胞內區 的英文怎麼說

中文拼音 [bāonèiqū]
胞內區 英文
intracellular region
  • 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...
  • 內 : 名詞1. （內部; 里頭; 里邊） inner; inside; within 2. （妻子或妻子的親屬） one's wife or her relatives 3. （姓氏） a surname
  • 區 : 區名詞（姓氏） a surname
  1. However, the advance of intracellular labeling techniques enables us not only to visualize more complete dendritic arbor for qualitative analysis, but also to examine the relation between changes in the dendritic arborization and the evoked fast postsynaptic curents - 3 - ( fpscs ) in the same neurons during the postnatal development the aim of this study was to systematically examine the postnatal changes in the configuration of fpscs evoked by the focal stimulation of the stratum radiatum of the ca1 region, and the relationship between the dendritic arborization and evoked fpscs in the rat hippocampal ca1 pyramidal neurons using whole - cell blind patch recording technique combined with biocytin intracellular labeling during the postnatal development ( postnatal day 2 - 70, p2 - p70 )

    但是，細胞內染色技術的進步使我們不僅能觀察到更完整的樹突分支來用於定性研究，而且也可以在同一神經元上研究在發育過程中樹突分支的變化與誘發的快突觸后電流（ fastpostsynapticcurrents ， fpscs ）之間的關系。因此，本研究應用盲法腦片膜片鉗記錄並結合biocytin細胞內染色方法，對發育過程中（生后2 70天）局部刺激大鼠海馬ca1區輻射層在錐體神經元誘發的fpscs的成分變化，以及ca1錐體神經元的樹突分支與誘發的fpscs的關系進行了較為系統的研究。
  2. Notch interaction with its ligands induces the cleavage of its intracellular domain ( ic ), and the notch ic translocates to the nucleus and binds to rbp - j, the mammalian homolog of su ( h ), to transactivate transcription of target genes such as e ( spl ) ( enhancer of split ), hesl ( hairy and enhancer of split ) and hes5 four notch receptors and their ligands are differentially and redundantly expressed in a variety of vertebrate tissues

    它通過其識別序列（ cogtgggaa ）結合於受調控基因的啟動子區，在轉錄激活因子的驅動下調節細胞分化和個體發育相關基因的表達。在沒有n 。 tch胞內段的情況下， rbpj可與包含sm盯（ silencingmediatorforretlnoldandthyroidhormonereceptor ）和組蛋白去乙酞化酶的轉錄輔助抑制復合物結合，當notch信號被激活時； rbpj可與n 。
  3. Inspection for the biological activities of recombination protein of ? ctla4 extracellular domain in vitro : we investigated the role of ctla4e in t cell proliferation of mlr with 3h - tdr incorporation

    重組人ctla4胞外區蛋白體內生物學活性研究： l ）觀察ctla4胞外區蛋白在小鼠變應性鼻炎中的作用。
  4. We used four different wavelength light including red light ( 750nm ), yellow light ( 580nm ), green light ( 560nm ), blue light ( 400nm ) to stimulate four different groups compound eyes. then the ultrastructures of the compound eyes of each group were observed under electron microscope. the results showed the fine structure of the photoreceptor, the diameter of rhabdom, the dimension of perirhabdom vacuole, the number of pinocytotic vesicle below the microsvilli, the location of pigment granules, the emergence of lamellar bodies and lysosomes in cytoplasm, were different in different light adaptation

    二、不同光照條件下復眼超微結構的變化三疣梭子蟹經過12h暗適應后，在不同波長的紅光（ 750nm ） ，黃光（ 580nm ） ，綠光（ 560nm ） ，藍光（ 400nm ）照射下，其光感受器的小網膜細胞和感桿束的形態和超微結構呈現較大的區別，感桿束的形態、細胞內的胞器隨不同波長光的適應而發生變化，在紅光下感桿束直徑最大，微絨毛排列整齊，在藍光下感桿束直徑最小，微絨毛最凌亂。
  5. Plants are thought to remove na + from the cytoplasm by transporting it into the vacuolar or out of the cell using na + / h + exchangers localized in the vacuolar and plasma membranes, respectively. sos1 encoding a plasma membrane na + / h + antiporter and atnhxl encoding a vacuolar na + / h + antiporter were isolated from glycophytic arabidopsis thaliana, and overexpression of atnhxl and sos1 in arabidopsis thaliana increased the salt tolerance of transgenic plants significantly

    目前，擬南芥細胞內控制na ~ +外排的基因sos1及離子區隔化基因atnhx1均已克隆， sos1及atnhx1在擬南芥中的過量表達顯著提高了轉基因植株的耐鹽性，開創了降低na ~ +毒害的基因操作新途徑。
  6. One is the accumulation of the solute osmo - protectants, the other is the mechanisms of ion homeostasis including na + extrusion system and na + compartmentation into the vacuolar to reduce the toxic effects of this cation

