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英語人>網(wǎng)絡(luò)例句>RNA 相關(guān)的網(wǎng)絡(luò)例句
RNA相關(guān)的網(wǎng)絡(luò)例句
與 RNA 相關(guān)的網(wǎng)絡(luò)例句 [注:此內(nèi)容來源于網(wǎng)絡(luò)黄色真人免费网站,僅供參考]

Methods The BHD vector and the small interfer RNA targeting BHD was constructed and transfected into the cell line A549. The expression of BHD was examined by immunofluorescence. Transwell test was used to detect the invasion ability of A549 cells. Results After transfected BHD vector into A549 cells, immunofluorescence showed the expression of Folliculin located in cellular plasma.

制備BHD真核表達(dá)質(zhì)粒,轉(zhuǎn)染肺腺癌細(xì)胞www.色色色网,用免疫熒光法檢測Folliculin蛋白在肺癌細(xì)胞中的表達(dá)位置大桥未久黄色网站;篩選sRNAi片段,選取有效抑制片段轉(zhuǎn)入肺癌細(xì)胞点击进入a在线影院,與轉(zhuǎn)入BHD質(zhì)粒的肺癌細(xì)胞對比久久精品国产72精品,用Transwell實(shí)驗(yàn)了解BHD基因?qū)Ψ伟┘?xì)胞運(yùn)動方面的影響。

By using living cell imaging, time-lapse monitoring and FRAP technique, the intracellular behavior of poliovirus plus-strand RNA was studied in living host cells.

這一結(jié)果也證明了分子信標(biāo)是實(shí)現(xiàn)病毒核酸在活細(xì)胞內(nèi)可視化的有力工具色色碰精品。

Water solutions of RNAs were directly added to the mycelial colony of pine forest floor prior to fructification stage.

在形成子實(shí)體之前將RNA關(guān)聯(lián)物的水溶液直接灑入帶有菌絲群落的松樹林地表層丝袜美女诱惑久久国产。

HMW-GS1Dx5 gene specific expression in different times during wheat gemination was studied dy RNA dot blotmethods using HMW-GS1Dx5 gene probe.

利用小麥高分子量谷蛋白1D×5亞基探針,研究HMW-GS1D×5基因表達(dá)的規(guī)律偷拍人妻。

Objective To study the protein and mRNA expressions of transforming growth factor β in the human mesangial proliferative glomerulonephritis.

目的 探討轉(zhuǎn)化生長因子β蛋白及 m RNA基因在系膜增生性腎小球腎炎中的表達(dá)及其在發(fā)病中的作用。

The LV messenger ribonucleic acid levels of contractile and calcium regulatory genes were measured by quantitative real time polymerase chain reaction and normalized for glyceraldehyde 3-phosphate dehydrogenase.

采用定量實(shí)時(shí)聚合酶鏈反應(yīng)測定心室收縮蛋白和鈣調(diào)蛋白基因信使RNA水平又大又爽又深的欧美啪啪,采用3-磷酸甘油醛脫氫酶標(biāo)準(zhǔn)化无码强奷乱码中文字幕。

Methods The total RNA of leucocyte was extracted 43 allergic vasculitis patients and 24 normal subjects before and after treatment with Trizol reagent and the integrity and concentrations of HLA-DRw53 gene mRNA were determined by agarose gel electrophoresis and UV spectrophotometer after denatured with 1% formaldehyde, the product was transcribed into complementary retroviral synthetic deoxyribonucleic acid, and sequence-specific primers were designed based on the sequences of second HLA-DRw53 gene exon and housekeeping gene glyceraldehyde phosphate-dehydrogenase cDNA.

利用隨機(jī)引物逆轉(zhuǎn)錄合成互補(bǔ)脫氧核糖核酸,根據(jù)HLA-DRw53基因第二外顯子序列和管家基因人磷酸甘油醛脫氫酶的cDNA序列設(shè)計(jì)序列特異性引物。檢測43例變應(yīng)性血管炎患者治療前后與24名正常人HLA-DRw53基因mRNA表達(dá)量的變化人操人人插人。

Then folic acid targeted lipisome mediated MYCN siRNA(3.5mg/kg/day) was injected daily into tumor mass,continuously for 3 days, while same volume of normal saline, with the same protocol was injected in mice with control. Three hours after last day injection, all the mice were sacrificed, tumor mass was collected for MYCN and Glyceraldehyde phosphate dehydrogenase mRNA expression detection by real time RT-PCR.

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Objective\ To investigate the expression of cNOS mRNA in thyroid tissue of Graves' disease or Hashimoto's thyroiditis and its relationship with angiogenesis.

目的 研究 c NOS m RNA在格雷夫斯病和橋本甲狀腺炎甲狀腺組織中的表達(dá)及與血管形成的關(guān)系。

Brain RNA was extracted in cerebral cortex of rat embryo by guanidine isothiocyanate-phenol-chloroform method.

應(yīng)用實(shí)時(shí)定量PCR對nNOSmRNA精新在线三级电影视频、eNOSmRNA18禁无遮挡A片在线网站、iNOS mRNA的表達(dá)作相對定量分析。

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