染色鏡檢 的英文怎麼說

中文拼音 [rǎnshǎijìngjiǎn]
染色鏡檢 英文
microscopic examination of stained preparation
  • 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
  • 鏡 : Ⅰ名詞1 （鏡子） looking glass; mirror 2 （幫助視力或做光學實驗的器具） lens; glass 3 （姓氏） a s...
  • 檢 : Ⅰ動詞1 （查） check up; inspect; examine 2 （約束; 檢點） restrain oneself; be careful in one s c...
  • 染色 : dye; dyeing; colouration; tintage; tinging; dyschroia; colouring; colour; [半] decoration染色不足...
  1. Comparison of results of pcr and gram staining microscopic examination for chronic gonorrhea

    檢測法與革蘭氏染色鏡檢法同時檢測慢性淋病結果的比較
  2. Histology : the study of the structure of tissues by means of special staining techniques combined with light and electron microcopy

    組織學：以特殊的染色技術以及光學顯微鏡和電子顯微鏡檢查、研究組織結構的學科。
  3. 4 forty - eight volunteers had two " jumbo " biopsies taken from the gastric antrum for examination with rapid urease test, improved giernsa stains and h & e in order to diagnose helicobacter pylori ( hp ) infection and evaluate inflammation of gastric mucosa

    448例志願者均行胃鏡檢查，取胃竇組織活檢，分別行快速尿素酶試驗、改良giemsa染色和病理he染色，以確定有無幽門螺桿菌（ helicobacterpylori ， hp ）感染和胃黏膜有無慢性炎癥。
  4. Sections were stained by he and were observed under light microscope. ( 4 ) observation on cell - matrix complex with confocal microscope. cell - matrix complex was stained by fluorochrome cfda - am ( loug / ml, looul ) after 7 days incubation, the sample was scanned by confocal microscope to observe cell - growth in the matrix

    細胞一多孔膜復合物的激光共聚焦顯微鏡觀察：取培養7天的細胞一多孔膜復合物，以10ug inl的熒光染料cfad am100ul染色，檄光共聚焦顯微鏡檢測激光激發的綠色熒光，掃描成像觀察活細胞生長倩況。
  5. According to the gene sequence and secondary structure of hcv ns5b, we design the sirnas targeting ns5b gene following with the requirement for sirnas design from tuschl et. al and synthesize it from dharmacon company ; hepg2 cell stably expressing ns5b - egfp protein was trasfected by synthesized sirnas with electroportion, the non - transfected cell and non - specific sirnas transfected cell are c onsidered as control group ; inhibitory effect of sirnas was investigated by fluorescence microscope with dapi dyeing and by semi - quantitative rt - pcr

    然後根據dsrna設計原則，結合nssb基因的序列特徵，藉助生物信息學軟體設計了針對nssb基因的sirnas ，並交由公司化學合成；電穿孔法轉染上述穩定轉染的細胞克隆，同時分別以非特異的sirnas轉染組和空白轉染組為對照， dapi染色后通過熒光顯微鏡和內標化rtpcr檢測，初步證實了化學合成的sirnas可以特異阻斷nssb基因的表達。
  6. Light microtechnique and sa - galactosidase method was used to study the effects of super - high - concentration of glucose on the senescence of human diploid fibroblast 2bs cells, ros and the membrane potential of mitochondria during this process were measured. our results showed that 200 mmol l of glucose inhibited the growth of 2bs cells, led to the changes of reactive oxygen species and decrease of mitochondrial membrane potential, and caused senescence of 2bs cells rapidly. it supports the hypothesis of oxidative damage of senescence. moreover it is a better system for the study of the effects of ros during the process of replicative senescence

    利用光學顯微鏡觀察和酸性-半乳糖苷酶染色技術研究了高濃度葡萄糖對人二倍體成纖維細胞2bs細胞衰老進程的影響，並用流式細胞儀檢測了此過程中活性氧和線粒體膜電位差的變化。結果表明： 200 mmol l的葡萄糖對2bs細胞有生長抑制作用，能引起活性氧含量的變化，導致線粒體膜電位差顯著下降，並誘導了細胞的衰老。這為氧化損傷假說提供了新的證據，並為研究活性氧和復制衰老之間的關系提供了較好的體系。
  7. Thirdly, the new method and nearest - neighbor method, single linear interpolation, bilinear interpolation were coded by vc + +, and a mfc application, bmpinterpolation, was achieved. many kinds of examples were tested using bmpinterpolation, including single color images and true color images ( 24bits ), photos and images after 3d rendering by 3dmax. the comparison between new method and the others indicates that the new method can not only get higher quality of images but also match the requirement of procedure speed

