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  2. Human herpesvirus 6 - Wikipedia

    en.wikipedia.org/wiki/Human_herpesvirus_6

    A low total IgG due to immune deficiency won't show increased titer levels. A singular rise in HHV-6 antibody levels may hint at an infection. Quest Diagnostics and ARUP Laboratories are known to provide IFA testing with specific median titer ranges. No IgM Screening Yes, present only during or shortly after active infection.

  3. Herpes - Wikipedia

    en.wikipedia.org/wiki/Herpes

    The older IgM serologic assay could not differentiate between antibodies generated in response to HSV-1 or HSV-2 infection. However, a glycoprotein G-specific (IgG) HSV test introduced in the 1980s is more than 98% specific at discriminating HSV-1 from HSV-2. [44]

  4. Herpes simplex virus - Wikipedia

    en.wikipedia.org/wiki/Herpes_simplex_virus

    Herpes virus DNA contains a gene for a protein called ICP4, which is an important transactivator of genes associated with lytic infection in HSV-1. [47] Elements surrounding the gene for ICP4 bind a protein known as the human neuronal protein neuronal restrictive silencing factor (NRSF) or human repressor element silencing transcription factor ...

  5. 6 Things You Need to Know About Herpes Tests, According to ...

    www.aol.com/news/6-things-know-herpes-tests...

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  6. Immunoglobulin G - Wikipedia

    en.wikipedia.org/wiki/Immunoglobulin_G

    The water-accessible surface area of an IgG antibody. Immunoglobulin G (IgG) is a type of antibody. Representing approximately 75% of serum antibodies in humans, IgG is the most common type of antibody found in blood circulation. [1] IgG molecules are created and released by plasma B cells. Each IgG antibody has two paratopes.

  7. Human betaherpesvirus 5 - Wikipedia

    en.wikipedia.org/wiki/Human_betaherpesvirus_5

    An ELISA technique for CMV-specific IgM is available, but may give false-positive results unless steps are taken to remove rheumatoid factor or most of the IgG antibody before the serum sample is tested. Because CMV-specific IgM may be produced in low levels in reactivated CMV infection, its presence is not always indicative of primary infection.

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