次生細胞 的英文怎麼說

中文拼音 [cìshēngxìbāo]
次生細胞 英文
secondary cell
  • 次 : Ⅰ名詞1 （次序; 等第） order; sequence 2 [書面語] （出外遠行時停留的處所） stopping place on a jou...
  • 生 : Ⅰ動詞1 （生育; 生殖） give birth to; bear 2 （出生） be born 3 （生長） grow 4 （生存; 活） live;...
  • 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...
  • 細胞 : cell; sytes; bioplast; cella; [口語] gene; [生物學] cellule; cellule cellulli cellulo ; cello ; k...
  1. Contains nutrition factors which are extracted repeatedly from herbs ( rcf ), adopts american technology, it will promete metabolism to reactivate your skin sell. it will activize and nourish skin, stimulate their regeneration process, prevent skin from ageing leave supple, whiten, smooth and ever - young complexion, used this product after seven times, you will have perfect skin

    引進美國技術，生物分化提取珍貴細胞再生因子（ rcf ） ，其獨特的活化細胞再生功能可加快皮膚的新陳代謝，充分的補足深層肌膚的營養及水份，深度美白肌膚，使皮膚水嫩透白，光滑，富有彈性，只需使用七次，即可重現動人光彩。
  2. The conditions promote the multiple formation of adventitious buds and regenerated roots in proliferating colonies of cells.

    環境促進滋生的細胞群落多次形成不定芽與再生根。
  3. Using cd, cu, zn and cr as experimental toxicants and crucian as experimental creature, we employed the environmental biotechniques ( flame atomic absorption spectrophotometry, the method of improved pyrogallol autoxidation and electron microscopy ) to study the acute toxicity and secure concentrations of heavy metals to crucian ; the accumulation and distribution of mixed heavy metals to fingling crucian ; the activities of superoxide dismutase ( sod ) of gill and liver tissues and the hispathological and ultrastructural change of superfine structure of liver and kidney of crucian after cadmium exposure. through which, we intended to fully and systemically study the toxic influence of heavy metals to fish, and preliminarily discuss the influence of heavy metals pollution to the diversified level of fish such as individual, organ, tissue, cell and molecule. thus we tried to provide scientific evidence to establish preventative management measures, avoid and relieve the harm of heavy metals pollution to aquicolous ecosystem in time

    隨后以這幾種重金屬作為實驗毒物，以鯽魚為實驗動物，應用環境生物技術、火焰原子吸收分光光度法、鄰苯三酚自氧化法、透射電鏡等技術研究了重金屬cu 、 zn 、 cd和cr對鯽魚的急性毒性及其安全濃度評價、混合重金屬在鯽魚幼體組織內的積累和分佈、 cd對鯽魚鰓和肝臟中sod活性的影響、 cd對鯽魚肝細胞和腎細胞超微結構的影響等，全面和系統地研究了水環境中重金屬暴露對魚類的毒性影響，初步探討了重金屬污染對魚類的個體? ?器官? ?組織? ?細胞? ?分子等各水平層次的影響，為制定漁業生產上預防性的管理措施提供科學依據，及時避免或減輕重金屬污染對水生生態系統造成的損害。
  4. Trial 2, effect of supplemental copper of different type on nutrition and specific immunity of mice - ii the grouping of trialt animal was the same as trial 1, at the first day, second day, third day, one mouse was injected with pha brine fluid for 10mg / kg avoirdupois after weighing in the same time in each repeat, following the 7d, 14d, 21d, 8d feeding period, after weighing, blood was made, wrigh - giemsa coloration, counting the number of lymphocyte female cell and overage lymphocyte, index of immune organ, copper concentration in liver and spleen

