鑒定染色 的英文怎麼說

中文拼音 [jiàndìngrǎnshǎi]
鑒定染色 英文
identification stain
  • 鑒 : Ⅰ名詞1 （鏡子 古代用銅製成） ancient bronze mirror2 （可以作為警戒或引為教訓的事） warning; objec...
  • 定 : Ⅰ形容詞1 （平靜; 穩定） calm; stable 2 （已經確定的; 不改變的） fixed; settled; established Ⅱ動詞...
  • 染 : Ⅰ動詞1 （用染料著色）dye 2 （感染） catch [contract] （a disease） 3 （沾染） acquire （a bad hab...
  • 色 : 色名詞[口語] （顏色） colour
  • 鑒定 : 1 （評語） appraisal （of a person s strong and weak points） 2 （評定） appraise; identify; auth...
  • 染色 : dye; dyeing; colouration; tintage; tinging; dyschroia; colouring; colour; [半] decoration染色不足...
  1. Identification of dyestuff classes on dyed textiles

    染色織物染料等級的鑒定
  2. 1. a new method to identify _ amylase activity and its producing bacteria : the blue complex was formed by unspecific adsorption, after mixing starch and trypan _ blue. the adsorption weakened when the starch was hydrolyzed to small molecular by _ amylase, and the trypan _ blue was released inside the hydrolyed zone. the starch around the zone which was not hydrolyzed adsorbed free trypan - blue so that the colour of medium became bluer than that of place in hydrolyzed zone

    快速鑒定並篩選-澱粉酶及其產生菌的新方法：錐蟲藍染料和澱粉由於靜電非特異性吸附結合后使澱粉呈穩定的藍色，當澱粉被澱粉酶水解后因分子變小吸附力減弱，而讓錐蟲藍游離出來，游離的錐蟲藍被周圍未水解的澱粉吸附而使顏色加深，澱粉水解區則形成無色、透明的水解圈。
  3. Conclusion ( 1 ) in our research, frequent expression of bsap in h / rs cell of classical hodgkin ' s disease provides further evidence for its b - cell origin, and the expression of bsap on h / rs cells also can be in favor of the identification of h / rs cells and can distinguish hl from alcl. ( 2 ) expression of bsap is located in nucleoli of cells, while that of cd20 in membrane

    結論（ 1 ）本研究在國內首次把bsap應用於hl的檢測，從蛋臼水平上為hl ； ts細胞的b細胞起源進一步提供了有力證據，升且有利於fiots細胞的辨認和與alcl鑒別； （ 2 ） bsap不同於cd20的細胞膜染色，它表達定位於核。
  4. This gene, artificially put under the control of camv 35s, was introduced into tobacco with the aid of agrobacterium, and the transgenic plants obtained were identified by gus staining, pcr and southern blot analysis

    將arge與組成型啟動子camv35s相連，構建植物表達載體，通過農桿菌介導轉化煙草。經過gus染色、 pcr及southern鑒定獲得了轉基因植株。
  5. Some of preblems will be accounted by means of stained thin section microscopic identification, catholuminescence microscopic observation, trace elent analysis, carbon and oxgen isotope geochemistry, and fluid inclusion analysis

    認為利用染色薄片鑒定、陰極發光顯微鏡觀察、微量元素分析、碳氧穩定同位素測定及包裹體測溫等綜合手段進一步研究，最終將解決這些問題。
  6. Primary culture of rat preadipocyte were prepared from the epididymal, inguinal and perirenal the fat pads of male normal, healthy, 15 - 20 days sprague - dawley rats. the preadipocyte grew better under the condition of 37, 95 % humidity, 5 % co2, ph 7. 0 - 7. 2, centrifuged at 1000r / min, m199medium, and 10 % fetal bo vine serum, seeded at a density of 4 l04, 5 l04, / cm2. oil red o staining was the special method to distinguish adipocyte from other cells, gimsa and he could determine the stage of the adiopcyte differentiation through the number of lipid drop, size and the position of the nucleolus of the staining fat cell

