Id |
Subject |
Object |
Predicate |
Lexical cue |
T3374 |
0-4 |
Sentence |
denotes |
2.6. |
T83 |
0-4 |
Sentence |
denotes |
2.6. |
T3375 |
5-17 |
Sentence |
denotes |
Western Blot |
T84 |
5-17 |
Sentence |
denotes |
Western Blot |
T85 |
18-297 |
Sentence |
denotes |
To obtain total protein lysates, cells were homogenized in RIPA buffer (1% NP40, 0.5% sodium deoxycholate, 0.1% SDS, 1 mM EDTA, 1 mM EGTA, 1 mM Na3VO4, 20 mM NaF, 0.5 mM DTT, 1 mM PMSF, and protease inhibitor cocktail in PBS pH 7.4) and centrifuged at 12,000 g for 15 min at 4°C. |
T3376 |
18-394 |
Sentence |
denotes |
To obtain total protein lysates, cells were homogenized in RIPA buffer (1% NP40, 0.5% sodium deoxycholate, 0.1% SDS, 1 mM EDTA, 1 mM EGTA, 1 mM Na3VO4, 20 mM NaF, 0.5 mM DTT, 1 mM PMSF, and protease inhibitor cocktail in PBS pH 7.4) and centrifuged at 12,000 g for 15 min at 4°C. Protein concentrations were estimated by Coomassie Plus Protein Assay Reagent (Pierce, IL, USA). |
T86 |
298-394 |
Sentence |
denotes |
Protein concentrations were estimated by Coomassie Plus Protein Assay Reagent (Pierce, IL, USA). |
T3377 |
395-636 |
Sentence |
denotes |
Fifty micrograms of the resulting cytosolic protein extracts were heat-denatured in Laemmli sample loading buffer, separated by 10% sodium dodecyl sulfate polyacrylamide gel electrophoresis, and electroblotted onto a nitrocellulose membrane. |
T87 |
395-636 |
Sentence |
denotes |
Fifty micrograms of the resulting cytosolic protein extracts were heat-denatured in Laemmli sample loading buffer, separated by 10% sodium dodecyl sulfate polyacrylamide gel electrophoresis, and electroblotted onto a nitrocellulose membrane. |
T3378 |
637-942 |
Sentence |
denotes |
For immunoblotting, membranes were blocked with 5% nonfat dry milk in saline buffer overnight at 4°C, and the following antibodies were used: anti-β-actin (sc-130657, Santa Cruz Biotechnology, CA, USA, 43 kDa) and anti-matrix metallopeptidase 9 (MMP9) (sc-6841, Santa Cruz Biotechnology, CA, USA, 92 kDa). |
T88 |
637-942 |
Sentence |
denotes |
For immunoblotting, membranes were blocked with 5% nonfat dry milk in saline buffer overnight at 4°C, and the following antibodies were used: anti-β-actin (sc-130657, Santa Cruz Biotechnology, CA, USA, 43 kDa) and anti-matrix metallopeptidase 9 (MMP9) (sc-6841, Santa Cruz Biotechnology, CA, USA, 92 kDa). |
T3379 |
943-1066 |
Sentence |
denotes |
Each primary antibody was diluted appropriately in blocking buffer and then added to the blots for 1 h at room temperature. |
T89 |
943-1066 |
Sentence |
denotes |
Each primary antibody was diluted appropriately in blocking buffer and then added to the blots for 1 h at room temperature. |
T3380 |
1067-1224 |
Sentence |
denotes |
The blots were washed three times in the washing buffer and covered with the horseradish peroxidase-linked secondary antibody at a 1 : 2000 dilution for 1 h. |
T90 |
1067-1224 |
Sentence |
denotes |
The blots were washed three times in the washing buffer and covered with the horseradish peroxidase-linked secondary antibody at a 1 : 2000 dilution for 1 h. |
T3381 |
1225-1399 |
Sentence |
denotes |
Blots were incubated with enhanced chemiluminescence (ECL) detection system (Amersham Biosciences, Bucks, UK) and exposed to radiographic film (Fuji Hyperfilm, Tokyo, Japan). |
T91 |
1225-1399 |
Sentence |
denotes |
Blots were incubated with enhanced chemiluminescence (ECL) detection system (Amersham Biosciences, Bucks, UK) and exposed to radiographic film (Fuji Hyperfilm, Tokyo, Japan). |
T3382 |
1400-1454 |
Sentence |
denotes |
ImageJ was used to analyze the intensity of the blots. |
T92 |
1400-1454 |
Sentence |
denotes |
ImageJ was used to analyze the intensity of the blots. |
T3383 |
1455-1506 |
Sentence |
denotes |
The level of β-actin was used as internal standard. |
T93 |
1455-1506 |
Sentence |
denotes |
The level of β-actin was used as internal standard. |