    試驗二，不同形式銅對小鼠營養與特異性免疫功能的作用-試驗動物分組同試驗一，進入正式試驗期后，在每周第1天、 2天、 3天同一時間每重復選取1隻小鼠，稱重后每天按10mg kg體重肌肉注射一次植物血凝素生理鹽水溶液，並於試驗第7天、 14天、 21天、 28天稱重后尾尖取血，姬姆薩-瑞氏染色，計算t淋巴細胞轉化率，計算免疫器官指數，測定肝臟、脾臟銅含量。
  5. The primary results showed : using m199 as diluents containing 20 % bovine serum, it is better to freeze the cells slowly freezing at fist then increase freezing speed ( for example, from 0 to - 6 freezing speed is about - 0. 05 a minute, from - 6 to - 40, freezing speed is about - 0. 5 a minute ), studies on effect of various concentration of dmso demonstrate that about 12. 5 % dmso gave the highest post - thaw percentage of viable cells. the concentration of bovine serum had no different effect on the percentage of the viable embryo cells of misgurnus auguillicaudatus. the embryo cells derived 6 from the later stage of blastula offish is more resistant to the cryogen than the cells of early stage of blastula. the cells preserved in liquid nitrogen at - 196 were thawed and cultivated, a few cells were found adhere to the surface of culture vessel when the percentage of viable cell was more than 30 %. the cells in only two culture vessels were found to proliferated and gave rise to many small morphologically undifferentiated cells

    研究初步表明:以細胞培養液m199 （含2既的小牛血清，常規量雙抗）為凍存稀釋液對泥鰍胚胎細胞冷凍保存宜採取先慢后快的方式（例如，從0一一6 ，凍存速度為一0 . 05 / min ，再以一0 . 5 / min的速度從一6一一40 ） ; dmso的保護效應濃度為12 . 506左右;小牛血清的濃度對泥鰍胚胎細胞的成活率影響不明顯;囊胚晚期細胞抗凍性比中早期強;通過對不同批次的凍存細胞解凍培養，解凍后成活率為30 %以上細胞培養數天後均有少數細胞貼壁，但只發現兩瓶培養細胞有明顯增殖現象產生許多未分化的小細胞。
  6. In trpsin tolerance assay. this virus could resist to 1 % trpsis at 37 in an hour. in acid tolerance assay, this virus was resistant to ph3. 0 and ph5. 0 at 37 in 2 hours, and the average infection litre of the virus decreased little. in heat assay, at 50, the virus was processed from 5 minutes to 150 minutes and at each condition the viral virulence reduced to some certain degree. among these conditions, when at 50 in 30 minutes. the average infection litre of this virus decreased over 2 tilre. and when al 50 in an hour, cpe of ihis virus disappeared. when time was set for an hour. but with processed in different temperature as 50 60 70, 80, the virus losl the multiplication capacity complelely. in biological assay, we selected different cell lines to cultivate this virus by laking advantage of possesional cells at that time in our laboratory. then we found that fcwf cell line was the most sensitive to dxmv and mdck was the second. with f81 cell line, after passaged for 12 times continuously with low concentration of fcs. the virus could produce cpe. however, with vero cell line. the virus could not procuce any cpe after many passages. the hemagglutination and lumadsorption reaction test proved that this virus had no any reaction to erythrocyte of pig, fowl and cavy. by neutrolizaion assay, dxmv could be identified as a kind of ccv

    理化學研究表明，該病毒為rna病毒，對氯仿、乙醚敏感；胰酶試驗中，經37 、 1小時處理的病毒，仍然能夠在貓源細胞fcwf細胞上生長，並且毒力基本保持不變；耐酸性試驗中，病毒分別在ph5 . 0和ph3 . 0經37作用2小時，毒力僅下降一個滴度；耐熱性試驗中，該病毒在恆定溫度50 ，設定不同時間，從5分鐘到150分鐘，毒力均有不同程度下降，其中， 50作用30分鐘，病毒平均滴度下降2個單位； 50 ， 60分鐘， cpe消失；恆定時間1小時，設定不同溫度（ 50 - 60 - 70 - 80 ） ，病毒在細胞上完全喪失增殖能力， cpe消失。生物學試驗，利用實驗室現有條件，選擇不同的細胞系對該病毒進行培養，發現該病毒對貓源細胞fcwf最敏感； mdck細胞次之； f81細胞經多次傳代，亦可出現cpe ；而vero細胞則不敏感。血凝試驗表明，該病毒對豬、雞、人及豚鼠的紅細胞均無血凝性。
  7. Many of the cellular biosynthetic pathways were first elucidated.