    經過多次實驗，確定本實驗室大鼠前體脂肪細胞的最佳培養條件是：溫度為37 ，濕度為95 ， co _ 2濃度為5 ， ph值為7 . 0 7 . 2 ，離心力為1000r / min ，培養基為m _ （ 199 ）培養基，胎牛血清濃度為10 ，合適細胞接種密度為4 10 ~ 4 、 5 10 ~ 4個/ cm ~ 2 ，染色結果表明：油紅o染色是鑒定脂肪細胞的特異方法， gimsa和he染色可根據不同區域染色程度、著色差別判斷細胞核的位置及脂滴大小、多少，觀察大鼠前體脂肪細胞分化過程中的形態變化，進而確定脂肪細胞的分化階段。
  7. Studies of genes related to heart development in drosophila contribute to reveal the mechanisms of human heart development and the congenital heart diseases. to clone and identify new genes that control the heart development, by a way of chemical mutagen, ems, we have established 1, 200 balanced - lethal lines on chromosome 2 and 3. with the screening the 330 stocks with immunochemical method using heart - specific antibody, mab. no. 3, we detected 60 lethal lines showing heart mutant phynotype

    為了克隆和鑒定控制心臟發育的新基因，本研究利用化學誘變劑甲磺酸乙酯大規模地誘變果蠅，並且建立了1200個第二和第三染色體的平衡致死系，利用心臟組織特異抗體mab . no . 3對其中330個品系進行免疫化學方法篩選，觀察到有60個致死系表現出心臟突變表型， 20個品系的心臟突變表型有待進一步證實。
  8. The first and second longest chromosomes are important in karyotype analysis and most of which are metacentric chromosome and submetacentric chromosome in lilium. hybrids were distinguishable by the existence and position of secondary constriction and arm ratio

    百合的第一對和第二對染色體多為中著絲粒和近中著絲粒染色體，可以根據次縊痕有無與位置及臂比鑒定雜種。
  9. The karyotypes often of them were analysed. the rapd fingerprints and systematics of thirty wild species including the fourteen wild species mentioned and two cultivars in the family were studied. these were intended to provide theoretical reference at the cytological and molecular lever for species identification, systematics study and breeding work of these plants

    本文對海南境內的14個野生種菊科植物進行了染色體計數，並對其中的10個種進行了核型分析，同時對包括上述14個種在內的30個野生種菊科植物和2個栽培種菊科植物進行了rapd指紋圖譜與系統學研究，旨在為這些植物的物種鑒定、系統學研究和育種工作提供細胞學水平、分子水平的理論依據。
  10. Methods of vegetable cell ploidy level identification

    蔬菜作物染色體倍性鑒定方法概述
  11. Methods of vegetable cell ploidy level identification were reviewed. their advantages and disadvantages were also discussed

    摘要綜述了蔬菜作物細胞染色體倍性鑒定的各種檢測方法，並對其優點進行了評述。
  12. Observation on chromosome numbers of 6 european pears

    6個西洋梨品種染色體數目鑒定
  13. According to the result showed at 280nm and at 490nm, in the comparison of whether protein absorption top and sugar quantity top overlapped, glycoproteins would be detected preparatorily, and as a result, tubes in two distinct areas had glycoproteins by this method. proteins were precipitated with trichloroaceticacid and with cold acetone, and glycoprotein was determined from sds - gel

    再從各收集管的收集液中，用三氯乙酸沉澱蛋白法、冷丙酮沉澱蛋白法相結合濃縮、制備蛋白樣品，進行sds ? page ，對sds膠進行pas糖鏈染色鑒定糖蛋白，並從茶樹葉分級蛋白中準確地鑒定出兩個區域的收集管中含有多種糖蛋白。
  14. In addition, it introduces the characteristics and identification methods of medicinal plants, and latest achievements obtained in chromosome doubling of medicinal plants in recent years

