核素標記的 的英文怎麼說

中文拼音 [hésùbiāojìde]
核素標記的 英文
isotopically labeled
  • 核 : 核構詞成分。
  • 素 : Ⅰ形容詞1 （本色; 白色） white 2 （顏色單純） plain; simple; quiet 3 （本來的; 原有的） native Ⅱ名...
  • 標 : Ⅰ名詞1 [書面語] （樹梢） treetop; the tip of a tree2 （枝節或表面） symptom; outside appearance; ...
  • 記 : Ⅰ動詞1 （把印象保持在腦子里） remember; bear in mind; commit to memory 2 （記錄; 記載;登記） writ...
  • 的 : 4次方是 The fourth power of 2 is direction
  • 標記 : （標志; 記號; 貨物標記） tab; sign; stamp; peg; label; mark; flag; blip; notation; fleck; track; ...
  1. The effectiveness of the nuclear localization signal selected was clearly tested in initial experiments. based on this, the co - transfection systems used in the study was established. we first observed the multinucleate cells and chromatin bridges in cultured hela cells when the cells are marked with gfp and hochest33342, after co - transfection with the gfp expression plasmids and rnai plasmids rhe or rhc

    當分別共轉染附加kozac序列和核定位信號的gfp與人集縮素smc亞基hcap一e特異的rnai質粒rhe和人集縮素smc亞基hca屍一c的f { nai質粒rhc時，都觀察到gfp和hochest33342標記的轉染后hela細胞表現多核和染色質橋現象。
  2. The present results indicated that the paraventricular nucleus of the hypothalamus and the supraoptic nucleus might have important roles in neuroimmunomodulation. 2. following lps or seb was administered intraperitoneally, the expression of pcna of splenic cells and il - 1 receptor type i in pvn and son were observed by using immunocytochemistry in the mice. double fluorescent labeling technique was used to determine the relationship of il - 1 receptor type i co - expressions with arginine vasopressin or oxytocin

    二、小鼠腹腔內給予細菌內毒素lps或腸毒素seb ，用免疫組織化學方法觀察了脾臟核增殖抗體及下丘腦室旁核和視上核中1型il 1受體的表達，並採用雙標記技術觀察了1型il刁受體陽性神經元和加壓素及催產素表達的關系。
  3. The author reviewed the detection measures of prunus necrotic ringspot virus, and related the research progression of the pathogen detection technology inside and outside. the template amplication technology include pcr assays ^ nasba and so on. the cdna and crna probe which labeled with the isotope % biotin or dig, the offset probe and the peptide probe can be applied to magnify the signal. pcr - gene scan assays and pcr agilent chip chamber combine the template amplication and the signal magnification

    本文回顧了李壞死環斑病毒的檢測方法，較全面地評述了國內外病原物檢測技術研究進展：在模板的擴增有各種pcr技術、 nasba技術；在信號的放大有同位素、生物素或dig標記的cdna和crna探針，分支探針和肽核酸探針；模板擴增和信號放大相結合的有pcr -基因掃描技術、 pcr安捷倫晶元實驗室技術；模板擴增和雜交以及信號放大相結合的有pcr - elisa技術、實時熒光pcr技術、生物晶元技術。
  4. In order to further investigate the role of axudl in human tumor carcinogenesis and the potential association between the axudl gene expression status and the stimulation of transforming growth factor beta in human cancers, the present study was performed in three aspects as follows : ( 1 ) cloning full length enconding region cdna of axudl and construction of eukaryotic vector that expression the fusion protein of axud1 and influenza virus hemagglutin ha epitope tag ; ( 2 ) exploring the time and dose effects of tgf - 1 on the expression - of axudl gene in hepg2 hepatoma cells and spc - a1 lung carcinomas cells, and studying the effects of overexpression of axud1 on the expression of cell cycle and apoptosis related protein in hepg2 hepatoma cells ; ( 3 ) construction and expression of human axudl in e. coli m15. the following main results and conclusions can be obtained from the present study : 1. the full length ecnoding region of human axudl cdna from human peripheral blood lymphocytes was successfully cloned using one step rt - pcr method, and constructed into a eukaryotic expression vector which can be expressed a ha - axud1 fusion protein with axud1 and influenza virus hemagglutin ha epitope tag. the recombinant plasmid was identified by polymerase chain reaction, restriction endonuclease maping and sequencing, this expression vector might be instrumental to further study the function of axud1 protein in tumor cells

    為了進一步研究axud1在人類腫瘤發生中的作用及axud1基因的表達狀況與tgf -介導的信號通路的關系，本實驗研究分為三個部分： （ 1 ） axud1基因cdna全長編碼區的克隆和ha表位標記的axud1基因表達載體的構建； （ 2 ）探討肝癌細胞hepg2和肺腺癌spc - a1細胞中tgf - 1誘導的axud1基因表達的時間、劑量效應以及誘導表達的可能機理，並研究axud1的過表達對細胞周期和細胞凋亡相關蛋白表達的影響； （ 3 ） axud1原核表達載體的構建及其在大腸桿菌中的表達。本實驗的主要結果和結論如下： 1利用一步法rt - pcr成功地從人類外周血淋巴細胞中克隆出axud1基因編碼區cdna ，並將其構建入真核表達載體中，編碼的ha - axud1融合蛋白帶有流感病毒凝血素ha的表位標記肽段。
  5. 3 ) we tested total - family association, within - family association ( via tdt ), and linkage, between the bsrbl marker and bone phenotypes ( bmd and bone size ) at the spine and the hip ( femoral neck, torchanter and intertrochanter ) in chinese 402 nuclear families with a total number of 1263, and found the suggestive linkage ( p - 0. 037 ) between the il - 6 bsrbl maker and the li _ 4 spine bmd. no significant association and linkage was found for bone size and hip bmd. the present studies represented molecular genetic research of bone mineral density, and identified some factors related to bmd in chinese

    3 ）在徵集的402個核心家庭包括1263個個體組成的上海樣本中，利用傳遞不平衡檢測法（ tdt ） 、關聯分析和連鎖分析，檢測了白介素6基因和不同骨骼位點（腰椎、股骨頸、大轉子、轉子間區）的骨密度、骨大小之間的連鎖和/或關聯關系，並發現白介素6基因的bsrb工標記和控制腰椎骨密度的數量性狀位點（ qtl ）之間存在連鎖的證據（ p = 0 . 037 ） 。
  6. In this dissertation, we tried to improve the fairness of bandwidth sharing from two aspects : marking algorithm in diffserv and the implementation of tcp protocol. in summarize, this dissertation includes the following outcomes : 1 ) made a summarization that covers several models of quality of service ( qos ) provided in the internet, which include intserv, diffserv and mpls etc. this dissertation analysed the architecture and technological characteristics of each model. after an introduction of each model, the dissertation summarized what qos requests they can fulfil and how they implement them

    具體來說，本文的主要成果包括如下幾個方面： 1 ）對當前qos的幾個典型服務模型進行了綜述，指出了它們各自的優缺點，在此基礎上了，提出了一個端到端的qos體系結構，將現有的幾種服務模型集成起來，對網路資源進行有效地管理，使qos系統在核心網路具有很好的擴展性，同時在用戶網路或訪問網路能提供較精細的qos保證； 2 ）在標記演算法方面，本論文指出了影響帶寬共享公平性的幾個因素，分析了現有的標記演算法在公平性方面所存在的不足，在此基礎上，提出了一種自適應的公平數據包標記演算法（ adaptivefairmarker ， afm ） 。
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