| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-169 |
Sentence |
denotes |
Chromatographic resolution of glucosidic compounds, ginsenosides on polyethersulphone membrane, and its application to the quantitative immunoassay for ginseng saponins. |
| TextSentencer_T2 |
170-310 |
Sentence |
denotes |
A method has been devised for the chromatographic resolution of glucosidic compounds, ginseng saponins, on polyethersulphone (PES) membrane. |
| TextSentencer_T3 |
311-460 |
Sentence |
denotes |
The method results in good resolution and quantitative immunoassay for ginsenoside Rb1 (G-Rb1), G-Rc, and G-Rd in crude extracts of various ginsengs. |
| TextSentencer_T4 |
461-539 |
Sentence |
denotes |
The newly established method is simpler and applies for quantitative analysis. |
| TextSentencer_T5 |
540-773 |
Sentence |
denotes |
Ginsenosides developed by acetonitrile-water-acetic acid solvent system on a PES membrane were directly treated with a NaIO4 solution followed by bovine serum albumin (BSA), resulting in a ginsenoside-BSA conjugate on a PES membrane. |
| TextSentencer_T6 |
774-909 |
Sentence |
denotes |
Anti-G-Rb1 monoclonal antibody (MAb) was bound, and then a second antibody labeled with peroxidase directed against the first antibody. |
| TextSentencer_T7 |
910-970 |
Sentence |
denotes |
Finally a substrate reacted to the enzyme and gave staining. |
| TextSentencer_T8 |
971-1069 |
Sentence |
denotes |
The stained membrane was scanned, and spots were analyzed quantitatively using NIH Image software. |
| TextSentencer_T9 |
1070-1149 |
Sentence |
denotes |
At least 62.5 ng of G-Rb1, G-Rc, and G-Rd were clearly detectable individually. |
| TextSentencer_T10 |
1150-1229 |
Sentence |
denotes |
Three ginsenosides can be analyzed quantitatively between 0.125 and 2.0 microg. |
| T1 |
0-169 |
Sentence |
denotes |
Chromatographic resolution of glucosidic compounds, ginsenosides on polyethersulphone membrane, and its application to the quantitative immunoassay for ginseng saponins. |
| T2 |
170-310 |
Sentence |
denotes |
A method has been devised for the chromatographic resolution of glucosidic compounds, ginseng saponins, on polyethersulphone (PES) membrane. |
| T3 |
311-460 |
Sentence |
denotes |
The method results in good resolution and quantitative immunoassay for ginsenoside Rb1 (G-Rb1), G-Rc, and G-Rd in crude extracts of various ginsengs. |
| T4 |
461-539 |
Sentence |
denotes |
The newly established method is simpler and applies for quantitative analysis. |
| T5 |
540-773 |
Sentence |
denotes |
Ginsenosides developed by acetonitrile-water-acetic acid solvent system on a PES membrane were directly treated with a NaIO4 solution followed by bovine serum albumin (BSA), resulting in a ginsenoside-BSA conjugate on a PES membrane. |
| T6 |
774-909 |
Sentence |
denotes |
Anti-G-Rb1 monoclonal antibody (MAb) was bound, and then a second antibody labeled with peroxidase directed against the first antibody. |
| T7 |
910-970 |
Sentence |
denotes |
Finally a substrate reacted to the enzyme and gave staining. |
| T8 |
971-1069 |
Sentence |
denotes |
The stained membrane was scanned, and spots were analyzed quantitatively using NIH Image software. |
| T9 |
1070-1149 |
Sentence |
denotes |
At least 62.5 ng of G-Rb1, G-Rc, and G-Rd were clearly detectable individually. |
| T10 |
1150-1229 |
Sentence |
denotes |
Three ginsenosides can be analyzed quantitatively between 0.125 and 2.0 microg. |
| T1 |
0-169 |
Sentence |
denotes |
Chromatographic resolution of glucosidic compounds, ginsenosides on polyethersulphone membrane, and its application to the quantitative immunoassay for ginseng saponins. |
| T2 |
170-310 |
Sentence |
denotes |
A method has been devised for the chromatographic resolution of glucosidic compounds, ginseng saponins, on polyethersulphone (PES) membrane. |
| T3 |
311-460 |
Sentence |
denotes |
The method results in good resolution and quantitative immunoassay for ginsenoside Rb1 (G-Rb1), G-Rc, and G-Rd in crude extracts of various ginsengs. |
| T4 |
461-539 |
Sentence |
denotes |
The newly established method is simpler and applies for quantitative analysis. |
| T5 |
540-773 |
Sentence |
denotes |
Ginsenosides developed by acetonitrile-water-acetic acid solvent system on a PES membrane were directly treated with a NaIO4 solution followed by bovine serum albumin (BSA), resulting in a ginsenoside-BSA conjugate on a PES membrane. |
| T6 |
774-909 |
Sentence |
denotes |
Anti-G-Rb1 monoclonal antibody (MAb) was bound, and then a second antibody labeled with peroxidase directed against the first antibody. |
| T7 |
910-970 |
Sentence |
denotes |
Finally a substrate reacted to the enzyme and gave staining. |
| T8 |
971-1069 |
Sentence |
denotes |
The stained membrane was scanned, and spots were analyzed quantitatively using NIH Image software. |
| T9 |
1070-1149 |
Sentence |
denotes |
At least 62.5 ng of G-Rb1, G-Rc, and G-Rd were clearly detectable individually. |
| T10 |
1150-1229 |
Sentence |
denotes |
Three ginsenosides can be analyzed quantitatively between 0.125 and 2.0 microg. |