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- SDS PAGE showed that the molecular weight of lumbrokinase is 26kDa. 经SDS 聚丙烯酰胺凝胶电泳 (PAGE)分析表明 ,表达的蚓激酶分子量为 2 6kDa。
- SDS PAGE analysis indicated that the expressed protein was about 30 kD. SDS PAGE分析 ,表达出约 30kD大小的蛋白 ;
- The activity of the SPG was detected by ELISA, and the purity and molecular weight of it were detected by SDS PAGE. 用ELISA法检测活性 ,用SDS PAGE检测纯度和相对分子质量
- No significant difference of protein separated by SDS PAGE was found between BDC and BBD groups. 胆管癌胆汁和良性胆汁蛋白SDS -PAGE谱基本相同。
- SDS PAGE analysis showed that the HLP 3 was almost purified with the molecular weight of 7kd. HLP?3为一7kd的单一多肽。
- SDS PAGE and thin layer scanning showed that the expressed product contained about 6.4% of total somatic protein. 经SDS PAGE和薄层扫描分析表明 ;外源蛋白表达量占菌体裂解蛋白总量的 6 .;4%25。
- SDS PAGE showed that the heavy chain and light chain of the eel serum Ig were 68kD and 26kD respectively. SDS -PAGE分析纯化的Ig ,显示欧洲鳗Ig重链约为 6 8kD、轻链约为 2 6kD。
- METHODS: Qualitative identification was made by IR, UV, AAS, PC, TLC,HPLC, amino acide analysis and SDS PAGE methods. 方法：采用红外、紫外、原子吸收光谱、氨基酸自动分析色谱及PC，TLC，HPLC，SDS?APGE电泳法进行定性鉴别。
- The sense clone was induced with IPTG. The expression of AcrA was observed on SDS PAGE. 经 IPTG诱导阳性菌 ,通过 SDS- PAGE检测出Acr A部分基因的表达
- Data of SDS PAGE showed that the molecular weight of PC and APC were about 38 kD and 33 kD , respectively. 经 SDS- PAGE测得 PC,APC的分子量分别约为 38,33k D
- Methods: The SDS PAGE and the radioisotope ( 59 Fe) was used in this investigation. 方法 :聚丙烯酰胺凝胶电泳 (SDS =PAGE)和放射性同位素法 (59Fe)。
- Results No significant difference of protein separated by SDS PAGE was found between BDC and BBD groups. 结果胆管癌胆汁和良性胆汁蛋白SDS-PAGE谱基本相同。
- Results The protein content of the purified EPF was 0.375 mg/ml,and a single band with a molecular weight of 26500 was observed on SDS PAGE profile. 以等电聚焦电泳法检测其等电点。 结果 从人流血中分离出EPF活性样物质 ;其蛋白含量为 0 .;375mg/ml;SDS PAGE见 1条均匀带;其相对分子质量为2 6 5 0 0;等电点为 6
- Objective:To isolate and purify melittin from bee venom and to establish an SDS PAGE and HPLC method for the determination of melittin content. 目的 :从蜜蜂毒中分离纯化蜂毒素 (melittin) ,建立以 SDS-聚丙烯酰胺凝胶电泳 (SDS- PAGE)及 HPL C进行蜂毒素定性定量分析的方法。
- SDS PAGE analysis demon strated that the enzyme was produced to the extent of as much as 38% of the total cellular protein. SDS PAGE分析表明 ;鸡肌腺苷酸激酶的含量可占大肠杆菌细胞总蛋白含量的 38%25 .
- SDS PAGE analysis revealed that the molecular weight of expressed product of TSV PA were 33kD. It was also proved by Western blot. SDS PAGE分析结果表明 ,表达产物为分子量 33kD的TSV PA蛋白 ,Western印迹分析也证实了此结果。
- SDS PAGE with silver staining showed about 85% purity of the isolated F o and 9 different subunits including b, OSCP, d, a, e, F 6, IF 1, A6L and c. SDS 聚丙烯酰胺凝胶电泳鉴定表明 ;纯化的Fo 含有b、OSCP (寡霉素敏感授予蛋白 )、d、a、e、F6、IF1、A6L和c等 9种亚基 .
- After determining the molecular weight of the purified protein by SDS PAGE, the band was excised from gel for protein identification. 经SDS PAGE测定纯化蛋白的分子量 ,然后切下目的蛋白条带 ,进行蛋白质鉴定。
- To study the difference between the Zmu 1:DHP guinea pig and Hartley guinea pig, the serum protein was analysed by the method of SDS PAGE. 为探讨不同品系豚鼠间的区别 ;对 Zmu- 1:DHP品系豚鼠和 Hartley品系豚鼠的血清蛋白质进行 SDS-聚丙烯酰胺凝胶电泳测定 .
- The changes in protein patterns were monitored with SDS PAGE and IEF/2D during callus proliferation and adventitious bud differentiation of Populus euphratica. 利用十二烷基磺酸钠聚丙烯酰胺凝胶电泳 (SDS PAGE)和等电聚焦双向电泳 (IEF 2D)对胡杨不同类型愈伤组织和愈伤组织分化不定芽过程中表达的蛋白进行了研究。
