Reagent preparation: liquid reagents are ready to use out of the bottle.
- test conditions: (different parameters on the machine can be requested according to different testing instruments)
Reagents and sample volumes can be increased or decreased in proportion to the requirements of different biochemical analyzers.
- Calibration procedure.
Landau calibrators are 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.
5 points are calibrated and the corresponding values are entered. With △A as the vertical coordinate and concentration as the horizontal coordinate, the standard curve is plotted, and this standard curve is corrected by the non-linear method Spline, Logit-Log4P and other modes, and this standard curve is saved and used to calculate the results.
Positive Judgment Value Or Reference Interval
7 to 16 g/L
It is recommended that each laboratory establish its own reference range of normal values.
Interpretation Of Test Results
Bilirubin ≤ 40 mg/dL, hemoglobin ≤ 500 mg/dL and celiac ≤ 500 mg/dL did not interfere with the determination.
Limitations Of The Test Method
The determination of IgG in human serum or plasma is only one of the indicators used by the clinician to make a diagnosis of the patient. The clinician must also make a comprehensive judgment based on the patient’s physical symptoms, medical history, and other diagnostic items and tools.
Product Performance Index
Absorbance of reagent blank: wavelength 700 nm, optical diameter 1.0 cm, temperature 37°C, A0 ≤ 0. 15.
Analytical sensitivity: the absorbance change value ΔA≥0.1 when the kit tests 20 g/L of the measured substance.
Linearity range: test serum samples, reagent linearity in the interval of 2~30 g/L, linear correlation coefficient|r| should not be less than 0.975; in the interval of 2~15 g/L, the absolute deviation of linearity should not exceed 1.5 g/L; in the interval of (15~30 g/L, the relative deviation of linearity should not exceed ±10%.
Precision: repeatability CV≤ 10.0%; relative extreme difference between batches≤ 15.0%.
Accuracy: Relative deviation ≤ 10%.
- This product is for in vitro diagnosis only.
- Avoid contamination when using the reagent, the container used must be clean, and please take necessary precautions, do not swallow, and avoid contact with skin and mucous membrane.
- Please dispose of the measured samples and waste liquids in accordance with the relevant national and local laws and regulations.
- For samples with lipid blood visible to the naked eye and triglyceride content exceeding 250 mg/dL, the results need to be diluted with saline before determination and multiplied by the dilution factor.
- Please dispose of the measured samples and waste liquids according to the relevant national and local laws and regulations.
- When changing the reagent lot number, the calibration should be re-calibrated.
- Gitlin D, Edelhoch HJ. Immunol. (1991); 66: 76-78.
- Burtis CA, Ashwood ER. Tietz Fund. Of Clin. Chem. 5thed. 30-54 and 462-494.
- Guder WG, Narayanan S, Wisser H, Zawta B. List of Analysis; Pre-analytical Variables. Brochure in: Samples: From the Patient to the Laboratory. Darmstadt: GIT Verlag. (1996).