Characterisation of the 1st SSI purified MBL standard

Clin Chim Acta. 2008 Sep;395(1-2):159-61. doi: 10.1016/j.cca.2008.06.006. Epub 2008 Jun 12.

Abstract

Background: Mannan-binding lectin (MBL) is of importance in innate immunity. MBL-deficiency, the most common immune defect, is significant in several clinical contexts. The request for MBL diagnostic is increasing, hence we developed a high-purity MBL standard assigned with a traceable value.

Methods and results: The standard material was produced from human plasma; and the protein concentration determined by amino acid analysis after a preceding desalting. The standard value was assessed by two series of sub-sample analyses from nine vials by the grand mean: 235.7 microg protein/ml (range 191.1-280.3 microg/ml). The loss during desalting was 7% and the protein content 253.4 microg/ml after correction. After SDS/PAGE the MBL content was estimated by densitometric scanning. The MBL band (non-MBL bands being MASPs) comprised 76%. Therefore, the standard was assigned a value of 192.6 microg MBL/ml (range 156.0-229.2 microg/ml). A calibrated time-resolved immuno-flourescence assay was used for stability evaluation of the MBL standard, after transfer from -80 degrees C, showing stability for at least 10 days at 25 degrees C, 14 days at 5 degrees C, and 16 weeks at -20 degrees C.

Conclusion: The 1st SSI purified MBL standard has been produced, and assigned the value 192.6 microg MBL/ml, traceable to an accurate realisation of the unit.

MeSH terms

  • Calibration
  • Electrophoresis, Polyacrylamide Gel
  • Fluoroimmunoassay
  • Humans
  • Mannose-Binding Lectin / blood
  • Mannose-Binding Lectin / isolation & purification*
  • Mannose-Binding Lectin / standards*
  • Molecular Weight
  • Reference Standards
  • Sensitivity and Specificity
  • Temperature
  • Time Factors

Substances

  • Mannose-Binding Lectin