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Titlebook: Hepatitis B and D Protocols; Volume 1: Detection, Robert K. Hamatake,Johnson Y. N. Lau Book 2004 Humana Press 2004 Hepatitis.antigen.infect

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Quantitative Assay of Hepatitis B Surface Antigen in Serum or Plasma Using Laurell Electrophoresisomorphic particles, predominantly spherical and partly filamentous. Their diameter appears in negatively stained electron micrographs as approx 20 nm. HBsAg typically reaches serum concentrations between 30 and 100 μg/mL during the incubation phase before acute hepatitis B; in immunotolerant hepatit
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Detection of Serum HDV RNA by RT-PCRridae family (.). HDV is a defective negative-strand RNA virus that requires concurrent infection with the hepatitis B virus (HBV) to complete its replicative cycle. The 36-nm virion consists of the delta antigen (HDV Ag) and the RNA genome of 1.6 kb within an envelop of surface antigen (HBsAg), pro
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Nonradioisotopic , Hybridization for HDV RNA sections (.). The method used a 27-mer end-labeled with digoxigenin (DIG). Hybrids were detected by a specific antibody coupled to alkaline phosphatase. Earlier reports had described the detection of both genomic and antigenomic HDV RNA by radioactive .S-labeled RNA probes (.) (.). However, because
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Immunohistochemical Detection of Hepatitis Delta Antigen is a phosphoprotein encoded by an open reading frame conserved among all HDV isolates. HDAg is a structural protein, because approx 200 subunits of HDAg bind via specific domains to genomic RNA, forming a core-like structure within an envelope provided by the co-infecting helper hepadnavirus (.). H
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HBV Vaccine-Escape Variantstermining antigenic distinctions among viruses, some limitations have been observed. For example, some viruses, such as measles and cytomegalovirus (CMV), do not have significant antigenic differences and cannot be divided into types and subtypes. In addition, serotyping does not usually have the ab
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A One-Filter–Three-Probe Assay for Defective Interference (DI) Effects of Naturally Occurring Core Iin a less than full-length genome and are replication-defective. They can be rescued by, and interfere with, the replication of homologous helper viruses. Another important characteristic of incomplete particles is their ability to enrich their proportion in the total viral yield in cells infected w
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Detection of Hypermodified Middle-Envelope (M) Proteins Secreted from Naturally Occurring HBV VarianRF) (.). This ORF contains three in-frame translational initiation AUG codons, dividing it into three regions: preS1, preS2, and S (.,.). The three envelope proteins are referred to in the literature as large (L) (p39/gp42), middle (M) (gp33/gp36), and small (S, major surface antigen) (p24/gp27) env
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