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CMV IgA

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Description

Product Information: CMV IgA

Product Name: CMV IgA (Cytomegalovirus Immunoglobulin A)

Overview: CMV IgA is a diagnostic immunoassay used to detect specific IgA antibodies against Cytomegalovirus (CMV) in human serum or plasma samples. Cytomegalovirus is a common virus that can cause infections in individuals with weakened immune systems, as well as newborns and pregnant women. The presence of CMV IgA antibodies can indicate an active or recent infection, aiding healthcare professionals in diagnosis and monitoring.

Key Features:

  • Type: Immunoassay (Enzyme-Linked Immunosorbent Assay, ELISA)
  • Purpose: Detection of CMV IgA antibodies in serum or plasma
  • Clinical Use: Diagnosis of CMV infections, especially in immunocompromised patients and pregnant women
  • Methodology: High sensitivity and specificity for IgA antibodies against CMV
  • Sample Type: Serum or Plasma
  • Test Time: Typically results within 1-2 hours
  • Storage Conditions: Store at 2-8°C; do not freeze

Indications:

  • Detection of recent or active CMV infections
  • Monitoring of CMV infections in immunocompromised patients, including organ transplant recipients and HIV-positive individuals
  • Assessment of risk in pregnant women, especially for fetal CMV transmission

Advantages:

  • Accurate Diagnosis: High specificity and sensitivity for CMV IgA antibodies.
  • Fast Results: Provides rapid and reliable results for clinical decision-making.
  • Non-invasive: Requires only a blood sample for testing.

Instructions for Use:

  1. Collect a serum or plasma sample.
  2. Prepare the sample according to the product’s guidelines.
  3. Run the immunoassay on the designated testing equipment (e.g., ELISA reader).
  4. Interpret the results based on the recommended reference ranges.

Results Interpretation:

  • Positive Result: Suggests recent or ongoing CMV infection.
  • Negative Result: Indicates the absence of detectable IgA antibodies against CMV, though it does not rule out a latent infection.
  • Equivocal Result: Further testing may be required to confirm the diagnosis.

Packaging:

  • Available in various kit sizes depending on the laboratory’s needs.
  • Includes reagents, controls, and instructions for use.

Precautions:

  • For in vitro diagnostic use only.
  • Ensure all reagents and samples are handled in accordance with laboratory safety protocols.
  • The test should be performed by trained personnel.

Conclusion: CMV IgA is an essential tool for the early detection of Cytomegalovirus infections, providing vital information for clinicians to make informed decisions regarding patient care. With its high sensitivity and rapid turnaround time, it supports effective management of CMV-related health issues, particularly in vulnerable populations.

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