    首次闡明了許多細胞內生物合成的途徑。
  8. Each second vibrates 3000000 times of slight massages, can thoroughly reach derma layer, warms up the effect can penetrate hypodermic, has the exchange of gases movement, the shallow layer cell repair ability strengthens, scarfskin layer ‘ s water fat membrane and the flesh resistance, guarantees the wet promotion, the flesh beautiful and moving

    萬次的細微按摩，能深入達真皮層，溫熱效果能深入皮下，產生氣體交換動作，淺層細胞之修護能力增強，表皮層之水脂膜與肌膚對外界之抵抗力、保濕提升，肌膚明媚動人。
  9. We have observed the following characteristics of anatomical structure and development : ( 1 ) the primary roots belong to archetype and the lateral roots occur in the position toward the xylem of the vascular cylinder ; ( 2 ) the root endodermis consists of thicken casparian strips, and there are from two lo four layers parenchyma cells near the pericycle ; ( 3 ) the pith and resins canals are absent in the toots ; ( 4 ) secondary structure occurs in the root hair zone, and vascular cambium is formed from the parenchyma cells between the primary xylem and primary phloem ; ( 5 ) tanning materials are abundant in pericycle cells and phelloderm cells ; ( 6 ) sclereids are found in secondary phloem, and rays are rather rich in secondary xylem

    結果表明：氣生不定根具有以下結構特徵和發育特點： （ 1 ）根為二原型，側根正對著木質部發生； （ 2 ）幼根內皮層細胞具凱氏帶加厚，維管柱內緊挨中柱鞘內側具有2 ~ 4層大型薄壁細胞； （ 2 ）根中無髓和樹脂道； （ 4 ）次生結構發生於根毛區，維管形成層由初生木質部和初生韌皮部之間的薄壁細胞轉化形成； （ 5 ）中柱鞘和栓內層細胞富含單寧類物質； （ 6 ）次生韌皮部有石細胞，次生木質部射線發達。
  10. In the present paper, some investigations on loxoblemmus doenitzi ( gryllidae ) are reported. in order to discover the meiosis of spermatomeres and spermiogenesis, slice - pressing method and improved phenol - fuchsin dyeing method are used. in the course of meiosis, primary spermatocytes directly enter metaphase ii, not through telophase i and prophase ii

    本論文以直翅目、螽斯亞目、蟋蟀總科、蟋蟀科的多伊棺頭蟋（ loxoblemmusdoenitzi ）為材料，採用壓片法-改良苯酚品紅染色，研究了精子發生過程中的減數分裂階段和精子形成，發現初級精母細胞第一次減數分裂后不經過末期和前期直接進入中期。
  11. During male gametogenesis, the spermatogonia became primary spermatozoa through mitosis, and then became fourth equivalent cytoplasm, round sperm through meiosis. after maturation, they participated in embryo development with the mature oocyte through fertilization. but in female gametogenesis, the primary oocyte formed a matured egg and 1 ~ 3 polar bodies ( pb )

    雄性動物精子發生過程中精原細胞最後一次有絲分裂形成二倍體精母細胞后，經過兩次減數分裂形成了四個含等量細胞質、圓形的精子細胞，最終發育成四個具有正常生理功能的精子，與成熟卵母細胞受精后參與胚胎發育。
  12. 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

    發現大量的含晶細胞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域化特徵：鹽離子液泡分散的單個含晶細胞或含鹽液泡包成群或成堆分佈的含鹽液泡包或含晶細胞器官外周不太連續的含晶細胞環器官外周連續的含晶細胞環。
  13. 2 - e4 and s2 is induced respectively by 8 - ag and 5 - brdu with different drug concentration to make them deficient in hypoxanthine - guanine phosphoribosyl transferase ( hgprt ) and in thymidine kinase ( tk ) respectively and renamed 2 - e4 - a and 82 - 6. their antibodies " isotypes are tested by goad anti - mouse isotype regent