    一方面增加細胞內可溶性物質，另一方面則通過na ~ +外排或na ~ +區隔化機制來維持胞質內較低的na ~ +濃度，以消除na ~ +的毒害。
  7. It is divided to extracellular and intracellular part by transmembrane domain. there are 13 n - glycosylation sites, 20 protein kinase c phosphorylation sites, 28 casein kinase ii phosphorylation sites, 4 tyrosine kinase phosphorylation sites and 15 n - myristoylation sites in the extracellular part of bt - r3 protein. an integrin recognition sequences rod lies in intracellular part of bt - r3 protein

    跨膜區域（ tmd ）將它分為胞內和胞外兩個部分，它的胞外有13個潛在的糖基化位點， 20個蛋白激酶c的磷酸化位點， 28個酪蛋白激酶的磷酸化位點， 4個酪氨酸酶的磷酸化位點， 15個豆蔻（十四烷基）酰化位點；它的胞內有1個整合蛋白（ integrin ）識別位點。
  8. Resent studies demonstrate that, such as gabaar1 subunit of gaba receptor, ka2 and glur6 subunit of ka receptor, there are some functional regions in that of c terminus which can regulate these subunits targeting to the cell membrane surface. while little was known whether nmda receptor ' s nr2b subunit has the similar domains

    最近有一些研究報道，許多突觸受體如gaba （ b ）受體rl亞單位、 ka受體的kaz和glur6亞單位以及孤兒受體腿亞單位的胞內區，存在有影響受體運輸到細胞膜的功能區，但是尚未有對于nmda受體的nrz亞單位膜運輸的報道。
  9. Then using ecbp21 antibody and immunogold transmission electron microscopy method, we studied the subcellular localization of ecbp21. the results indicated that the gold particles were mainly localized in the cell wall in callus cells and rachis cells of angelica dahurica. these results indicated that ecbp21 mainly localized in cell wall, which provide a direct evidence of the extracellular existence of ecbp21. furthermore, using ecbp21 antibody and immunohistochemical method, we studied the organic specially distribution of ecbp21, the results indicated that ecbp21 distributed in all organize, but it distributed more in leave n flower rachis than in leafstalk and root

    首先，構建了ecbp21表達載體，誘導了重組蛋白的表達，並通過膠回收法獲得了大量純化重組ecbp21蛋白，制備了高效價、高特異性抗體；隨后，利用ecbp21抗體，結合免疫膠體金電鏡定位技術進行了ecbp21亞細胞定位研究，結果顯示：在白芷愈傷組織細胞和花序軸細胞中金顆粒主要分佈在細胞壁區域，而在細胞內未發現或僅有少量金顆粒分佈，表明ecbp21蛋白主要定位於細胞壁區域，這為細胞外cambp （ ecbp21 ）的胞外存在提供了直接證據：進一步，利用ecbp21抗體，通過免疫組織化學分析研究了ecbp21組織特異性分佈狀況，結果表明ecbp21在白芷各組織中均有分佈，但在葉、花、花序軸中分佈較多，而在葉柄、根中分佈較少。
  10. Rising computer power has recently enabled wireless devices operating in these upper bands to offer gigabits per second of instantaneous bandwidth within very small areas, or “ picocells, ” of coverage

    電腦運算效能提高，也讓無線裝置可在這些較高的頻帶運作，在非常小的區域（即所謂的微微細胞）內，提供每秒數十億位元的短時間頻寬。
  11. The nr2b subunit have a long cytoplasmic tail ( 644aa ), so it predicts that there may be some functional domains in this tail

    Nrzb含有很長的胞內區（ 644個氨基酸） ，推測它們很可能存在許多重要的功能區和調節位點。
  12. A change in functional properties of the nmda receptors has been invoked as a potential mechanism contributing to the loss of synaptic plasticity during brain maturation. from this, it is important to well understand the structural and functional diversity of nmda receptors in relation to nmda receptor subunit composition and spatial distribution at excitatory synaptic sites during development

    近幾年來，在哺乳動物中樞神經系統中，對離子型谷氨酸受體如何定位到興浙江大學醫學院碩士論文nrzb亞單位的c末端胞內區影響n協da受體裝配、運鈞以及表面表達的分子機制奮性突觸的研究有了長足的發展。
  13. In the relatively high dislocation density areas, dislocations form the relatively small cellular structure and there is few isolated dislocation within each cellular structure. here the profile of c concentration in the dimension of a cellular structure is " u " - shaped. the cell diameter increases as the dislocation density decreases, dislocations form the relatively large cellular structure and there are a few isolated dislocations within each cellular structure

    發現晶片中位錯密度和分佈嚴重影響碳的微區分佈，高密度位錯區，位錯形成較小的胞狀結構，胞內無孤立位錯，碳在單個胞內呈u型分佈；較低密度位錯區，胞狀結構直徑較大，胞內存在孤立位錯，碳在單個胞內呈w型分佈。
  14. Ngf binding to trka receptors results in receptor dimerization and kinase activation. recent evidence supports that not all extracellular subdomains are responsible for receptor activation. structure based drug design for neurotrophic agonists with small molecular weight relies on knowledge of the interaction of neurotrophin with their receptors

