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- macrophage expressed protein 巨噬细胞表达蛋白
- 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 ;
- In addition, the number of cells expressed MIF, particularly macrophage expressed MIF, may be used as a better predictor of LN activity and progressive renal injury. 结论 MIF在介导狼疮性肾炎病损中起重要作用，其上调表达可作为反映狼疮肾活动及进行性肾损害的指标。
- The results indicated that the 97 ku expressed protein could be recognized by CSFV positive serum as expected. 结果表明,IPTG诱导表达得到的pET-NS3融合蛋白的相对分子质量约为97 ku,与预期结果一致,且该重组蛋白能被CSFV阳性血清所识别。
- Expressed protein of recombinant pET- 30a- P30 were correctly identified by the application of mAb against T. gondii natural P30 antigen. 抗弓形虫天然P30的mAb能识别重组体pET-30a -P30的表达蛋白。
- The expressed protein yield reached 385mg/L in the 10L fermentor assayed by Coomassie brilliant blue stain G-250 method. 该条件用于指导小试（5L/10L罐），蛋白表达量达到了385mg/L；
- At the same time, the study also found differently expressed protein mass spectra among different grades of astrocytomas. 此外，在不同级别的星形细胞瘤之间也存在差异表达的蛋白峰。
- The molecular weight of SSIC expressed protein was about 31kDa and virus-like particles with diameter of about 22nm were formed. 在酵母中成功地进行了表达，表达产物(SSIC)的大小约为31kDa，并形成直径约为22nm的病毒样颗粒。
- SDS-PAGE profde showed a single protein band, and ELISA showed good antigenicity and specificity of the expressed protein. 获得的表达蛋白纯度达95%25，电泳显示单一条蛋白带，ELISA分析证实有较强的抗原性和较好的特异性。
- In order to express protein (RDE-4) of RNAi correctly, a pair of primers were designed in accordance with the reported RDE-4 gene sequences. 根据已报道的RDE-4基因序列;设计一对引物;从含C.
- The expressed protein was one-step purified to 97.53% using Ni-NTA affinity chromatography method under native condition, and with a yield of 18mg/L of induced culture. 表达产物经Ni-NTA亲和层析法一步纯化;蛋白纯度约达 97.;53%25;并可得到约18mg/L重组RTA蛋白。
- Objective: To observe the differentoial expressed protein spots in hypothalamus in yeast induced febrile rats and the yeast induced febrile rats treated with cinnamic aldehyde. 目的:观察桂皮醛对酵母致热大鼠的解热作用及其对下丘脑蛋白质组的影响。
- The expressed protein was purified by Glutath-one Sepharose 4B.A lot of target protein and a little of GST protein were obtained,the density of M2 was 5.6 mg/mL after defining the purification. 表达产物使用GST亲和吸附柱进行纯化;获得了大量的目的蛋白及微量的GST蛋白;使用分光光度仪确定纯化后M2蛋白的浓度约为5.;6 mg/mL。
- Methods The NBL stage-specific gene T668 was expressed in E. coli and the expression protein was used to immunize the mice at an interval of 10 days. 方法 以旋毛虫新生幼虫期特异性基因T6 6 8在大肠杆菌中的表达蛋白为抗原免疫小鼠 ,每间隔 10d免疫 1次 ,共免疫 3次。
- Expressed proteins as inclusion bodies were solubilized, refolded and purified by GST affinity chromatography. 表达产物为包涵体形式，溶解和折叠后，以GST亲合层析色谱纯化。
- Human macrophage stimulating protein，MSP Elisa... 人巨噬细胞刺激蛋白（MSP）试剂盒；
- Differentially expressed proteins were identified using Liquid Chromatography/Mass Spectrometry. 对差异表达的蛋白进行质谱分析。
- The result of SDS-PAGE indicated that the expression protein was about 40KD and reached to its peak at about 5 hours after inducing. SDS-PAGE电泳显示;表达的融合蛋白的分子量为40KD左右;且在诱导表达5小时后表达量最多;大约占菌体总蛋白的22.;4%25。
- Among the identified differential expression protein,the expression of DJ-1 protein was decreased in DADS-treated group. 与未处理组比较,初步鉴定的差异蛋白质DJ-1蛋白在处理组中表达下调,其功能与转录调节有关。
- The syndrome is marked by a reduction of maternally expressed proteins in a small section of chromosome 15, which is also usually paternally imprinted. 该病症以母方表达的15号染色体的一个小片断里的蛋白质减少为特点，15号染色体父方通常是印迹的（不表达）。
