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Human thyroglobulin reference material (CRM 457). 2nd part: Physicochemical characterization and certification

  • U. Feldt-Rasmussen*
  • , C. Profilis
  • , E. Colinet
  • , E. Black
  • , H. Bornet
  • , P. Bourdoux
  • , P. Carayon
  • , U. B. Ericsson
  • , D. A. Koutras
  • , L. Lamas de Leon
  • , P. DeNayer
  • , F. Pacini
  • , G. Palumbo
  • , A. Santos
  • , M. Schlumberger
  • , C. Seidel
  • , A. J. van Herle
  • , J. J. M. DeVijlder
  • *Corresponding author for this work
  • University of Copenhagen
  • Community Bureau of Reference
  • University Hospitals Birmingham NHS Foundation Trust
  • Universite Claude Bernard Lyon 1
  • Queen Fabiola Children's University Hospital
  • Lund University
  • Athens University Medical School
  • CSIC
  • Université catholique de Louvain
  • Cattedra di Endocrinologia
  • Instituto di Patologia Generale
  • Instituto Português de Oncologia de Lisboa Francisco Gentil E.P.E.
  • Institut Gustave Roussy
  • Henning Berlin
  • University of California at Los Angeles
  • Amsterdam UMC location University of Amsterdam

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

This report describes the characterization of a purified human thyroglobulin (Tg) reference material, and details the procedures used in its certification. The purified Tg is intended to be used as a primary reference material to establish calibration of working serum based reference material for immunoassay procedures. The programme involved the participation of 15 European laboratories and one laboratory from the United States. The physicochemical characterization showed by polyacrylamide gel electrophoresis and immunoblotting that the purified Tg had for the major part the expected molecular size of 660 kDa with traces of lower molecular forms. The amino acid composition was close to that demonstrated for the cDNA and the content of iodine was in keeping with a moderately to highly iodinated Tg. The mass concentration in reference material RM 457 is certified to be (0.324 ± 0.018) g/L on the basis of protein determined by the Lowry method and supported by nitrogen determination, absorbance measurement, and amino acid analysis. This reference material is considered the first step towards decreasing the interlaboratory variability between Tg methods of measurement.
Original languageEnglish
Pages (from-to)343-348
JournalAnnales de biologie clinique
Volume54
Issue number10-11
Publication statusPublished - 1996
Externally publishedYes

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