    Trka在ngf作用下發生二聚化，使胞內域中酪氨酸激酶區激活，從而使trka中酪氨酸自磷酸化，並進一步激活胞內信號轉導通路，從而實現神經營養信號傳遞。
  15. The cdna of hn gene from b95 strain, shares a high identity between 88 % and 95. 1 % with that of reported hn genes. the amino acid residues predicted, shares an identity between 92. 1 % and 96. 1 % with that of other strains

    1 ，氨基酸的差異主要集中在n端18 75位。該范圍內包括hn蛋白胞質區、跨膜區和細胞外區。這些變異對hn蛋白生物活性的影響還有待進一步研究。
  16. The intracellular domain has four distinct regions : the ram domain, the ankyrin repeats, a transcriptional activator domain ( tad ) and the pest ( proline -, glutamate -, serine -, threonine - rich ) sequence. two nuclear localisation sequences are present prior to and following the ankyrin repeats

    釋放的胞內區不經其它信號轉導分子的作用可直接進核，與dna結合蛋白rbp - j相互作用並激活下游基因如果蠅的e （ spl ） （ enhancerofsplit ）復合體及哺乳類的hes （ hairyandenhancerofsplit ）家族基因。
  17. Kyot2 lacked two lim domains from the c terminus and had a frameshift in the last exon, creating the rbp - j - binding region in the c terminus. kyotl had a negligible level of interaction with rbp - j. the binding site of kyot2 on rbp - j overlaps those of ramic and kyot2 repressed the rbp - j mediated transcriptional activation by ramic by competing with them for binding to rbp - j

    在肌肉母細胞系czc12內過表達kyoth時可阻斷轉錄激活物notch胞內區或ebnaz對rbp依賴性啟動子的轉錄激活作用，這種阻斷作用呈劑量依賴性，提示kyoth可與notch胞內區或ebnaz競爭rbp j上的結合位點，從而抑制二者的轉錄激活活性
  18. In order to get some functional clues from their structures, the upstream regulation region of ndrgl gene and second structure of ndrg2 protein are performed bioinformatics analysis ; we found that there are several binding sequences of some diffirent transcription factors, their functions include regulating tissue - specific gene expression, regulating expression of genes related to growth and early development of cells, besides this, regulating expression of genes under some stimulated conditions, and so on. predict in protein fold classification shows that ndrg2 belongs to alpha / beta hydrolase fold family, and there are high similarity between ndrg2 and epoxide hydrolase from bacteria, this suggests that ndrg2 protein may has enzymatic functions associated with resisting the oxidative stress, maintaining the balance of cell redox potential, involving in the metabolism process of xenobiotics or intracellular toxic molecules

    研究發現呷基因的調控區存在多種轉錄因子結合位點，功能主要涉及組織特異性表達調控，細胞生長發育相關基因的表達調控，刺激反應基因的表達調控等； ndrgz蛋白在結構上屬于a小水解酶類折疊，折疊分類預測表明ndrg2與其中的的細菌環氧化物水解酶的二級結構極為相似，提示ndrgz蛋白具有一定酶活性，可能參與細胞抗氧化應激反應，維持細， an ） armtbffiofbfochmilsyn ） mdafblechmrbfobo4第四軍醫大學碩士學位論文胞內氧還電勢平衡，參與內外源有毒物質的代謝等。
  19. [ methods ] by using the overall rna of our previously cultured human melanoma cell line ( a375 ), full length fasl gene is detected by rt - pcr. using the cdna as template, . the extracellular domain of fasl ( fasl - ecd, 127 - 278aa ) is amplified by pcr. the pcr products are directly cloned into t vector pmd - 18t

    L方法採用新鮮人黑色素瘤細胞（ a375 ） ，抽提該細胞的總rna ，進行rt一pcr反應分析a375內fasl全長編碼基因的轉錄表達，以a375細胞cdna為模板，用pcr產物直接克隆法擴增人fasl一ecd （人fasl胞外區）的編碼基因，即127一278位氨基酸殘基，而後將pcr產物直接克隆于pmd一1st載體中，獲得重組質粒pmd一t - fasl一ecd ，進行dna測序。
  20. We concluded that excessive expression of exogenous htr gene may compete with the endogenous telomerase rna and prevent rna template from combining with telomeric dna, thus repressing the elongation of telomeric dna ( telomeres ) and causing cell aging and cell death. - 6 - 3. some modifications have been made to overcome the limitation of conventional telomeric repeat amplification protocol ( trap ) assay

    分析其原因，可能是htr基因的過表達在數量和空間效應上同細胞內的端粒酶rna組分產生竟爭，一定程度上阻礙了端粒酶rna模板區與端粒dna的結合，從而抑制端粒dna的延伸，導致細胞凋亡。
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