細胞相關實驗 的英文怎麼說

中文拼音 [xìbāoxiāngguānshíyàn]
細胞相關實驗 英文
cell biology experiments
  • 細 : 形容詞1 （條狀物橫剖面小） thin; slender 2 （顆粒小） in small particles; fine 3 （音量小） thin ...
  • 胞 : Ⅰ名詞1 （胞衣） afterbirth2 （同一個國家或民族的人） fellow countryman; compatriot Ⅱ形容詞（同胞...
  • 相 : 相Ⅰ名詞1 （相貌; 外貌） looks; appearance 2 （坐、立等的姿態） bearing; posture 3 [物理學] （相位...
  • 關 : Ⅰ動詞1 （使開著的物體合攏） close; shut 2 （圈起來） shut in; lock up 3 （倒閉; 歇業） close down...
  • 實 : Ⅰ形容詞1 （內部完全填滿 沒有空隙） solid 2 （真實; 實在） true; real; honest Ⅱ名詞1 （實際; 事實...
  • 驗 : 動詞1. （察看; 查考） examine; check; test 2. （產生預期的效果） prove effective; produce the expected result
  • 細胞 : cell; sytes; bioplast; cella; [口語] gene; [生物學] cellule; cellule cellulli cellulo ; cello ; k...
  • 相關 : be interrelated; be related to; be bound up with; correlation; dependence; relevance; mutuality
  1. It can be concluded from the results that c - myc plays an important role in regulatin g the related genes in meiosis of spermatomeres and spermiogenesis and in regulating the secretion of the secretory cells in the spermatheca

    從實驗結果看， myc蛋白可能在減數分裂中激活相關基因，尤其是在精細胞形成早期可能參與了精細胞內大量的基因轉錄，還可能參與了受精囊囊壁上皮細胞的分泌活動。
  2. Researchers from the european molecular biology laboratory [ embl ] in grenoble and heidelberg, the institut de biologie structurale [ ibs ] and the unit of irus host cell interactions [ uhci ] *, both in grenoble, hae now produced the first 3 - dimensional image of part of this key protein

    現在，格勒諾布爾和海德堡的歐洲分子細胞學實驗室和格勒諾布爾的生物結構研究所及病毒宿主細胞相互作用部門的研究者們展示了部分這種關鍵蛋白質的首個三維影象
  3. In this research, the wheat, rice and tobacco with salt treatment were used as experimental materials to study the molecular mechanism of stress - tolerance in plant and make the relative gene engineering research. the main results are as following : 1. a novel ca2 + channel gene, named as tatpc1, was isolated from wheat, encoding a two - pore voltage - gated channel protein

    本研究在總結當前植物鹽脅迫應答分子生物學研究進展的基礎上，以農作物小麥、水稻、煙草作為主要實驗材料，開展了植物耐逆分子機制和相關基因工程研究，主要結果為： 1從小麥中克隆到一個新的ca ~ （ 2 + ）通道蛋白基因， tatpc1 ，它編碼的是一種細胞膜上兩孔電壓門控式通道蛋白。
  4. And hematopoietic progenitor assay was used to examine hematopoietic differentiation. the effect of mbmec - cm when combined with cytokines or mouse fetal liver stromal cell - conditional medium ( mflsc - cm ) on inducing es cells differentiation into hematopoietic cells was detected. the hematopoietic reconstitution of es cell - derived hscs was detected in vivo in irradiated recipient female mice

    實驗根據造血集落的形成、造血干祖細胞特異抗原和造血相關基因表達等方面檢測誘導生成的細胞是否含造血干祖細胞以及生成造血干祖細胞的數量，並且檢測誘導生成細胞的造血重建功能。
  5. Other experiments revealed slight variations in the size, number, arrangement, and interconnection of the nerve cells, but as far as psychoneuaral correlations were concerned, the obvious similarities of these sensory fields to each other seemed much more remarkable than any of the minute differences

    其他的實驗揭示神經細胞的大小、數量、排列和連接的細微變化，但就神經關聯而言，這些感覺區域的相似性比那些細微的區別更有意義可言。
  6. Methods to extend the migration of endothelial cells on sprouts from four directions - moving up, down, left or right - in previous models to random direction in the present model, and develop a relevant 2d discrete model to simulate the process of tumor angiogenesis and compare the simulation results with some corresponding experimental data

    方法將新生血管芽尖的內皮細胞遷移方向由先前模型的上、下、左、右四個方向擴展為任意方向，建立相應的二維離散模型，數值模擬實體腫瘤微脈管系統的生成過程，比較模擬結果與相關實驗數據的符合程度。
  7. In the third experiment, we first constructed a test model of differentiation from mouse es cells to cardiomyocytes. then series of dilutions of three chemicals were screened on this platform. the combination of all trans retinoic acid and dmso is employed as positive control

