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免疫化学

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There were five groups in the examination of cellular levelK562 group,K562/A02 group,K562+ADM group,K562/A02+ADM group and K562/A02+TTD+ADM group).The non-cytotoxicity doses to cell lines K562 and K562/A02 of TTD were got by MTT assay.Using flow cytometry (FCM assay to examine the intracellular ADM concentration.There were three groups in the examination of genic,zymologic and protein levelsK562 group,K562/A02 group and K562/A02+TTD group).The mRNA expression of MDR was measured by fluorescent quantitative reverse transcriptase polymerase chain reaction(RT-PCR.The expression levels of glutathione-S-transferase and topoisomerase Ⅱ were determined by immunohistochemical technique.

细胞水平检测实验分5组(K562组、K562/A02组、K562+ADM组、K562/A02+ADM组和K562/A02+TTD+ADM组),采用MTT法检测TTD对K562和K562/A02细胞的非细胞毒性剂量,流式细胞术检测细胞内阿霉素的浓度,基因、酶学、蛋白水平检测实验分3组(K562组、K562/A02组和K562/A02+TTD组),采用RT-PCR法检测mdr1 mRNA的表达,免疫细胞化学方法检测谷胱甘肽S转移酶π和拓扑异构酶Ⅱ的表达水平,Western-blotting法检测P-糖蛋白和bcl-2表达。

MATERAIL AND METHODS: The cell proliferation inhibition was measured by (3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromid,MTT) colorimetric assay. Morphological changes of EJ cells were observed by fluorescence staining of Hoechst 33258. Cell cycle and apoptosis were analyzed by flow cytometry.

材料与方法:四甲基偶氮唑蓝(3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromid,MTT)法检测EJ细胞增殖活力;荧光染色观察凋亡细胞的形态学变化;流式细胞术分析细胞周期及细胞凋亡;免疫细胞化学染色观察caspase-3 蛋白的表达。

In this study, the DNA fragments coding for amino acids 133~158 of VP1and 20~34 of VP4protein of type Asial FMDV were chemically synthesized and ligated into a tandem repeat 133~158-20~34-133~158. The sequences of signal peptide of Igκ chain and Kozak were fused to the 5'end of this tandem sequence and synthetic oligodeoxynucleotide containing CpG-ISS was fused to downstream of terminal coden of this tandem sequence. And then this long fragment was cloned into the eukaryotic expression plasmid pHook-2, forming a new secreted expression plasmid, named pAS1-E.

在第二章证明了亚洲Ⅰ型口蹄疫病毒VP1蛋白中133~158位氨基酸残基确是一重要B细胞中和抗原表位的基础上,依据第一章获得的口蹄疫病毒亚洲Ⅰ型VP1 cDNA序列及已报道Asial VP4序列,采用真核偏爱密码子化学合成了VP1中编码133~158位氨基酸及VP4中编码20~34位氨基酸这两个抗原表位基因,将其组成133~158-20~34-133~158串联结构,在其5′端加上鼠Igκ链信号肽序列,在翻译调节区加上增强表达的Kozak序列,同时在133~158-20~34-133~158串联结构3'端终止密码子下游加上CpG免疫刺激序列,将这些片段连接后,克隆到真核表达载体pHook-2上,构建成功了DNA疫苗重组表达载体pAS1-E。

Methods: The expression of Ki-67, E-Cad and nm23 in 52 cases of pituitary adenomas was examined by immunohistochemical methods.

应用免疫组织化学二步法同时检测3种蛋白在52例垂体腺瘤中的表达水平。

METHODS: Fresh human amnions were clipped to pieces which were sutured in a shape like muff by utilizing epidural tubes as a stent. When 4 cm section of ureter in length was excised to replace the defected ureter. 36 rabbit models were divided medially into the 1-month therapy and 3-month therapy groups. At the end of study, all amnion-ureter were sliced and examined with pathologic method or immunohistochemistry to check expressions of α-actin in smooth muscle cells and CKAE1/AE3 in transitional epithelial cells.

新鲜人羊膜裁剪成片状,以硬膜外导管为支架,做成袖套状,替代4 cm的大白兔输尿管缺损。36只成模大白兔均分为1个月治疗组和3个月治疗组,实验结束时,取羊膜输尿管行病理学检查和免疫组织化学检查平滑肌细胞α-Actin和移行上皮细胞CKAE1/AE3的表达情况。

Methods Using specific antiserums of NGF and BDNF by immunohistochemical ABC method.

方法采用免疫组织化学ABC法观察NGF和BDNF的改变。

The immunocytochemistry method was used to assay the expression of HnRNP A2/B1 in fiberobronchoscopic aspirates.

方法⒈ 利用免疫组织化学的方法检测56例经病理学确诊为肺癌的石蜡切片标本中HnRNP A2/B1的表达情况。

Methods The expression of HIF-1α was assayed by means of immunohistochemical technique in 60 patients.

方法通过免疫组织化学方法,了解HIF-1α在60例原发性颊黏膜鳞癌中的表达,分析其阳性表达水平与颊癌临床分期、病理分级以及预后等临床病理因素之间的关系。

A total of 14 autopsies were performed on patients treated by chemo-immunotherapy alone during the 1974-1976 period.

在1974-1976年间,对单独使用化学免疫治疗的14例患者进行尸检。

Grade Ⅳ is that the rat circumrotates to right in automatic action.②15 rats in each group were selected. 24 hours, 48 hours, one week after operation, we opened the skulls, took out the brain and used 2,3,5-Triphenyltetrazoluim Chloride staining to measure infarction volume, hematoxylin-eosin staining to observe the pathological change , and immunohistochemistry to detect the infiltration of CD34+ cells.

将两组大鼠各取15只,分别于术后24,48 h和1周开颅取脑,用2,3,5-氯化三苯基四氮唑染色测定脑梗死体积、苏木精-伊红染色检查脑组织病理变化、免疫组织化学检测CD34阳性细胞浸润情况。

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