Fig. 4.
Fig. 4. Sialidase, chlorate, or α-galactosidase treatment of WEHI-3 cells does not expose epitopes for mAbs to Lex or sLex. / Cells were untreated (control) or pretreated with sialidase, chlorate, both sialidase and chlorate, or α-galactosidase. (A) The cells were incubated with a nonbinding control IgM or with anti-sLexmAb CSLEX-1 or anti-Lex mAb MMA. Bound mAb was detected with FITC-conjugated goat F(ab)′2 fragments to murine IgM. (B) The cells were incubated with murine P- or E-selectin IgM chimera, followed by FITC-conjugated goat anti–human IgM. (C) The cells were incubated with FITC-conjugated GSI-B4 lectin, which recognizes α1-3–linked galactose residues, or with a nonbinding control IgM or anti-Lex mAb MMA. The data are representative of at least 4 experiments.

Sialidase, chlorate, or α-galactosidase treatment of WEHI-3 cells does not expose epitopes for mAbs to Lex or sLex.

Cells were untreated (control) or pretreated with sialidase, chlorate, both sialidase and chlorate, or α-galactosidase. (A) The cells were incubated with a nonbinding control IgM or with anti-sLexmAb CSLEX-1 or anti-Lex mAb MMA. Bound mAb was detected with FITC-conjugated goat F(ab)′2 fragments to murine IgM. (B) The cells were incubated with murine P- or E-selectin IgM chimera, followed by FITC-conjugated goat anti–human IgM. (C) The cells were incubated with FITC-conjugated GSI-B4 lectin, which recognizes α1-3–linked galactose residues, or with a nonbinding control IgM or anti-Lex mAb MMA. The data are representative of at least 4 experiments.

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