    取馴化好並處于對數生長期的2 - e _ 4 - a和s _ 2 - b細胞，再常規融合和篩選，三次克隆化后得穩定分泌雙特異性抗體的雜交-雜交瘤細胞株6株。
  14. Abstract : the early embryo developmental block is a common phenomenon in mammal when embryos are cultured in vitro. many studies of phosphorus, glucose, hypoxanthine and cytoplasmic factors on early embryo developmental block carried out by different methods such as morphology, biochemistry, molecular biology and micromanipulation have been reviewed. the merit and shortcoming were analyzed and the necessity of using simple or components limited media overcoming early embryo developmental block were also reviewed. media that have been shown effective in overcoming early embryo developmental block in mouse, rat, hamster, rabbit, pig, sheep, cattle and monkey were listed

    摘要哺乳動物胚胎在體外培養中普遍存在早期發育阻滯的現象.對此，人們用形態學、生物化學、分子生物學、顯微操作等手段開展了磷酸、葡萄糖、次黃嘌呤和細胞質因素對早期胚胎發育阻滯的影響的研究.本文綜合分析了共培養系統的優缺點.說明了採用完全成分已知的培養液對進行有關研究的必要性.列出了有效運用於克服小鼠、大鼠、倉鼠、兔、豬、羊、牛、猴等動物早期胚胎阻滯的成分已知的培養液的名稱。
  15. Effects of infrasound on biological characteristics of osteoblast - like cells

    次聲波對成骨樣細胞生物學特性的影響
  16. We synthetically discussed intraspecific differentiation and evolution, from four biotic levels of population, individual, cell and gene. intraspecific differentiations in morphology were investigated firstly. the results indicated that there are varied polymorphsim within populations, and obvious polytypism among populations

    本文在形態分類的基礎上，根據居群生物學的原理和方法，對淡黃花百合的形態學、細胞學、分子生物學進行了研究，從居群、個體、細胞和基因四個層次綜合探討了該種植物的種內分化與進化。
  17. Secondly, scientists are trying to give the healing process an artificial boost by implanting " scaffolds " pieces of stretchy fabric that guide the orderly growth of new, healthy cells

    其次，科學家嘗試以外力協助復原過程，藉著植入由數塊伸縮性布料構成的支架，引導健康的新生細胞循序生長。
  18. In this report, we mainly covered the following aspects of " tissue organ regeneration and replication in situ " : 1 ) procedures of tissue organd regeneration and replication and replication in clnical practice ; 2 ) the discover and existence of potentiald regenerative cell ( prc ) ; 3 ) the proliferation, differentiation and regeneration law of potential law of potential regenerative cells ; 4 ) study procedure on tissue organ regeneration and replication from prcs in vitro based on the model of full skin organ regeneration in situ after extensive in vitro, set up the method and technology of searching life regenerative substance required in tissue organ regeneration and replication in situ. in this study, first, the whole human body is divided into 206 function units, which are the " tissue organ " in regeneration study. then the histology foundation of tissue organ regeneration and replication in situ is set up. in ordre to prove the existence of the potential regenerative cells and their potential baility and function, we established clinical tracking rechnique of skin organ regeneration in situ ; meanwhile, several tissue organ regeneration and replication in vitro models which represent different kinds of runctions were sucessfully set up, with all these techniques and models, we confirmed : 1 ) the existence, function and ability of pptemtoa regenerative cells ; 2 ) the importance of life regenerative substance ; 3 ) the feasibility of tissue organ regeneration and replication in situ ; 4 ) the big value of tissue organ regeneration and replication in situ in life science and medicine progerss. we also showed the possible foreground of capture cancer with this method and technologh. in this report, nearly 200 photographs of several tissue organ regeneration and replication in situ or in vitro demonstrated the whole process of tissue organ and big organ entities regeneration and replication from cells. the results of tissue organ regeneration and replication in situ mainly include : 1 ) whole skin organ regeneration and replication in situ ; 2 ) gastrointestinal mucosa tissue organ regeneration in vitro ; 3 ) hair follicle tissue organ regeneration in situ or in vitro ; 4 ) never tissue organ regeneration in situ ; 5 ) pancreas tissue organ regeneration and replication in vitro ; 5 ) marrow tissue regeneration in vitro ; 6 ) renal glomerulus and tubule tissue organ tugeneraation in vitro ; 7 ) heart muscle regeneration in vitro, etcl. in order to let more and more people know and understand this technology of tissue organd regeneration and replication in situ, herein, for the first time, we publicize the key points of actualizing this technology. also, we publicized the technology procedures and the frame constitute of life substances. we bilieve this is a big contribution to human science

