Fig. 1. Specificity of the newly established MoAbs HSL11, HSL96, and HSL2 for human λ5, VpreB, and pre-BCR, respectively. A pre–B-cell line NALM6 (A), a pro–B-cell line RS4;11 (B), and X63.Ag8-653 cells transfected with either the λ5 or VpreB gene (C) were biosynthetically labeled with [35S]-methionine for 4 hours and lysed with 1% NP-40 lysis buffer. Detergent-soluble lysates were incubated with indicated MoAbs, and immunoprecipitates were analyzed by 13% SDS polyacrylamide gel electrophoresis under reducing conditions. The positions of μH, λ5, and VpreB are indicated by arrows, and a 16-kD band precipitated by HSL11 together with λ5 is indicated by an arrow head.
Fig. 1.

Specificity of the newly established MoAbs HSL11, HSL96, and HSL2 for human λ5, VpreB, and pre-BCR, respectively. A pre–B-cell line NALM6 (A), a pro–B-cell line RS4;11 (B), and X63.Ag8-653 cells transfected with either the λ5 or VpreB gene (C) were biosynthetically labeled with [35S]-methionine for 4 hours and lysed with 1% NP-40 lysis buffer. Detergent-soluble lysates were incubated with indicated MoAbs, and immunoprecipitates were analyzed by 13% SDS polyacrylamide gel electrophoresis under reducing conditions. The positions of μH, λ5, and VpreB are indicated by arrows, and a 16-kD band precipitated by HSL11 together with λ5 is indicated by an arrow head.

or Create an Account

Close Modal
Close Modal