    實驗三首先建立了一個小鼠胚胎幹細胞定向分化成心肌細胞的實驗平臺，然後採用了3種心肌疾病相關的藥物：黃芑生脈飲、 1 ， 6二磷酸果糖和hg （代號） ，在此定向分化的實驗平臺上進行了一系列濃度的藥物篩選，實驗採用視黃酸和dmso的混合誘導劑作為陽性對照。
  8. Based on the data arising from the experiments in this thesis, a hypothesized model, which intends to explain the mechanisms and relationship between histone acetylation and the expression of important cell cycle regulating factors in physarum polycephalum. the main results and conclusions of this thesis are as follows. 1

    通過1 」 sa處理、 rt干cr和蛋白兔疫印跡實驗，發現多頭絨泡菌細胞中存在著哺乳動物細胞周期調控相關回于的同源物，包括細胞周期素類cyclinbi蛋白、癌基因產物類c foo和類c j 。
  9. The lung tissue for immunohistochemitry and laser scanning confocal microscopy were fixed and embedded. the morphological alteration of pulmonary neuroendocrine cells which stain for calcitonin gene - related peptide ( cgrp ), serotonin ( s - ht ) and luteinizing hormone ( lh ) were studied. the results of these were dealed with computer image analysis and statistical treatment

    肺組織取材后經固定、梯度酒精脫水、包埋、連續切片后，應用免疫組織化學方法、透射電鏡及激光掃描共聚焦技術觀察了降鈣素基因相關肽（ cgrp ） 、五羥色胺（ 5 - ht ） 、黃體生成素（ lh ）陽性細胞的隨齡變化，並對實驗結果進行了計算機圖像分析和統計學處理。
  10. Professor franky l chan of the department of anatomy explained, previous studies of prostate cancer cells in our laboratory had shown that the err subtype known as err is present in normal human prostate epithelial cells but exhibits reduced expression in many prostate cancer cell lines and clinical neoplastic prostate tissues

    中文大學解剖學系教授陳良教授解釋：過去我們在實驗室研究發現這種雌激素受體相關受體亞型（ err ）在正常人的前列腺上表達，但在一些前列腺癌細胞株和臨床前列腺腫瘤中err表達減少。
  11. On the other hand, inhibitory areas of ftc could be abolished partially or completely during bicuculline application. these results showed that gabaergic inhibitory afferent projections to recorded neurons were activated by random resonance caused by weak noise in cochlea, which provided inhibitory input for sharpening frequency tuning and made neuron more precisely analyze sound signal near its bf. therefore, this experiment presented a possible evidence of cellular level for interpreting why human and animal could extract or capture sound signal of specific frequency from the environment with competing noise

    說明山弱噪聲引起的耳蝸隨機共振在_ _仁行傳入過程中可能激活了至所一記錄的jc神經元的gaba能抑制性神經迴路，這種gaba能抑制為銳化神經元頻率調諧提供了一種抑制性輸入，使ic神經元對靠近最佳頻率的頻率分析變得更為細致和精確，由於聲頻率是聲信號的重要參數和信息載體，頻率調諧的銳化意味著對聲頻率分析能力增強，從而為解釋人們為什麼能從充滿噪聲的環境中捕捉或提取與行為學相關的信號提供了一種細胞水平的實驗證據。
  12. The study on the function and mechanism of phrip1 is important for clarifying how the cell plate and cell wall form in plants. in this study, full length of phrip1 is amplified by pcr and ligated into pks plasmid, then the bait plasmid, peg202 - phrip1, is constructed. the inseret gene are sure to be translated into the right fusion protein through its sequence. in the yeast two - hybrid system, the bait plasmid ( peg202 - phrip1 ) and a reporter plasmid ( psh18 - 34 ) are introduced into the yeast ( egy48 ) by co - transformation. then cdna library ( which is in pjg4 - 5 ) is screened and two genes are obtained. the two insert gene fragments are sequenced. one of them is plastocyanin, the other is putative photosystem i reaction center subunit ii precursor, both of them are the necessary components of photosynthetic chain

