| 1. | Gel filtration chromatography , gfc
凝胶过滤色谱法 |
| 2. | It was unadsorbed on cm - cellulose in 10mmol / l naac - hac ( ph 5 . 4 )
Sephadexg - 75凝胶过滤得到电泳级纯的凝集素。 |
| 3. | Gel filtration chromatography
凝胶过滤色谱法 |
| 4. | Sds - page and sephcryl s - 200 gel filtration detected the molecular weight of dnaase
利用sds page及sephacryl 200凝胶过滤测定分于量。 |
| 5. | At last , we got the pure protein with the determination of electrophoresis . the molecular weight of the enzyme is estimated at 30903 through gel filtration and sds - page electrophoresis . the isoelectric point is 8 . 6 ? . 3
经sds凝胶电泳和凝胶过滤层析两种方法测定该酶的分子量分别为33113dalton和28840dalton ；其等电点pi = 8 . 6 0 . 3 。 |
| 6. | In order to attain bioactive glycoprotein , glycoprotein of the leaves of camellia sinensis , was purified from coarse glycoproteins purified by sephadex g - 100 gel chromatography , by cona - sepharose 4b affinity chromatography
为了纯化天然糖蛋白，进行了茶树叶糖蛋白的cona - sepharose4b亲和层析，从sephadexg - 100凝胶过滤收集的粗糖蛋白中，分离茶树叶糖蛋白。 |
| 7. | The apparent molecular weight of g6pd , determined by gel filtration , was 220kd ; the subunit molecular weight was 50 . 5kd as determined by sds - page , suggesting that the native enzyme was a tetramer consisting of four identical subunits
凝胶过滤法测定该酶表观分子量约为220kd ， sds - page测定亚基分子量约为50 . 5kd ，可见该酶是由四个相同亚基构成的四聚体。 |
| 8. | The purified lectin showed a single protein band on sds - page , and the subunit molecular weight was 12kd . the molecular weight was 45kd determined by gel filtration on sephacryl s - 100 . the result implied that there are four same subunits per lra
经sds - page检测为单一蛋白带，亚基分子量为12kd ， sephacryls - 100凝胶过滤测得其表观分子量为45kd ，表明lra是由四个相同亚基组成的蛋白。 |
| 9. | Using i - dopa as a specific substrate , phenoloxidase ( po ) from penaeus chinensis hemolymph was purified by gel - filtration and ion - exchange chromatography , and characterized in terms of its molecular weight and enzymatic properties in this study
本文以中国对虾( penaeuschinensis )的血淋巴为材料，利用凝胶过滤和离子交换等方法，对酚氧化酶( phenoloxidase )进行了分离纯化和生物化学性质研究。 |
| 10. | Glycoproteins were detected from the elution of classified proteins by gel chromatography . glycoproteins from the leaves of camellia sinensis were respectively detected by preparatory quality of gel chromatography and glycoprotein staining in sds - gel
各分级蛋白进行sephadexg - 100凝胶过滤，使分级蛋白中的蛋白质按其分子量的大小先后洗脱，从每个分级蛋白凝胶过滤的收集液中，鉴定了茶树叶糖蛋白。 |
