Previous Article | Next Article ![]()
Clinical and Diagnostic Laboratory Immunology, May 1996, 358-360, Vol 3, No. 3
GT Maine, T Lazzarotto, LE Chovan, R Flanders and MP Landini
In this work we used PCR to amplify the DNA regions coding for two
polypeptides from pUL57 of human cytomegalovirus (amino acids 540 to 601
and 1144 to 1233) and showed that both portions reacted very efficiently
with immunoglobulin M in sera of acutely infected subjects. However, pUL57
is not an essential antigen for the replacement of or supplement to a
cocktail of recombinant protein antigens containing portions of ppUL32,
-44, -83, and -80a in immunoglobulin M serology.
Copyright © 1996 by the American Society for Microbiology. All rights reserved.
The DNA-binding protein pUL57 of human cytomegalovirus: comparison of specific immunoglobulin M (IgM) reactivity with IgM reactivity to other major target antigens
Abbott Laboratories, Abbott Park, Illinois, USA.
This article has been cited by other articles:
| Antimicrob. Agents Chemother. | Clin. Microbiol. Rev. | Infect. Immun. |
|---|---|---|
| J. Clin. Microbiol. | J. Virol. | ALL ASM JOURNALS |