白細胞顆粒 的英文怎麼說

中文拼音 [báixìbāokēlì]
白細胞顆粒 英文
leukocyte granule
  • 白 : Ⅰ形容詞1 （似雪的顏色） white 2 （清楚; 明白; 弄明白） clear 3 （空的; 沒加他物的） pure; clear; ...
  • 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...
  • 粒 : Ⅰ名 （小圓珠形或小碎塊形物） small particles; grain; granule; pellet Ⅱ量詞（用於粒狀物）
  • 細胞 : cell; sytes; bioplast; cella; [口語] gene; [生物學] cellule; cellule cellulli cellulo ; cello ; k...
  • 顆粒 : 1 （小而圓的東西） pellet; bead; dust; anything small and roundish （as a bean pearl etc ）2 （一...
  1. Expanded bed adsorption ( eba ) is a novel bioseparation technique, which integrates clarification, concentration and initial purification into a single unit operation. it enables proteins to be recovered directly from unclarified cultivations of microorganisms or cells and homogenates of disrupted cells, without the need for prior removal of suspended solids. matrix is the principal " hardware " pillar supporting the successful application of eba

    擴張床吸附（ eba ）技術是一種新型的生化分離技術，它集成了固液分離、濃縮和初期純化於一步單元操作之中，可以直接從含有細胞和細胞碎片的發酵液或培養液中提取目標蛋白，而不必事先除去懸浮的固體顆粒。
  2. Effect of shuanghuang shengbai granule on radiotherapy or chemotherapy induced leukopenia in mice

    雙黃升白顆粒劑對小鼠白細胞減少癥的影響
  3. By sds - page and immuno - blotting, we found that a monoclonal antibody of anti - chick brain cytoplasmic dynein intermediate chain antibody could react with cytoplasmic dynein intermediate chain - like protein at 67 kda in lily pollen. under confocal laser scanning microscopy after immunoflurescence labeling, we found that the dynein intermediate chain - like protein appeared punctated and was co - localization partly with microtubules in cytoplasm of lily pollen tube

    免疫熒光標記及激光共聚焦掃描顯微鏡觀察發現，類細胞質力蛋白中間鏈在百合花粉管中存在於顆粒狀細胞器上；免疫熒光雙標及激光共聚焦掃描顯微鏡觀察發現，百合花粉管中類細胞質力蛋白中間鏈和微管存在部分共分佈。
  4. Based on the reseaching of lycoris leaf micro - morphology characters by sem scanning, light microscope viewing and using paraffin method in the article, we try to provide the proofs of experiment and the efffective characer indexes to discuss the system and evolution of the lycoris. we find these microscope characers through reseach are as follows : the arrangement type, density and the length of stoma ; the shape and length of the epidermal cells ; the ridge of epidermis ; the transverse shape of leaf ; the number of the vascular bundle ; the style of vessel arrangement of vascular bundle in the middle vein ; the layers of palisade tissue ; the ratio of the thicken of palisade tissue to that of spongy tissue ; the angle number of the middle leaf ; the type of ventilating cavity etc. these characters are different from those of species in lycoris, meanwhile these characters are similar to those of some species in lycoris. so these characters can be used as the character indexes for differentiating species and reseaching systematic evolution of lycoris ; we can divide lycoris into two subgenus by these characteristic indexes : the species of one subgenus are l. aurea ( l " her. ) herb, chinensis traub, l. caldweuii traub, l. anhuiensis y. hsu et q. j. fan, l. longituba y. hsu et q. j. fan ; the species of another subgenu s are l. houdyshelii traub, l. albiflora koidz.,

