QUANTA Lite MPO IgG ELISA 708700 Inova Diagnostics Form

What is the QUANTA Lite MPO IgG ELISA 708700 Inova Diagnostics

The QUANTA Lite MPO IgG ELISA 708700 Inova Diagnostics is a diagnostic test designed to detect the presence of antibodies against myeloperoxidase (MPO) in the blood. This test is particularly relevant for identifying autoimmune conditions, such as vasculitis and other related disorders. The ELISA (enzyme-linked immunosorbent assay) format allows for a sensitive and specific measurement of IgG antibodies, providing valuable information for healthcare providers in diagnosing and managing patient conditions.

How to use the QUANTA Lite MPO IgG ELISA 708700 Inova Diagnostics

Using the QUANTA Lite MPO IgG ELISA 708700 requires careful adherence to the manufacturer's instructions. Typically, the process involves collecting a blood sample from the patient, which is then processed to isolate serum. The serum is added to a microplate coated with MPO antigens. After incubation, a secondary antibody conjugated with an enzyme is added, followed by a substrate that produces a measurable signal. The intensity of this signal correlates with the concentration of MPO antibodies present in the sample, allowing for quantitative analysis.

Steps to complete the QUANTA Lite MPO IgG ELISA 708700 Inova Diagnostics

Completing the QUANTA Lite MPO IgG ELISA 708700 involves several key steps:

• Collect a blood sample and allow it to clot to obtain serum.
• Prepare the assay reagents and microplate as per the kit instructions.
• Add the serum sample to the wells containing MPO antigens.
• Incubate the plate to allow for antibody binding.
• Wash the wells to remove unbound antibodies.
• Add the enzyme-linked secondary antibody and incubate again.
• Introduce the substrate solution and measure the optical density using a plate reader.

Legal use of the QUANTA Lite MPO IgG ELISA 708700 Inova Diagnostics

The legal use of the QUANTA Lite MPO IgG ELISA 708700 is governed by regulations surrounding medical diagnostics in the United States. Laboratories performing this test must comply with the Clinical Laboratory Improvement Amendments (CLIA) standards, ensuring quality and accuracy in testing. Additionally, the results obtained from this test should be used in conjunction with clinical evaluations and other diagnostic procedures to ensure comprehensive patient care.

Key elements of the QUANTA Lite MPO IgG ELISA 708700 Inova Diagnostics

Several key elements define the QUANTA Lite MPO IgG ELISA 708700:

• Specificity: The test is designed to specifically detect MPO antibodies, minimizing cross-reactivity with other antibodies.
• Sensitivity: The ELISA format allows for the detection of low concentrations of antibodies, making it effective for early diagnosis.
• Quantitative results: The test provides numerical values that help in assessing the severity of the autoimmune response.
• Ease of use: The test is designed for straightforward implementation in laboratory settings, facilitating efficient workflow.