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Anti-Streptolysin O ASO Test Kit (Nephelometry Immunoassay Method)

Categories	kit swab samples
Model	pro
Instrument classification	Class I
Function	ASO Diagnosis
Application	Hosipital
Certificate	CE ISO
FOB port	Tianjin xingang
Terms of Payment	L/C, D/A, D/P, Western Union, MoneyGram, T/T, Paypal
Update Time	2022/6/30

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Anti-Streptolysin O ASO Test Kit (Nephelometry Immunoassay Method)

Quick Details

Model Number	Hipro
Origin	China
Instrument classification	Class I
Function	ASO Diagnosis
Certificate	CE ISO
Application	Hosipital

Product Description

[Intended Use]

This product is used to determine the content of Anti-Streptolysin"O"(ASO) in blood, and specific reagent for the specific protein analyzer, applies only to the clinical in vitro assisted diagnosis.

Streptolysin "O" is one of the metabolites of group A hemolytic streptococcus, a hemolytic activity of the protein, highly immunogenic. Hemolytic streptococcus group A in the human body exists as normal flora. The ASO has certain basic values in the normal human body. ASO increased after Hemolytic streptococcus infected. Therefore, ASO has become an important indicator to determine the streptococcal infection. Patients with Hypercholesterolemia or macroglobulinemia may also appear the ASO elevated.

[Principle]

The ASO units conjugated Anti-Streptolysin"O" (ASO) in the latex surface. ASO in the sample and the antibody become to immune complexes by Latex condensation reaction. The immune complexes will produce the phenomenon of light scattering, is proportional to the intensity of scattered light and samples of ASO levels. Using specific protein analyzer to measure the intensity of scattered light, the concentration of ASO is determined by comparing the turbidity of samples to the standard concentration.

[Sample Requirements]

Fresh serum samples, avoided hemolysis, store for 48 hours under 2-8 ℃.

[Range for Reference]

Normal reference range is 0~170 IU/ml.

Recommended that each laboratory establish its own reference range

[Limitations of the Method]

1. This product is based on latex agglutination system, only suitable for the specific analyzer.

2. This result for clinical reference only, comprehensive consideration should be combined with the clinical management of patients with symptoms / signs, medical history, other laboratory tests and treatment response.

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