immunofluorescence

Definitive diagnosis can be done by direct immunofluorescence or virus isolation.

It can also be achieved through indirect immunofluorescence assay.

Clinically the most widely used method is indirect immunofluorescence.

Indirect immunofluorescence assay is the principal test used to detect infection.

Plaque deposits are also visible through fluorescence and immunofluorescence microscopy.

Antibodies against this protein can be used to identify the nuclear envelope in immunofluorescence experiments.

In immunofluorescence, the level of autoantibodies is reported as a titre.

The immunofluorescence may then be observed with microscopy.

Localised disorders are best diagnosed by immunofluorescence of biopsy specimens.

Another widely used technique for detecting Lyme disease is the immunofluorescence assay.

Immunofluorescence staining was done by use of cells grown on coverslips.

A rapid immunofluorescence technique is also available in a small number of centres in Thailand.

Complement component 3 is seen under immunofluorescence.

The process of staining and mounting sample cells using indirect immunofluorescence is time consuming.

Immunofluorescence (IF) can be used to detect the virus in fetal organs.

Often, immunofluorescence microscopy can be used to visualize the immune complexes ).

Diagnosing PG is done by biopsy using direct immunofluorescence, appearance, and blood studies.

There they pioneered another new technique: immunofluorescence microscopy.

It is a necessary way to fix tissue for certain stain such as antibody linked immunofluorescence staining.

There are two classes of immunofluorescence techniques, primary (or direct) and secondary (or indirect).

Later studies using immunofluorescence microscopy of larger areas of tissue clarified diversity in earlier results.

Multiple immunofluorescence stains are performed to evaluate for antibody, protein and complement deposition.

All cells were fixed for immunofluorescence microscopy 10 min after addition of Dex.

Antineutrophil cytoplasmic antibody was measured in 31 patients by indirect immunofluorescence.

Immunofluorescence is usually negative.