Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Cheng, Tsai-Mu | en_US |
dc.contributor.author | Pan, Ju-Pin | en_US |
dc.contributor.author | Lai, Shiau-Ting | en_US |
dc.contributor.author | Kao, Li-Pin | en_US |
dc.contributor.author | Lin, Hong-Huel | en_US |
dc.contributor.author | Mao, Simon J. T. | en_US |
dc.date.accessioned | 2014-12-08T15:13:25Z | - |
dc.date.available | 2014-12-08T15:13:25Z | - |
dc.date.issued | 2007-09-01 | en_US |
dc.identifier.issn | 0009-9120 | en_US |
dc.identifier.uri | http://dx.doi.org/10.1016/j.clinbiochem.2007.04.018 | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/10372 | - |
dc.description.abstract | Objectives: Haptoglobin (Hp) phenotypes 1-1, 2-1, and 2-2 are associated with inflammatory diseases. Since their biochemical structures are rather heterogeneous, it is necessary to accurately determine the plasma Hp levels. Design and methods: Immunodiffusion, immunoturbidimetric, and noncompetitive ELISA were conducted to determine the differences in immunoreactivity among Hp phenotypes and to verify that such difference may significantly affect the outcome of Hp determinations. A novel ELISA using phenotype-matched calibrators was performed to compared with a commercial GenWay ELISA kit using a single calibrator in normal healthy males. Results: In immunodiffusion and immunoturbidimetric assays, the immumoreactivity of Hp 1-1 was markedly higher than 2-1 and 2-2, while an opposite result was observed using an ELISA. The latter was primarily due to the repeated antigenic epitopes in polymeric 2-1 and 2-2. Thus, Hp levels could be significantly over- or underestimated depending on the method. An accurate ELISA could be achieved when using each type-specific Hp calibrator matched to each type subject. We show the mean levels of Hp 1-1 subjects (n= 16; 184 +/- 42 mg/dL) to be significantly and differentially greater than 2-1 (n=28; 153 +/- 55 mg/dL) (p < 0.05) and 2-2 (n=24; 93 +/- 54 mg/dL) (p < 0.01) subjects. Conclusions: Due to the diverse immunochemical structure among the Hp types, phenotyping should be performed in all the patients and a type-matched Hp calibrator should be used in clinical Hp determination. (c) 2007 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved. | en_US |
dc.language.iso | en_US | en_US |
dc.subject | ELISA | en_US |
dc.subject | imniunoreactivity | en_US |
dc.subject | haptoglobin phenotypes | en_US |
dc.subject | plasma concentration | en_US |
dc.subject | alpha(1)beta and alpha(2)beta chain expression | en_US |
dc.subject | HepG2 | en_US |
dc.title | Immunochemical property of human haptoglobin phenotypes: Determination of plasma haptoglobin using type-matched standards | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1016/j.clinbiochem.2007.04.018 | en_US |
dc.identifier.journal | CLINICAL BIOCHEMISTRY | en_US |
dc.citation.volume | 40 | en_US |
dc.citation.issue | 13-14 | en_US |
dc.citation.spage | 1045 | en_US |
dc.citation.epage | 1056 | en_US |
dc.contributor.department | 生物科技學院 | zh_TW |
dc.contributor.department | College of Biological Science and Technology | en_US |
dc.identifier.wosnumber | WOS:000249422200021 | - |
dc.citation.woscount | 7 | - |
Appears in Collections: | Articles |
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