Titlebook: Autoantibodies; Methods and Protocol Gunnar Houen Book 2019 Springer Science+Business Media, LLC, part of Springer Nature 2019 etiology.aut

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,Modellierung von Gesch?ftsprozessen,ng rodent tissue as substrate, the method was optimized by using the human immortal HEp-2 cell line derived from a larynx epidermal carcinoma. The HEp-2/IFA platform allows for optimal visualization of several cellular domains recognized by autoantibodies in the samples being tested. Serial dilution

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,Wesen von Gesch?ftsprozessen?,of laboratories that facilitate ANCA testing use commercial kits. Although in-house assays are not encouraged in routine clinical laboratories, knowledge on the methodological aspects of the assay remains of importance. These aspects include choice of substrate, choice of fixative, staining procedur

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https://doi.org/10.1007/978-3-8348-9005-4gged with a luciferase reporter. Here we describe LIPS assays for the quantification of autoantibodies to the H+, K+-ATPase A (ATP4A) and B (ATP4B) subunits, two serological markers of autoimmune atrophic gastritis and pernicious anemia. In particular, we will describe the expression of luciferase-t

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Fokus Mensch: Prozesse gekonnt beschreiben,is not detected in all SLE patients by routine laboratory tests. Looking at DNA–anti(ds)DNA interaction as one kind of DNA–protein interaction gave us the grounds for a novel type of assay, easy to perform, and providing a direct insight on DNA–anti(ds)DNA IgG interaction. The assay is an applicatio