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Pregnancy Rapid tests

Rubella IgG ELISA kit

Name

Rubella IgG ELISA kit

Category Name TORCH Panel
Test 96
Method ELISA method: Enzyme Linked Immunosorbent Assay
Principle ELISA priciple- Indirect; Antigen Coated Plate
Detection Range Qualitative elisa assay- Positive, Negative and Cut-off
Sample 5ul
Specificity 100%
Sensitivity 100%
Total Time 90 min
Shelf Life 12 months

Item #:                    1301Z   Quantity:               

Rubella IgG ELISA kit

 

Rubella IgG ELISA kit

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Rubella IgG ELISA kit description:




The Diagnostic Automation ELISA, Rubella IgG is intended for use in evaluating a patient's serologic
status to rubella virus infection. It is also used to evaluate paired sera for the presence of a significant increase in specific IgG as indicative of a recent or current rubella virus infection.

Rubella is a herpes virus. Generally rubella is considered a mild adolescence disease. However a maternal infection could be transmitted through the placenta to the fetus, causing congenital rubella. Congenital rubella may result in chronic cardiac disease, growth retardation, hepatosplenomegaly, malformations and other severe anomalies. Children born asymptomatic may develop these abnormalities later in life. To reduce risk of such severe complications, accurate serological methods must be performed to determine the serologic status of childbearing aged women. The presence of rubella specific IgG in the bloodstream attests immunity to rubella. A woman tested to be non-immune can be educated on the availability of vaccination. An increase in rubella IgG denotes an acute infection and differentiates rubella from other exanthematous diseases. Expecting women with current rubella infection should be counseled on the consequences of congenital infection.

Purified rubella antigen is coated on the surface of microwells. Diluted patient serum is added to wells, and the rubella IgG specific antibody, if present, binds to the antigen. All unbound materials are washed away. After adding enzyme conjugate, it binds to the antibody-antigen complex. Excess enzyme conjugate is washed off, and TMB Chromogenic substrate is added. The enzyme conjugate catalytic reaction is stopped at a specific time. The intensity of the color generated is proportional to the amount of IgG specific antibody in the sample. The results are read by a microwell reader compared in a parallel manner with calibrator and controls.