查询词典 protein shock

There was a stastical difference of the expression of hTRT protein among well differentiated adenocarcinoma, poor differentiated adenocarcinoma and mucoid carcinoma. And there was a highly significant positive correlation between the expression of hTRT mRNA and hTRT protein. However, the expression of hTRT mRNA and its protein in GC were not related with other clinicopathological parameters including gender, age, location and size of neoplasm, wall invasion, lymph node metastasis and clinical stage.

结果：1。在53例GC中hTRTmRNA及hTRT蛋白表达均显著高于癌旁组织，hTRT蛋白表达在粘液癌与高分化腺癌和低分化腺癌间表达有显著性差异，hTRTmRNA与hTRT蛋白的表达呈显著正相关，而hTRTmRNA、hTRT蛋白的表达与各临床病理参数包括性别、年龄、肿瘤大小、部位、淋巴结转移、浸润深度及临床分期均无相关性； 2。

Protein protein interactions play vital roles in numerous biological processes. These interactions often result in formation of insoluble and noncrystalline protein assemblies.

在这个研究中，杨俊和特拉华大学的同事Tatyana Polenova设计了一组新脉冲序列，他们用这组脉冲序列研究了用不同同位素标记的thioredoxin蛋白质组装体的分子内和分子间的界面。

As a result of the difference on protein quality, if cotton dregses of rice with the beans,not be two kinds of any raw material, unit protein uses value to the raise of the animal identical, use Pi Texun method consequently the appropriate price of the raw material that with respect to meeting overmeasure protein character needs.

由于蛋白质质量上的差异，并不是任何两种原料如棉粕与豆粕，单位蛋白质对动物的饲用价值完全相同，因而采用皮特逊法就会高估蛋白质品质差的原料的适宜价格。

To analyze WWP1 protein expression in clinical samples, we applied IHC technology to detect the level of WWP1 protein in 18 paired OSCC samples, our data represented different they had different protein pattern and location.

应用免疫组织染色法侦测18对成对口腔癌样本WWP1蛋白表现，发现不同的样本呈现不同的蛋白表现量，表现在细胞的位置也有所不同。

The effect of tat p53 on the growth of parasites was determined by counting the parasitemia changes between pre and post incubation of the fusion protein with the parasite culture for 12 h. results: tat p53 fusion protein could be transduced into p.f parasites, locating at trophozoit and late schizont stage, whereas p53 protein could not.

结果：tat p53融合蛋白可以突破红内期疟原虫各层细胞膜，进入虫体细胞内，并可根据荧光观察到融合蛋白主要分布在疟原虫滋养体和晚期裂殖体，而p53蛋白不能进入疟原虫内。

The effect of TATp53 on the growth of parasites was determined by counting the parasitemia changes between pre and postincubation of the fusion protein with the parasite culture for 12 h. RESULTS: TATp53 fusion protein could be transduced into P.f parasites, locating at trophozoit and lateschizont stage, whereas p53 protein could not.

结果：TATp53融合蛋白可以突破红内期疟原虫各层细胞膜，进入虫体细胞内，并可根据荧光观察到融合蛋白主要分布在疟原虫滋养体和晚期裂殖体，而p53蛋白不能进入疟原虫内。

It is prepared with phosphatide with excellent biocompatibility and cell compatibility as dispersant, protein and polysaccharide as medicine wrapping material and through co-agglomeration process with control proportion among protein, polysaccharide and bone morphogenetic protein.

它是利用具有良好的生物相容性与细胞相容性的磷脂类物质为分散剂，以蛋白、多糖为药物的包覆材料，通过控制蛋白、多糖的比例以及他们的混合体与骨形态发生蛋白的比例，采用共凝聚技术，获得粒径40～2000nm的水分散的骨形态发生蛋白注射制剂。

Protease treatment of the plasma membranes could abolish the binding but NaIO_4 and glycosidase could not, indicating that nsLTP144 bound to plasma membranes protein without carbohydrate moiety. Using the homobifunctional cross-linking regent bissuberate (BS~3) and rice plasma membranes incubated with ~(125)I-Trx-nsLTP144, we identified, after SDS-polyacrylamide gel electrophoresis and autoradiography, a putative protein receptor on the rice plasma membranes with the molecular mass around 60 kDa. NsLTP144 can not trigger extracelluar alkalization in arabidopsis, but can abolish the extracellular alkalization effect of phytopathogen elicitor cryptogein, suggesting that cryptogein and nsLTP144 may bind to the same membrane protein. In vitro pull-down assay showed that nsLTP144 interacted with OsCaM1, a possible extracellular calmodulin, implying that nsLTP144 and OsCaM1 could function in the same signal transduction pathway. These results shed light on revealing the roles of nsLTP in vivo and make it promising to finally characterize the plasma membranes receptor of nsLTP.

发现~(125)I-Trx-nsLTP144、~(125)I-Trx-nsLTP110与水稻细胞质膜均具有特异性结合，而且结合是饱和性的、可被竞争的，符合配体-受体结合的典型特征，同时用于对照实验的蛋白质~(125)I-Thioredoxin没有此特性，表明水稻细胞质膜上存在nsLTP的受体；利用可氧化糖基的NaIO_4和水解糖基的N\'-糖苷酶F处理水稻细胞质膜，再进行结合实验，结合活性几乎不受影响；而利用胰蛋白酶处理细胞膜则使得结合能力几乎完全丧失，表明其受体为没有经过糖基化修饰的蛋白质；利用交联剂BS~3交联配体一受体后，再进行SDS-PAGE分离和放射自显影，结果显示水稻细胞质膜上的nsLTP受体中有一个60kDa的蛋白质可以与nsLTP144发生特异性的结合，可能是其受体；细胞外碱化实验表明，nsLTP144不能促使拟南芥原生质体细胞培养液的细胞外碱化反应，却能猝灭来自植物病原菌的激发子Cryptogein刺激拟南芥原生质体产生的细胞外碱化反应，表明nsLTP和Cryptogein结合细胞膜上相同的位点，保护了植物细胞免受Cryptogein导致的细胞程序性死亡，并诱导系统获得性抗性的产生；体外Pull-down实验表明，nsLTP144和水稻的OsCaM1具有相互作用，暗示了nsLTP144和OsCaM1可能同在一个信号通路上起作用。

Total RNA was isolated from cultured human pigmental cells and mRNA was reversly transcribed into cDNA. Then PCR was used to amplify the TRP -2 coding region. The PCR product was cloned into pUC19 plasmid and sequenced, then subcloned into vector pGEX-4T-1. The TRP-2 protein was expressed hi E coli of DH5 a as fusion protein with glutathioneS-transferase induced by IPTG. The fusion protein was purified by glutathione resin column.

我们通过RT—PCR的方法扩增TRP—2编码基因，克隆至pUC19载体并测序，再亚克隆至GST融合表达载体pGEX—4T—1，转化大肠杆菌，IPTG诱导表达了GST/TRP—2融合蛋白，并分析鉴定表达蛋白的可溶性，最后第四军医大学硕士学位论文一用谷氨酚胺树脂柱纯化表达的蛋白。

After training by three protein superfamilies from PIR protein database,the precision of the classification of the unknown protein sequences can respectively achieve

通过对PIR数据库中三类家族的学习，该网络对未知蛋白质序列分类的准确率分别达到了98.9%，98.1%，97.8%。

You can do some assertiveness training.

你可以进行一些自信训练。

We were well on the path to making a rear-wheel-drive global platform," says Mays."

我们正致力于建立一个后轮驱动的平台，"Mays这样说道。"