    本研究報告，重點報道了組織器官的原位再生復制的臨床程序，報道了組織潛能再生細胞的發現和存在，以及該細胞的增殖分化和形成組織器官的變化規律.以燒傷后皮膚組織器官的原位再生復制為模型，研究出了體外組織潛能再生細胞復制組織器官的培養方法;以體外組織器官的復制為模型，建立了尋找原位組織器官再生復制所需生命物質的方法和技術.本研究，首先按人體的器官功能，分解為206個功能單位，確立了所復制的人體器官中的組織功能單位為組織器官，從而建立了原位組織器官再生復制的組織學基礎.為了驗證組織潛能再生細胞的再生潛能，建立了皮膚器官原位再生的實體臨床跟蹤技術，同時又建立了能代表有關器官功能類別的代表組織器官的原位和體外復制模型，以多組織器官的成功復制確定潛能再生細胞的作用，確定生命研究再生物質的重要性，確定組織器官原位再生復制的可行性，確定了組織器官原位再生復制的生命科學研究和醫學進步的重大應用價值，同時展示了用此方法和技術攻克癌癥的前景.本研究報告，以近二百幅多個組織器官原位和體外再生復制的實體圖片，展示了潛能再生細胞復制的組織器官和大器官司實體;展示了細胞再生復制器官的全過程.真實的報告了組織器官原位再生復制的成果.所公布的主要成果為:皮膚器官的原位再生復制;胃腸黏膜組織器官的原位和體外再生復制;毛囊組織器官的原位和體外再生復制;神經組織器官的原位復制;胰腺組織器官的體外復制;骨髓組織的體外復制;腎小球小管組織器官的體外復制;心肌的體外復制等.為了讓更多的人學會和掌握組織器官原位再生復制技術，本報告首次公布實施技術的重要環節和技術流程;首次公布了生命再生物質的框架和組成.作者自費研究成果對人類生命科學的一大貢獻
  19. In the first large - scale screen of genetic changes in cancer cells, researchers have found that a typical breast or colorectal tumor results from mutations in about 90 genes, with different sets of mutations producing the same type of cancer

    在首次癌細胞遺傳改變的大規模篩選中，研究者發現典型乳腺或者結直腸腫瘤源於約90種基因突變，不同的突變組合產生同種類型的癌癥。
  20. In this review, the present status of the molecular and physiological mechanism of the differentiation and development of cotton fiber is discussed, in which the molecular and physiological mechanism of the producing of the cell turgor, loosening of the cell wall, synthesis of the composition molecules and their incorporation into cell wall, signal of the starting of secondary wall thickening, cellulose biosynthesis, and layout of cellulose microfibril regulated by cytoskeleton are introduced in detail

    摘要本文綜述了棉纖維分化、發育的分子生理機制的研究現狀，著重討論了棉纖維細胞膨壓的產生、細胞壁的鬆弛、結構分子的合成和加入、次生壁增厚的啟始信號、纖維素的生物合成和細胞骨架系統控制纖維素沉積等機制。
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