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IgG2 subclass isotype antibody and intrauterine
IgG2 subclass isotype antibody and intrauterine

... In 1958, Franklin and Kunkel showed that only the IgG class of antibodies is transported across the placenta, which was later shown to be transported through receptor-mediated endocytosis by receptors specific for the Fc portion of the molecule10–13. Any transfer of IgG antibody molecule involves th ...
Implementation of Artificial Immune System Algorithms
Implementation of Artificial Immune System Algorithms

... suitable one. A number of AIS algorithms were examined and the AIRS2 algorithm was chosen due to its abilities to achieve high classification accuracies while possessing less computational complexity than other algorithms The choice between negative and positive selection can be based on various rea ...
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Trichomonas vaginalis

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Answer Key- Chapter 24 - Scarsdale Public Schools
Answer Key- Chapter 24 - Scarsdale Public Schools

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Theory and Practice of Immunocontraception in Wild Mammals
Theory and Practice of Immunocontraception in Wild Mammals

... Immunocontraceptionhas been proposed as a technique for managingwildlife populations in urbanand suburbansettingswhere traditional,lethal control methods may not be publicly acceptable. Immunocontraceptionuses an animal's own immune response to disruptreproductivefunction. Proteinsof eggs, sperm, fe ...
Memory B cells, but not long-lived plasma cells, possess antigen
Memory B cells, but not long-lived plasma cells, possess antigen

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Quantity, not quality, of antibody response decreased in the elderly
Quantity, not quality, of antibody response decreased in the elderly

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021709.JFantone.TypesI.IV.Immunopathology

... License: Unless otherwise noted, this material is made available under the terms of the Creative Commons Attribution–Non-commercial–Share Alike 3.0 License: http://creativecommons.org/licenses/by-nc-sa/3.0/ We have reviewed this material in accordance with U.S. Copyright Law and have tried to maximi ...
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... (抗毒素) to ...
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IMMUNOREACTIONS INVOLVING PLATELETS. VI. REACTIONS OF
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Rapid Diagnosis of Viral Infections
Rapid Diagnosis of Viral Infections

... swabs of genital lesions) show characteristic CPE often after only 24 to 48 hours of incubation. However, nongenital and low titer genital specimens may require incubation for several days prior to development of CPE. For these specimens, rapid HSV detection methods offer a distinct advantage. Varic ...
Cancer Immunity (6 February 2008) Vol. 8, p. 3 - Bio
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10Hypersensitivity Reaction
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An Introduction to Artificial Immune Systems
An Introduction to Artificial Immune Systems

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No Slide Title

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Immune Network: An Example of Complex Adaptive Systems
Immune Network: An Example of Complex Adaptive Systems

... (NIR) follows when the population of a foreign antigen in the body exceeds a tolerance level [10]. However, under special circumstances, the immune system mistakenly identifies a part of the host as a ”foreign” substance because of some ”error” [11]. Then, the immune response that follows against th ...
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ELISA



The enzyme-linked immunosorbent assay (ELISA) (/ɨˈlaɪzə/, /ˌiːˈlaɪzə/) is a test that uses antibodies and color change to identify a substance.ELISA is a popular format of ""wet-lab"" type analytic biochemistry assay that uses a solid-phase enzyme immunoassay (EIA) to detect the presence of a substance, usually an antigen, in a liquid sample or wet sample.The ELISA has been used as a diagnostic tool in medicine and plant pathology, as well as a quality-control check in various industries.Antigens from the sample are attached to a surface. Then, a further specific antibody is applied over the surface so it can bind to the antigen. This antibody is linked to an enzyme, and, in the final step, a substance containing the enzyme's substrate is added. The subsequent reaction produces a detectable signal, most commonly a color change in the substrate.Performing an ELISA involves at least one antibody with specificity for a particular antigen. The sample with an unknown amount of antigen is immobilized on a solid support (usually a polystyrene microtiter plate) either non-specifically (via adsorption to the surface) or specifically (via capture by another antibody specific to the same antigen, in a ""sandwich"" ELISA). After the antigen is immobilized, the detection antibody is added, forming a complex with the antigen. The detection antibody can be covalently linked to an enzyme, or can itself be detected by a secondary antibody that is linked to an enzyme through bioconjugation. Between each step, the plate is typically washed with a mild detergent solution to remove any proteins or antibodies that are non-specifically bound. After the final wash step, the plate is developed by adding an enzymatic substrate to produce a visible signal, which indicates the quantity of antigen in the sample.Of note, ELISA can perform other forms of ligand binding assays instead of strictly ""immuno"" assays, though the name carried the original ""immuno"" because of the common use and history of development of this method. The technique essentially requires any ligating reagent that can be immobilized on the solid phase along with a detection reagent that will bind specifically and use an enzyme to generate a signal that can be properly quantified. In between the washes, only the ligand and its specific binding counterparts remain specifically bound or ""immunosorbed"" by antigen-antibody interactions to the solid phase, while the nonspecific or unbound components are washed away. Unlike other spectrophotometric wet lab assay formats where the same reaction well (e.g. a cuvette) can be reused after washing, the ELISA plates have the reaction products immunosorbed on the solid phase which is part of the plate, and so are not easily reusable.
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