    研究結果表明：葉表皮的氣孔排列方式、長度、長寬比，脊的明顯與否，葉表皮上的顆粒紋飾的多少、大小，葉表皮細胞長度、長寬比、垂周壁形狀，上部葉柵欄組織細胞層數、葉的維管束數、葉中脈導管組成數目，氣腔類型，葉的脊部遠軸面的角數，葉緣的形狀等這些特徵在種間存在差異，同時，在有些種之間又有相似性；因此，這些特徵既可以作為區分種的證據，又是研究石蒜屬植物系統演化的性狀指標，根據這些性狀指標，可以將石蒜屬植物大致分為兩個亞屬：一是忽地笑、中國石蒜、短蕊石蒜、安徽石蒜、長筒石蒜，二是江蘇石蒜、乳白石蒜、石蒜、玫瑰石蒜、稻草石蒜；在兩個亞屬中其中有些種如忽地笑、長筒石蒜、中國石蒜的親緣關系則更近些。
  5. After the recombinant plasmid pcdna3. 1 / ts87 was identified by digestion of hindlll and bamh i, it transformed into cos7 by lipofectamine. expression product was identified by immunohistochemical method, sds - page and western - blot. the immunocytochemistry result has shown that specific brown - staining grains were found in the cytoplasm of cells transformed by recombinant plasmid versus not seen in cells transformed by pcdna3. 1 or normal cells ; the sds - page result has revealed that a band about 3 8kb was found in cell lysis transformed by recombinant plasmid versus not in cells transformed by pcdnas. l or normal cells ; the western - blot result has showed that only the band about 38kd was recognized by sera from rabbit infected by t. s artificially and sera from rabbit immunized with soluble antigen of t. s and with protein expressed by ts87 gene and by a monoclonal antibody of t. s

    通過細胞的免疫組化，細胞裂解物的sds - page電泳， westem - blot分析檢測目的基因的表達情況。免疫組化結果顯示：重組質粒轉染的細胞質中有棕褐色顆粒，而空載體轉染細胞及正常細胞無此現象；細胞裂解物sds - page電泳結果顯示：只有重組質粒轉染的細胞在約38kd處有明顯的蛋白帶，這與理論計算的ts87基因表達蛋白的分子量為38kd基本一致； western - blot分析結果顯示：約38kd的蛋白帶能夠分別被旋毛蟲感染兔血清，成蟲蟲體可溶性抗原免疫兔血清， ts87基因原核表達蛋白免疫兔血清（ ts87血清）以及一株具保護性的旋毛蟲單抗特異識別。
  6. Transfection of cell lines impaired for vzv infection with a plasmid expressing human ide resulted in increased entry and enhanced infection with cell - free and cell - associated virus

    Vzv感染受抑制的細胞系通過質粒表達轉染人類ide蛋白后可增加游離病毒顆粒以及細胞內病毒引起的感染。
  7. Here we report that growth cones of rat cerebellar axons in culture turned away from a gradient of sdf - 1, a chemokine that attracts migrating leukocytes and cerebellar granule cells via a g protein - coupled receptor ( gpcr )

    以前的證據表明， sdf - 1 ，一種經典的chemokine ，能夠吸引白細胞和遷移中的神經元，這種作用是通過g蛋白耦聯受體介導的。利用生長錐轉向分析，我們發現sdf - 1的濃度梯度能夠吸引或排斥培養的小腦顆粒細胞的生長錐。
  8. Renin, a proteolytic enzyme formed in the granules of the juxtaglomerular apparatus cells, catalyzes conversion of the protein angiotensinogen to angiotensin i, a decapeptide

    腎素是腎小球旁體細胞顆粒內形成的一種蛋白水解酶，催化蛋白血管緊張素原轉換為血管緊張素，即十肽。
  9. Granulocytic sarcoma ( gs ), also known as extramedullary myeloblastoma or chloroma is an unusual manifestation and represent soft tissue masses composed of immature cells of the granulocytic series

    顆粒性白血球肉瘤也稱為骨髓胚細胞瘤或綠色瘤，是一種少見的疾病。
  10. The second medium included egf ing / ml and igf - 1 long / ml in addition to the control. likewise, the last medium contained 50 % granulosa cells conditioned medium. oocytes were cultured for 16 or 18 hours, and only the oocytes underwent first polar body extrusion were collected for future study

