胞外域 的英文怎麼說

中文拼音 [bāowài]
胞外域 英文
extracellular domain
  • : 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...
  • : Ⅰ名詞1 (外面) outside; external side 2 (外國) foreign country 3 (以外) besides; beyond; in ...
  • : 名詞(在一定疆界內的地方; 疆域) land within certain boundaries; territory; region
  1. 1 sassler cn, bloomfield gl, fowler aa. current concepts of sepsis and acute lung injury. clinics in chest medicine 1996 ; 17 ( 2 ) : 213 - 235

    2潘芳,李文志.肺泡型上皮細的體培養及其在麻醉學研究領的應用.國醫學麻醉學與復甦分冊2000 ; 21 ( 6 ) 368 - 371
  2. His found that a large number of crystal cell is one of the typical salt - resistant characteristics in high - saltnity halophytes, and the distribution of salt hydronium inside plants appears obvious regional characteristic of many arrangements : salt - hydronium - - vacuole - - despersed singal crystal cell or vacuole bags which contain salts - - vacuole bags or crystal cell in groups or distributed as groups - - little consecutive crystal cell ring of organ periphery - - consecutive crystal cell ring of organ periphery

    發現大量的含晶細是高鹽度鹽生植物的一種代表性的抗鹽結構特徵,並且鹽離子在植物體內的分佈呈現出明顯的多層次性的區化特徵:鹽離子液泡分散的單個含晶細或含鹽液泡包成群或成堆分佈的含鹽液泡包或含晶細器官周不太連續的含晶細環器官周連續的含晶細環。
  3. It is interesting that pma plus calcium ionophore a23187 can inhibit pma - induced pta1 expression, and this effect ca n ' t be reversed by calcmeurin inhibiter fk506. pta1 mabs can inhibit ctl activation and differentiation in mixed lymphocyte culture system when added at the beginning of the culture but can induce platelet activation and aggregation in the fc dependent manner. in 1997, pta1 cdna was cloned from cdna library of tpa activated jurkat cells, which belongs to immunoglobulin superfamily ( igsf ) with two v - like domains of extracelluar region of pta1

    Il - 2 、 tnf - 、 pma可以使t細pta1表達上調, tgf -可以下調pta1的表達,而pma加上鈣離子載體a23187可以顯著抑制pma的上調作用,且這種抑制作用不被calcineurin抑制劑fk506所逆轉, 1997年burns教授從pma活化的jurkat細cdna文庫中克隆了pta1cdna全長,證實pta1是一個新分子,屬于免疫球蛋白超家族,區有兩個v樣結構
  4. To neutralize the function of cam, the cam binding domain peptide from bovine calcineurin a subunit was chosen because the pre - experiment demonstrated that bovine calcineurin could bind to calmodulin strongely in an acidic and high calcium concentration condition which is similar to the cell wall environment. in order to increase the binding ability of the chimeric secreted calmodulin binding peptide, the plasmid containing two copies of calmodulin binding domain were constructed

    它共有26個氨基酸,具有信號肽的典型特徵。為了削弱質體cam的功能,選擇了牛腦鈣調神經磷酸酶can ( calcineurin )的a亞基的cam結合。預實驗結果表明,在近似於環境的酸性高鈣條件下can與cam有強結合。
  5. Screening and constructional analysis of extracellular at the ligand binding domain of the vascular endothelial growth factor receptor flt

    配體結合的篩選及其結構分析
  6. The condition of profiles in outer station did n ' t change much in spring cruise, but showed more variable in near - shore stations when observed in different time. fluorescent characteristic per cell can be obtained by flowcytometric analysis. based on fluorescence data of synechococcus of all stations, two distinctly pigment - containing cell types coexisting can be found in some stations of east china sea, which located in all depth of p3, mixlayer of e7, 40 - meter depth of e6 of autumn cruise and in mixlayer of p2 of spring cruise

    通過對流式細計測量的細熒光結果來看,在秋季的p3 、 e7整個混合層、 e6站40米層,春季的p2站均發現有兩群不同色素含量的聚球藻( high一pe和low一pe )共存現象,極有可能分別屬于不同品系,春季共存站位位置比秋季時更靠,表明在秋季p3 、 e7等站位的共存是季節性現象,可能與此季節黑潮次表層水沿陸架坡涌升入侵到中陸架有關,水團的運動及混合使從海遷移而來的high一pe與近岸的low一pe得以共存,在春季,由於長江沖淡水的日漸強盛,在中陸架區的共存區有所移。
  7. Expression system renders products that are free of post - translational modifications, it is likely that the binding of crylab toxin to bt - r3 protein via protein - protein interaction and does not require glycosylation

    且該受體蛋白與cry1ab的結合部位位於bt - r3受體蛋白的結構。 bt毒蛋白與鈣粘蛋白受體的結合與受體是否糖基化無關。
  8. With the development of science and technology, the need of micro system is more and more urgent in many technical fields, such as various operation of cell and polymerized substances, micro surgery, scanning probe microscope ( spm ), butting optical fiber, fine manufacturing etc. with the development of micro - technology, micro mechanism, which has the character of micro size or micro motion is new high technology from microcosmic point of view understanding and reconstructing the world, micro mechanism technology is important means for researching nanotechnology, so the micro stereo vision ( msv ) techniques are demanded urgently in microcosmic domain