    用該程序可以實現了對單幅位圖文件的讀取和插值放大，通過單色和彩色圖像、照片圖像、三維渲染圖像等放大處理算例的檢驗，說明了本文的方法和程序是成功有效的，新演算法明顯優于幾種簡單插值放大方法的輪廓清晰度，且具有很好的快速性，兼顧了自動立體鏡三維顯示的快速性和清晰度要求。
  8. Methods : in cultured lung explants without serum, the lipid component synthesis of pulmonary surfactant was evaluated in [ 3h ] - choline incorporation ; mrna content of phosphocholine cytidylyltransferase ( cct ) in lung explants was investigated in rt - pcr ; the changes of the ultrastructure of the at ii cells were observed with electron microscope ; the expression of nmdar1 subtype was observed in immunohistochemistry staining ; nitric oxide synthase ( nos ) activity, nitric oxide ( no ) content, superoxide dismutase ( sod ) level, malondialdehyde ( mda ) content and lactae dehydroase ( ldh ) level were determined by biochemistry methods. results : 1. influence of glutamate on synthesis of the lipid component of pulmonary surfactant ? with l - arginine, glu inhibited [ 3h ] - choline incorporation with good dose - dependence and time - dependence ; ( 2 ) mrna content of cct of the glu treatment groups was decreased ; ( 3 ) glu increases the release of ldh in cultured lung explants ; ( dwith electron microscope histochemistry, glu induced the changes of the ultrastruture of at ii iv cells

    方法：採用成年大鼠肺組織無血清培養，運用[ ~ 3h ] -膽堿摻入法測定ps主要脂質磷脂酰膽堿（ pc ）合成量； rt - pcr擴增檢測肺組織中pc合成限速酶磷酸膽堿二胞苷酰基轉移酶（ cct ） mrna含量；透射電子顯微鏡法觀察肺泡型上皮細胞和ps系統超微結構的變化；免疫組織化學染色檢測glu的受體nmdar1亞單位的表達；生化測定肺組織乳酸脫氫酶（ ldh ）釋放量和肺組織勻漿中一氧化氮合酶（ nos ）活性、一氧化氮（ no ）生成量、超氧化物歧化酶（ sod ）水平以及丙二醛（ mda ）含量。
  9. To confirm the approval of recombinant pcdnas - tgfjtf, gene and the results of its transfection, we used immuhistochemical staining ( sabc ). the department of or a logy 4 multiplication and differentiation of bmscs were observed by flow - cytometry ( tcm ), transilluminating electron microscope ( tem ) and other methods. the bmscs in controlled group was transfected with pcdna3 only

    採用電泳檢測pcdna3 - tgf _ 1構建是否成功；通過tgf _ 1免疫組化染色檢測轉染是否成功；運用形態學觀察、透射電鏡（ tem ） 、流式細胞儀（ fcm ） 、堿性磷酸酶（ alp ）染色、型膠原免疫組化染色等方法，觀察轉染后bmscs增殖與分化情況。
  10. We also stained the embryos with anti - arp3 antibody and found that these two kinds of antigen are generally co - localized but arp3 were not detected in cleavage stage embryos. it was deduced that cortactin functions in the cytokinesis independent of arp3. and microinjection of anti - cortactin antibodies into the i cell stage embryos leaded to fatal developmental defects because of the unequal cytokinesis

    在利用抗ap3的抗體進行的胚胎整裝染色中，激光掃描共聚焦顯微鏡觀察發現， arp3在卵裂期沒有表達， mbt后，在細胞皮層區檢測到arp3蛋白的陽性染色，在隨后的發育過程中arp3與皮層蛋白共分佈。
  11. This study we acquired the coding region of hcv ns5b gene by pcr of hcv full length genome and construct the recombinant plasmid pegep n3 - ns5b ; with the different concentration of g418 in the culture medium, we think the selection concentration of g418 for hepg2 cell is 800 g / ml ; the recombinant plasmid was transfected into hepg2 cell by lipofectamine2000 cells containing stable transformants were selected by the ability of resistance to g418 and isolated with the limited dilution. the stably transfected cell line expressing ns5b - egfp fusion protein was obtained by the detection under fluorescence microscope and rt - pcr

    本研究首先從hcv基因組中擴增出nssb基因，構建了nssb基因與報告分子egfp （增強型綠色熒光蛋白）基因的融合基因真核表達質粒pegfpn30 ；通過含有不同g418濃度梯度的培養液培養hepgz細胞，確定了篩選用g4181作濃度為800pg ml ；利用脂質體法將該重組質粒轉染hepgz細胞，經過有限稀釋法和g4壓力選擇，應用熒光顯微鏡和rtpcr檢測，獲得可穩定表達nssbegfp融合蛋白的hepgz細胞克隆。
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