    成膜素相關蛋白1 （ phrip1 ）是一個含608個氨基酸的蛋白質，它對于植物胞質分裂中細胞板的形成起到了十分重要的作用。研究phrip1的功能和機制，對在分子水平上闡明植物細胞板以及細胞壁形成的機理具有重大的生物學意義。在本實驗中，根據phrip1的序列設計引物對其進行pcr擴增，得到該基因后將其連接到了pks質粒上，並進一步構建成了誘餌質粒peg202 - phrip1 。
  13. Carotenoids can make chla return from excited state to ground state by direct or un - direct quenching, in order to prevent algae from photooxidation. on the other hand, it was indicated that polysaccharides have functions in resisting uv. spirulina plalensis can accumulate both cellular and extracellular polysaccharides during uv treatment, it showed highest uv resistant ability ; nanochloropsis sp also can accumulate cellular polysaccharides, while extracellular polysaccharides reduced ; the cellular polysaccharides content of phaeocystis globosa scherffel decreased and extracellular polysaccharides content did not increased markedly, showing lowest uv resistant ability

    鈍頂螺旋藻和微綠球藻中在較低的uv輻射強度下類胡蘿卜素含量升高，而葉綠素a保持相對穩定，說明類胡蘿卜素可能對藻類起到一定保護作用，可能通過直接的或間接的方式猝滅激發態的葉綠素，來保障光合作用的進行；本實驗發現多糖的累積和分泌與藻體的抗uv能力有相關，鈍頂螺旋藻的細胞內和細胞外多糖分泌旺盛，其抗uv能力最強；微綠球藻體內能積累多糖，而胞外多糖分泌減少；球形棕囊藻的胞內多糖含量減少，胞外多糖含量增加也不明顯，其抗uv能力最弱。
  14. 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。
  15. Using km mouse as a animal model for studies on the maternal age effec t, we compared quantity, quality and in vitro developmental competence of oocytes from different age groups of mice to elucidate the possible mechanism of the decline in ageing - associated fertility

    本實驗以昆明白小鼠作為研究母體年齡效應的動物模型，比較了不同年齡段小鼠卵母細胞的數量、質量及體外發育能力等，以探討與衰老相關生育力下降的機制。
  16. From the view of cellular rheology, we examined the influence of fluid shear stress on the metabolism, morphology, structure and function of endothelia cells in our previous research. it is first time for us to develop the research between shear stress and apoptosis. in this study, we stimulate the human umbilical venous endothelial cells ( huvec ) by lps and apply different levels of fluid shear stress to them by a parallel plate flow chamber, then observe the change of apoptosis of endothelial cells by terminal deoxynucleotidyl transferase mediated dutp nick end labeling ( tunel )

    我們從細胞力學的角度，曾對血管內皮細胞在剪切力作用下的代謝、形態、結構及功能等進行過系統研究，但剪切力與內皮細胞凋亡的相關研究尚屬首次，我們希望通過探討細胞凋亡與剪切力大小及作用時間的關系，為探索剪切力對血管內皮細胞信號轉導的影響及作用機理提供有價值的參考數據和實驗資料。
  17. These suggest the bsp proteins and its homologous proteins are ubiquitous in mammals and must have some physical significances. in our research, to find and study the important role of bsp proteinsand their related proteins in the development of zygotes and to find the new gene related to bsp, we cloned a cdna gene sequence related to bsp proteins and make it express in eukaratic cells. the fusion protein acquired are purified are used to deduce its biological functions

    而在我們的實驗中為了發現和研究bsp及其相關蛋白在受精卵的發育中的重要作用，尋找bsp相關的新基因，克隆了一個與bsp蛋白相關基因的山一na序列並將該基因編碼的蛋白質在原核細胞中進行了表達和純化，將純化后的融合蛋白作了一些生物學功能方面的初步工作，發現新蛋白對tpk有一定的抑制作用，而tpk是細胞生長和代謝中十分重要的關鍵酶，這對于進一步研究新蛋白的生物學功能具有十分重要的意義。
  18. Other experiments revealed slight variatio in the size ， number ， arrangement ， and interco ection of the nerve cells ， but as far as ycho neural correlatio were concerned ， the obvious similarities of these se ory fields to each other seemed much more remarkable than any of the minute differences

    盡管其他實驗顯示在神經細胞的大孝數量、排列和相互連接上有一些小的差異，但是就心理-神經的關系而言，這些感官區域彼此之間的明顯的相似性看起來比起微小的差異更為令人注目。
  19. 15 heinrich r, neel b g, rapoport t a. mathematical models of protein kinase signal transduction. mol. cell, 2002, 9 : 957 - 970

    這些結果有助於設計相關的生物實驗，進一步研究細胞的jak - stat信號通路的對外界影響的變化。
  20. Methods ; rt - pcr method was used to amplify the coding sequence of sh2a gene. eukaryotic recombined expression vector, pcdnas. 1 - sh2a was constructed and then transfected bel7402 cell and cos

    細胞激酶活性測定相關試劑二、實驗方法通過rt pcr方法擴增shzacdna編碼序列，構建真核重組表達載體pcdna3
分享友人
分享到 Line

分享到臉書