    隨著科學技術的發展,許多領越來越迫切地需要微型系統或微動系統,如生物細、聚合物的各種操作、微科手術、掃描探針顯微鏡spm 、光纖對接和微細加工等;而且隨著微技術的不斷發展,以形狀尺寸微小、操作尺度極小為特徵的微機械已成為人們從微觀角度認識和改造客觀世界的一種高新技術;微機械技術還有望成為研究納米技術的重要手段,因此在微觀領迫切要求顯微立體視覺技術的發展。
  9. 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( tmd )將它分為內和兩個部分,它的有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;它的內有1個整合蛋白( integrin )識別位點。
  10. 2. the functional of the purified trka extracellular domain proteins were tested using pc - 12 cells

    2 、用pc12細株測定腸ka膜各結構重組蛋白的功能。
  11. 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亞細定位研究,結果顯示:在白芷愈傷組織細和花序軸細中金顆粒主要分佈在細壁區,而在細內未發現或僅有少量金顆粒分佈,表明ecbp21蛋白主要定位於細壁區,這為細cambp ( ecbp21 )的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。
  12. “ when we looked at distance from the ship channel we find data that suggests there is an association with chemicals in the air and childhood leukemia, ” said ann coker, professor of epidemiology at the uniersity of texas school of public health in houston

    依照休斯頓城(其為此項研究提供資金)的聲明:這項研究發現,在船道的石油化工企業2英里之內的1 , 3 -丁二烯的濃度升高,居住在此區內的兒童急性淋巴細白血病其發病率比那些居住在10英里之的兒童增加了56 % 。
  13. We found that insulin - degrading enzyme ( ide ) interacts with ge through its extracellular domain

    我們發現胰島素降解酶( ide )可通過其細與糖蛋白e相互作用。
  14. Other domains of the extracellular part of bt - r3 protein are 11 cadherin repeated domains, which mainly consist of p stands that are linked by loop structure, turn residues and random coil

    其餘的形成以折疊為主的11個鈣粘蛋白重復結構。這些d折疊又由loop結構、轉角和無規捲曲連結在一起。
  15. The cadherin repeated domains of bt - r3 protein share high homology with the cadherin domains from african clawed frog ( xenopus laevis ) and e - cadherin ( epithelial ) from mouse ( mus musculus ). so, the 3rd structure of the cadherin repeated domains of bt - r3 protein should be similar to these domains

    Bt - r3受體蛋白的鈣粘蛋白結構分別與非洲爪蟾( xenopuslaevis )的鈣粘蛋白結構和小鼠( musmusculus )的上皮鈣粘蛋白結構有很高的同源性。
  16. In this review, recent advances in the cytopathology of gynecological tumors, ovarian borderline tumors, two types of endometrial cancer, vulvovaginal soft tissue tumors and the role of immunohistochemistry in the diagnosis of gynecological tumors are discussed

    摘要本文結合近年來婦科病理診斷領的新進展,從婦科細學、交界性腫瘤診斷進展、子宮內膜癌的分型、陰和陰道間葉源性腫瘤、免疫組化在婦科病理診斷中的應用等方面進行了綜述。
  17. Trka, the high affinity ngf receptor, contains an intracellular domain with tyrosine kinase activity and an extracellular domain with three tandem leucine - rich motifs flanked by two cysteine clusters in their amino termini and two immunoglobulin - like domains in the more membrane - proximal region

    含有8個亮氨酸的重復區,其前後分別串聯著一組半胱氨酸殘基,緊挨細膜的是兩個c2 -型免疫球蛋白樣區ig和ig ;膜內為酪氨酸激酶催化活性區。
  18. Sds - page proved that the molecular weight of expressed product of the extracellular part of bt - r3 was about 160kda. western blotting showed that the recombinant protein could specifically bind to bt toxic protein crylab, indicating that the bt - r3 is a receptor protein of crylab. the binding site of bt - r3 with crylab was located in extracellular domains of bt - r3 protein

    用大腸桿菌系統表達的bt - r3基因的結構的分子量約為160kda , western - blot實驗證實,重組蛋白能有效地結合bt毒蛋白cry1ab ,從而進一步確證了bt - r3是cry1ab的受體基因。
  19. Considering that aspartic acid ( d ) and glutamic acid ( e ) are very similar to each other, together with the biological function of the landmark, thus that the two landmarks can be regarded as no difference ; 3 ) conservative cysteine in terms of their numbers and positions in the extracellular domain. in ghr1 group, fghrl and zfghrl have seven cysteins, which are the same as that of quadruped. in ghr2 group which includes cohoghr isf1, cohoghr isf2, chghr, fghr2 and zfghr2, the cysteine number and positon are very similar to each other but are different from ghr1 group. especially, the fghr2 has five cysteins that is one more than zfghr2 ; 3 ) conservative boxl domain. with all the ghrs identified so far, boxl are comprised of ppxpxp ( x represents any amino acid )

    在fghri和zfghri都為7個,數目和四足動物ghr一致;在fghrz膚氨酸殘基為5個, zfghrz為4個,和同屬于ghrz的eohoghrisfl 、 eohoghrisfz 、 ehghr基本保持一致,但是卻和傳統的ghri有比較大的區別; 3 )本試驗克隆和分離得到ghri和ghrz以及所有目前發表的ghr都有比較保守的boxl結構,氨基酸組成為ppxpxp ,研究表明最後兩個脯氨酸殘基作用最大; 4 )在所有ghr中都完全一致的boxz ,序列為料efi ; 5 )在ghri和ghrz內部分都比較保守的酪氨酸殘基,他們被認為在信號傳導中起作用。
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