| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-67 |
Sentence |
denotes |
Antisera specificities to beta-D-galactopyranoside cluster ligands. |
| T1 |
0-67 |
Sentence |
denotes |
Antisera specificities to beta-D-galactopyranoside cluster ligands. |
| TextSentencer_T2 |
68-344 |
Sentence |
denotes |
Mono-, di-, and tri-beta-D-galactopyranosides of 2-(5-hydrazinocarbonylpentanamido)-2-(hydroxymethyl)-1,3-propan edi ol [(Gal)n-TA] have been conjugated to bovine serum albumin (BSA), and used to study the binding specificities to the Gal receptors of liver parenchymal cells. |
| T2 |
68-344 |
Sentence |
denotes |
Mono-, di-, and tri-beta-D-galactopyranosides of 2-(5-hydrazinocarbonylpentanamido)-2-(hydroxymethyl)-1,3-propan edi ol [(Gal)n-TA] have been conjugated to bovine serum albumin (BSA), and used to study the binding specificities to the Gal receptors of liver parenchymal cells. |
| TextSentencer_T3 |
345-622 |
Sentence |
denotes |
In this study, rabbit antisera produced to the (Gal)n-TA-BSA were characterized by using an enzyme-linked, immunosorbent assay under conditions that allow only the antibodies directed to the carbohydrate part of the antigen to react with the solid-phase (Gal)n-TA-BSA antigens. |
| T3 |
345-622 |
Sentence |
denotes |
In this study, rabbit antisera produced to the (Gal)n-TA-BSA were characterized by using an enzyme-linked, immunosorbent assay under conditions that allow only the antibodies directed to the carbohydrate part of the antigen to react with the solid-phase (Gal)n-TA-BSA antigens. |
| TextSentencer_T4 |
623-899 |
Sentence |
denotes |
Inhibition assays using (Gal)n-TA-BSA conjugates showed a relative specificity of the antisera for the number of Gal residues on the TA bridging group to the BSA carrier-protein, indicating that antibodies having specificities to oligosaccharide branch points can be produced. |
| T4 |
623-899 |
Sentence |
denotes |
Inhibition assays using (Gal)n-TA-BSA conjugates showed a relative specificity of the antisera for the number of Gal residues on the TA bridging group to the BSA carrier-protein, indicating that antibodies having specificities to oligosaccharide branch points can be produced. |
| TextSentencer_T5 |
900-1130 |
Sentence |
denotes |
Inhibition assays with (Gal)n-TA haptens, Gal, and methyl beta-D-Gal indicated that the antibody combining-sites interact mainly with the Gal units; no inhibition was observed with the TA bridging group used as a hapten inhibitor. |
| T5 |
900-1130 |
Sentence |
denotes |
Inhibition assays with (Gal)n-TA haptens, Gal, and methyl beta-D-Gal indicated that the antibody combining-sites interact mainly with the Gal units; no inhibition was observed with the TA bridging group used as a hapten inhibitor. |
| TextSentencer_T6 |
1131-1345 |
Sentence |
denotes |
The spatial distances of the Gal units were apparently important for interaction with the anti-(Gal)n-TA-BSA antibody-combining-sites, as (Lac)3-TA-BSA and (Lac)3-TA exhibited relatively little inhibitory activity. |
| T6 |
1131-1345 |
Sentence |
denotes |
The spatial distances of the Gal units were apparently important for interaction with the anti-(Gal)n-TA-BSA antibody-combining-sites, as (Lac)3-TA-BSA and (Lac)3-TA exhibited relatively little inhibitory activity. |
