| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-145 |
Sentence |
denotes |
Renaturation and ligand blotting of the major subunit of the rat asialoglycoprotein receptor after denaturing polyacrylamide gel electrophoresis. |
| T1 |
0-145 |
Sentence |
denotes |
Renaturation and ligand blotting of the major subunit of the rat asialoglycoprotein receptor after denaturing polyacrylamide gel electrophoresis. |
| TextSentencer_T2 |
146-286 |
Sentence |
denotes |
Rat hepatic asialoglycoprotein receptors (ASGP-Rs) bind terminal clustered galactosyl or N-acetylgalactosaminyl residues with high affinity. |
| T2 |
146-286 |
Sentence |
denotes |
Rat hepatic asialoglycoprotein receptors (ASGP-Rs) bind terminal clustered galactosyl or N-acetylgalactosaminyl residues with high affinity. |
| TextSentencer_T3 |
287-375 |
Sentence |
denotes |
The affinity-purified ASGP-R consists of three subunits designated RHL1, RHL2, and RHL3. |
| T3 |
287-375 |
Sentence |
denotes |
The affinity-purified ASGP-R consists of three subunits designated RHL1, RHL2, and RHL3. |
| TextSentencer_T4 |
376-621 |
Sentence |
denotes |
The ligand-binding activity of individual subunits was investigated by ligand blotting, after separation of subunits by SDS-PAGE under nonreducing conditions, electrotransfer to nitrocellulose, and incubation with 125I-asialo-orosomucoid (ASOR). |
| T4 |
376-621 |
Sentence |
denotes |
The ligand-binding activity of individual subunits was investigated by ligand blotting, after separation of subunits by SDS-PAGE under nonreducing conditions, electrotransfer to nitrocellulose, and incubation with 125I-asialo-orosomucoid (ASOR). |
| TextSentencer_T5 |
622-768 |
Sentence |
denotes |
No ligand-binding to any subunits could be detected when proteins such as BSA, casein, gelatin, or fat-free dry milk were used as blocking agents. |
| T5 |
622-768 |
Sentence |
denotes |
No ligand-binding to any subunits could be detected when proteins such as BSA, casein, gelatin, or fat-free dry milk were used as blocking agents. |
| TextSentencer_T6 |
769-899 |
Sentence |
denotes |
However, subsequent incubation of BSA-blocked nitrocellulose blots with some nonionic detergents resulted in renaturation of RHL1. |
| T6 |
769-899 |
Sentence |
denotes |
However, subsequent incubation of BSA-blocked nitrocellulose blots with some nonionic detergents resulted in renaturation of RHL1. |
| TextSentencer_T7 |
900-994 |
Sentence |
denotes |
125I-ASOR-binding to RHL2 or RHL3 was weaker and could be detected only after longer exposure. |
| T7 |
900-994 |
Sentence |
denotes |
125I-ASOR-binding to RHL2 or RHL3 was weaker and could be detected only after longer exposure. |
| TextSentencer_T8 |
995-1147 |
Sentence |
denotes |
Similarly, direct use of detergents such as Tween 20, Nonidet P-40, or Triton X-100 as blocking agents also preserved the ASOR-binding activity of RHL1. |
| T8 |
995-1147 |
Sentence |
denotes |
Similarly, direct use of detergents such as Tween 20, Nonidet P-40, or Triton X-100 as blocking agents also preserved the ASOR-binding activity of RHL1. |
| TextSentencer_T9 |
1148-1253 |
Sentence |
denotes |
Ionic detergents tested did not show any ability to renature the ligand-binding activity of RHL subunits. |
| T9 |
1148-1253 |
Sentence |
denotes |
Ionic detergents tested did not show any ability to renature the ligand-binding activity of RHL subunits. |
| TextSentencer_T10 |
1254-1478 |
Sentence |
denotes |
Among nonionic detergents tested, Tween 20, Tween 85, Lubrol PX, Nonidet P-40, and Triton X-100 were more effective than Tween 40, Tween 65, Tween 80, or Brij 35, whereas SPAN, digitonin, or octyl-glucoside showed no effect. |
| T10 |
1254-1478 |
Sentence |
denotes |
Among nonionic detergents tested, Tween 20, Tween 85, Lubrol PX, Nonidet P-40, and Triton X-100 were more effective than Tween 40, Tween 65, Tween 80, or Brij 35, whereas SPAN, digitonin, or octyl-glucoside showed no effect. |
| TextSentencer_T11 |
1479-1586 |
Sentence |
denotes |
Weak 125I-ASOR binding to RHL2 or RHL3 could be detected only when the Tween series or Lubrol PX were used. |
| T11 |
1479-1586 |
Sentence |
denotes |
Weak 125I-ASOR binding to RHL2 or RHL3 could be detected only when the Tween series or Lubrol PX were used. |
| TextSentencer_T12 |
1587-1676 |
Sentence |
denotes |
Incubation of blots with dithiothreitol caused a dose-dependent loss of binding activity. |
| T12 |
1587-1676 |
Sentence |
denotes |
Incubation of blots with dithiothreitol caused a dose-dependent loss of binding activity. |
| TextSentencer_T13 |
1677-1900 |
Sentence |
denotes |
The carbohydrate recognition domain (CRD) of RHL1, isolated after subtilisin digestion of ASGP-R bound to ASOR-Sepharose, retained ligand-binding activity as assessed by its binding to ASOR-Sepharose and by ligand blotting. |
| T13 |
1677-1900 |
Sentence |
denotes |
The carbohydrate recognition domain (CRD) of RHL1, isolated after subtilisin digestion of ASGP-R bound to ASOR-Sepharose, retained ligand-binding activity as assessed by its binding to ASOR-Sepharose and by ligand blotting. |
| TextSentencer_T14 |
1901-2014 |
Sentence |
denotes |
125I-ASOR binding to electroblotted CRD after SDS-PAGE was also dependent on the presence of nonionic detergents. |
| T14 |
1901-2014 |
Sentence |
denotes |
125I-ASOR binding to electroblotted CRD after SDS-PAGE was also dependent on the presence of nonionic detergents. |
| TextSentencer_T15 |
2015-2223 |
Sentence |
denotes |
We conclude that restoration of ligand-binding activity of RHL1 after SDS-PAGE by some nonionic detergents is not dependent on the presence of the cytoplasmic, transmembrane, or stalk domains of this subunit. |
| T15 |
2015-2223 |
Sentence |
denotes |
We conclude that restoration of ligand-binding activity of RHL1 after SDS-PAGE by some nonionic detergents is not dependent on the presence of the cytoplasmic, transmembrane, or stalk domains of this subunit. |