Western Blot Results
A high titer means, therefore, a high level of antibodies and is likely to indicate a major response by the body to a current or recent infection.
Western blot results. The electrophoresis membrane is washed in a solution containing the primary antibody, before excess antibody is washed. Results from a Western blot test are usually reported in terms of titers which is a measure of the amount of dilution a sample needs before no antibodies remain detectable. A synthetic or animal-derived antibody is created that recognises and binds to a specific target protein.
The data produced with a Western blot is usually quite easy to interpret. In the majority of cases, bands corresponding to the target protein will become visible upon treatment of the blot with substrate. This type of test is a serological assay for detecting antibodies to Borrelia bacteria that cause Lyme disease.
The quantitative Western blot data were confirmed using p53 and IκBα ELISA assays (Assay Designs, Ann Arbor, MI). Schematic showing the assembly of a typical western blot apparatus with the position of the gel, transfer membrane, and direction of protein in relation to the electrode position. However, the Western blot is no longer used, and today.
In case of a positive result from this test, the ELISA test was previously followed by a test called a Western blot to confirm the diagnosis. The result is a membrane with a copy of the protein pattern that was originally in the polyacrylamide gel. In brief, the sample undergoes protein denaturation, followed by gel electrophoresis.
Densitometric analysis of the Western blots indicated that the linear range for IκBα was 0.097–3.12 ng and for p53 was 1.87–60 ng. 2.3.2 Results and discussion. The western blot, or western blotting, is a widely used analytical technique in molecular biology and immunogenetics to detect specific proteins in a sample of tissue homogenate or extract.
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