Thromb Haemost 1986; 55(02): 263-267
DOI: 10.1055/s-0038-1661533
Original Article
Schattauer GmbH Stuttgart

Visualization of von Willebrand Factor Multimers by Immunoenzymatic Stain Using Avidin-Biotin Peroxidase Complex

Authors

  • M Aihara

    The First Department of Internal Medicine, Hirosaki University School of Medicine, Hirosaki, Japan
  • Y Sawada

    The First Department of Internal Medicine, Hirosaki University School of Medicine, Hirosaki, Japan
  • K Ueno

    The First Department of Internal Medicine, Hirosaki University School of Medicine, Hirosaki, Japan
  • S Morimoto

    The First Department of Internal Medicine, Hirosaki University School of Medicine, Hirosaki, Japan
  • Y Yoshida

    The First Department of Internal Medicine, Hirosaki University School of Medicine, Hirosaki, Japan
  • M de Serres

    1   The Department of Pathology and Center for Thrombosis and Hemostasis, The University of North Carolina, Chapel Hill, NC, USA
  • H A Copper

    1   The Department of Pathology and Center for Thrombosis and Hemostasis, The University of North Carolina, Chapel Hill, NC, USA
  • R H Wegner

    1   The Department of Pathology and Center for Thrombosis and Hemostasis, The University of North Carolina, Chapel Hill, NC, USA
Further Information

Publication History

Received 07 January 1986

Accepted 18 February 1986

Publication Date:
18 July 2018 (online)

Preview

Summary

A technique for the detection of von Willebrand factor multimers separated by discontinuous SDS agarose electrophoresis has been developed using non-radioactive com-v pounds. The multimeric patterns were visualized by monospecific anti-human vWF:Ag followed by incubation with biotinylated antibody. After addition of avidin-biotin-peroxidase complex, the peroxidase activitiy was detected by 4-chloro-l-naphthol, giving sharp bands with a clear background.

By this method, the differences of vWF : Ag multimers could be easily observed between normal plasma and the plasmas from variant type vWD (IIA, IIB, platelet-type). Large and intermediate multimers were absent in the plasma with vWD type IIA, while only large multimers were absent in the plasma with vWD IIB and platelet-type. The absence of large multimers was also observed in two commercial F VIII preparations having the ratio of vWF/vWF : Ag 0.18 and 0.63. The preparation with the ratio of 0.63 showed the presence of larger intermediate multimers.

Electrophoresis in SDS 1.5% agarose gel revealed triplet structure of each small multimer, and a relative increase of the smallest subband was observed in vWD IIA plasma, platelet-type vWD plasma and commercial F VIII preparations.

The procedures described are easy and safe to perform and are useful for screening or classifying cases with vWD in general laboratories.