Id |
Subject |
Object |
Predicate |
Lexical cue |
TextSentencer_T1 |
0-100 |
Sentence |
denotes |
Single cell studies of enzymatic hydrolysis of a tetramethylrhodamine labeled triglucoside in yeast. |
T1 |
0-100 |
Sentence |
denotes |
Single cell studies of enzymatic hydrolysis of a tetramethylrhodamine labeled triglucoside in yeast. |
T1 |
0-100 |
Sentence |
denotes |
Single cell studies of enzymatic hydrolysis of a tetramethylrhodamine labeled triglucoside in yeast. |
TextSentencer_T2 |
101-353 |
Sentence |
denotes |
Several hundred molecules of enzyme reaction products were detected in a single spheroplast from yeast cells incubated with a tetramethylrhodamine (TMR) labeled triglucoside, alpha-d-Glc(1-->2)alpha-d-Glc(1-->3)alpha-d-Glc-O(CH2)8CONHCH2- CH2NH- COTMR. |
T2 |
101-353 |
Sentence |
denotes |
Several hundred molecules of enzyme reaction products were detected in a single spheroplast from yeast cells incubated with a tetramethylrhodamine (TMR) labeled triglucoside, alpha-d-Glc(1-->2)alpha-d-Glc(1-->3)alpha-d-Glc-O(CH2)8CONHCH2- CH2NH- COTMR. |
T2 |
101-353 |
Sentence |
denotes |
Several hundred molecules of enzyme reaction products were detected in a single spheroplast from yeast cells incubated with a tetramethylrhodamine (TMR) labeled triglucoside, alpha-d-Glc(1-->2)alpha-d-Glc(1-->3)alpha-d-Glc-O(CH2)8CONHCH2- CH2NH- COTMR. |
TextSentencer_T3 |
354-533 |
Sentence |
denotes |
Product detection was accomplished using capillary electrophoresis and laser induced fluorescence following the introduction of a single spheroplast into the separation capillary. |
T3 |
354-533 |
Sentence |
denotes |
Product detection was accomplished using capillary electrophoresis and laser induced fluorescence following the introduction of a single spheroplast into the separation capillary. |
T3 |
354-533 |
Sentence |
denotes |
Product detection was accomplished using capillary electrophoresis and laser induced fluorescence following the introduction of a single spheroplast into the separation capillary. |
TextSentencer_T4 |
534-743 |
Sentence |
denotes |
The in vivo enzymatic hydrolysis of the TMR-trisaccharide involves at least two enzymes, limited by processing alpha-glucosidase I, producing TMR-disaccharide, TMR-monosaccharide, and the free TMR-linking arm. |
T4 |
534-743 |
Sentence |
denotes |
The in vivo enzymatic hydrolysis of the TMR-trisaccharide involves at least two enzymes, limited by processing alpha-glucosidase I, producing TMR-disaccharide, TMR-monosaccharide, and the free TMR-linking arm. |
T4 |
534-743 |
Sentence |
denotes |
The in vivo enzymatic hydrolysis of the TMR-trisaccharide involves at least two enzymes, limited by processing alpha-glucosidase I, producing TMR-disaccharide, TMR-monosaccharide, and the free TMR-linking arm. |
TextSentencer_T5 |
744-850 |
Sentence |
denotes |
Hydrolysis was reduced by preincubation of the cells with the processing enzyme inhibitor castanospermine. |
T5 |
744-850 |
Sentence |
denotes |
Hydrolysis was reduced by preincubation of the cells with the processing enzyme inhibitor castanospermine. |
T5 |
744-850 |
Sentence |
denotes |
Hydrolysis was reduced by preincubation of the cells with the processing enzyme inhibitor castanospermine. |
TextSentencer_T6 |
851-960 |
Sentence |
denotes |
Confocal laser scanning microscopy studies confirmed the uptake and internalization of fluorescent substrate. |
T6 |
851-960 |
Sentence |
denotes |
Confocal laser scanning microscopy studies confirmed the uptake and internalization of fluorescent substrate. |
T6 |
851-960 |
Sentence |
denotes |
Confocal laser scanning microscopy studies confirmed the uptake and internalization of fluorescent substrate. |
TextSentencer_T7 |
961-1079 |
Sentence |
denotes |
This single cell analysis methodology can be applied for the in vivo assay of any enzyme with a fluorescent substrate. |
T7 |
961-1079 |
Sentence |
denotes |
This single cell analysis methodology can be applied for the in vivo assay of any enzyme with a fluorescent substrate. |
T7 |
961-1079 |
Sentence |
denotes |
This single cell analysis methodology can be applied for the in vivo assay of any enzyme with a fluorescent substrate. |