    Inmegflug ml十igf 110ng ml ）和顆粒細胞生長液組乃0顆粒細胞生長液） ，對昆明白小鼠生發泡期（ ge訕nalvesicle ， gv ）卵母細胞進行體外成熟培養； 5
  11. Methods 50 wistar rats were sensitized by ovalbumin as animal model of ar and randomly divided into 5 groups : model group, ketotifen fumarate group, xinqin granules group, low - dose minkang tablet group, and high - dose minkang tablet group, another 10 healthy rats in normal group

    方法除正常組外，其餘大鼠用卵清蛋白造成變應性鼻炎模型，隨機分為模型組、西藥對照組（酮替芬組） 、中藥對照組（辛芩沖劑組） 、敏康片小劑量組、敏康片大劑量組；用藥1周后觀察大鼠一般情況及鼻黏膜肥大細胞數、脫顆粒細胞數、血漿組胺的變化。
  12. 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。
  13. Anti - p21 mouse monoclonal antibody from beijing zhongshan biotechnology anti - mouse or anti - rabbit igg secondary antibody from santa cruz biotechnology ly294002 from sigma biotechnology tritonx - 100 from boehringer mannhein gmbh fluorescein isothiocyanate ( fitc ) conjugated anti - mouse igg antibody was purchased from beijing zhongshan biotechnology hepes from e. metck darmstadt methods superovulation and collection of eggs for superovulation, female kunming mice 4 - 5 week old were injected with pregnant mare serum gonadotropin ( pmsg ), and after 46 - 48 hours with human chorionic ginadotropin. ( hcg ). one - cell fertilized eggs were collected on the next day from oviduct of females

    取4一5周齡成熟雌性昆明系小白鼠，腹腔注射pmsg （孕馬血清促性腺激素） 10iu ， 46一48小時后腹腔注射hcg （人絨毛膜促性腺激素） 1oiu ，將注射hcg后的雌鼠與8周以上的成熟雄鼠合籠交配，次日檢察陰栓，將查到陰栓的雌鼠處死，取輸卵管于mz培養液中，解剖鏡下撕開壺腹，釋放細胞團，然後用300林歲nil透明質酸酶消化去除顆粒細胞，口控吸管將卵細胞在m :中反復清洗，然後置於孵箱中，根據時間點收集g2期細胞。
  14. In this experiment hcv structural gene was amplified by polymerase chain reaction ( pcr ), and was inserted into baculovirus expression vector pfastbacl to construct a recombinant transposing vector pfbl - cee. the plasmid pfb 1 - cee was transformed into dh1 obac competent e. coli cells. high molecular weight dna was prepared from the overnight cultures from the selected e. coli colonies, which was recombinant baculovirus shuttle vector containing hcv structural gene, named bac - cee

    本實驗用pcr擴增hcv結構區基因，克隆到桿狀病毒表達載體pfastbacl中，構建成重組轉座載體pfb1 - cee ，轉化dh10bac大腸桿菌感受態細胞，篩選陽性菌落，抽提大分子質粒dna ，獲得含hcv結構區基因的重組桿狀病毒穿梭載體bac - cee ，脂質體介導轉染sf9昆蟲細胞，出現細胞病變后，收集含有重組桿狀病毒顆粒的培養上消，重新感染sf9細胞，收集sf9細胞，進行12 . 5 sds -聚丙烯酰胺凝膠電泳，可見表達的蛋白條帶。
  15. Human granulosa cells isolated from follicular fluid of 16 patients received ivf or icsi were cultured in tcm199 medium. granulosa cells were examined to detect fshr by immunobiochemistry assay and rt - pcr. 3

    對16例接受體外受精患者卵泡液中分離的卵巢顆粒細胞進行體外培養，利用免疫組化法和rt pcr法檢測顆粒細胞的fshr的蛋白表達和mrna的表達，鑒定體外培養顆粒細胞的純度； 3
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