    此外，還介紹了多倍體藥用植物的特徵、鑒定方法以及近些年來藥用植物染色體加倍所取得的最新成果。
  15. Gemmological characteristics and identification of a kind of dyed red coral imitation

    一種染色紅珊瑚仿製品的寶石學特徵及鑒定
  16. Finally, a tranfer vector named as pltk - ha was constructed based on pltk - uni with insertion of ha gene of h3 subtype srv. the pltk - ha and prv bartha - k61 genomic dna were co - transfected into 50 - 70 % confluent vero cells in 6 - cm dishes. based on the expression of lacz gene, recombinant prv were selected and purified by blue - colored virus plaque

    利用脂質體介導的方法，將pltk - ha與prvbartha - k61基因組共轉染于亞單層vero細胞，依據報告基因lacz在細胞中的表達，篩選藍色蝕斑的重組病毒，經數次蝕斑純化后， pcr鑒定、 western - blot分析。
  17. The identified proteins are involved in a variety of cellular process including several zinc finger proteins relevant to transcription regulation, such as zinc finger 198, 263, 14, 224, zf6, novel protein similar to transcriptional represser ctcf, and kruppel - like zinc finger protein ; two members of the adams ( a disintegrin and metalloprotease domain ) family ; two members of integrin family ; several proteins involved in the signal transduction, cell - cycle control, chromatin remodeling and transcription repression ; and also some proteins of cell skeleton and some with unknown functions

    鑒定出的蛋白包括多個與轉錄調控相關的鋅指蛋白，如鋅指蛋白198 、 263 、 14 、 224 、 zf6 、轉錄抑制因子ctcf樣蛋白、幻肚pple樣鋅指蛋白等:兩個含金屬蛋白酶結構域和整合素結合結構域的家族成員adam28和adam17 ;兩個整合素家族成員pz整合素和含十個egf樣結構域的整合素（ tied ） ;與細胞信號轉導通路有關的蛋白;與細胞周期調控有關的蛋白;與染色體重塑和基因轉錄抑制有關的蛋白;細胞骨架蛋白以及其他功能未明的蛋白等。
  18. So this study will reveal the human expressions of hsp70, bfgf, cox2 after cerebral contusions and the relationship between the expression and the contusion time utilizing the immunohistochemical staining, at the same time, this study will find out the diversity between the autopsy case and the animal experiment, which can provide the theorical evidence to identify the aging cerebral contusion

    故本實驗採用實際工作中的案例標本，應用免疫組織化學染色，旨在了解人腦挫傷后hsp70 、 bfgf和cox2的表達，揭示其表達與人腦挫傷時間變化關系，同時觀察屍體解剖標本與動物實驗標本免疫組織化學的差別，為腦挫傷時間判定實際鑒定工作提供一條可行的理論依據。
  19. By using this method, multi - glycoproteins were detected from the tubes in two distinct areas. purification of glycoprotein using same condition of sds - page, same proteins were loaded, stained both with coomassie blue and with gel code glycoprotein staining kit respectively. under the condition, we successfully recovered glycoprotein bands from sds - gel by passive diffusion of proteins

    糖蛋白的純化選擇了相同樣品、相同的電泳條件，用考馬氏藍染色、糖蛋白試劑盒染色，分別對同一糖蛋白樣品對照鑒定，用蛋白質的被動擴散回收法，成功地從sds膠上快速地純化多種茶樹葉糖肽。
  20. Cells were collected after being passaged 5 times and used to identify infection by rt - pcr, direct fluorescent antibody, sandwich elisa. results indicated that integrated particles of csfv could be obtained from constructed full - length cdna

    連續傳代5代以後，收集各w摘要代細胞至第10代，採用rt一pcr 、直接熒光抗體染色和夾心elisa技術進行鑒定，結果均為陽性。
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