labeled by 中文意思是什麼
labeled by
解釋
用. . . . . . 標記-
6. oocytes were fixed for immunofluorescence. examination of cgs and microtubules were performed by fitc labeled lens culinaris agglutinin ( lca ) and and - fi - tubulin under confocal scanning laser microscopy ( cslm ) respectively
利用直接免疫熒光染色和共聚焦顯微鏡（ confocalscan muglasermicroscopy ， cslm ） ，研究各組體夕成熟卵的皮質顆粒和微管 -
If i want to elucidatied the complax problem, i had to analysis it from many aspacts. in the historical context in china then. the transmit had the historical invialibility. and the evolution acted as the historical invialibility by accident. our tranditional culture and the science practice in ancientry society offered the theory chance for the transmit. finally, the evolution labeled by science
在當時中國的歷史情境下，這種傳播是有其歷史必然性的。而進化論就偶然地充當了這種歷史必然性。而我國的傳統文化和古代社會的科學實踐則為這種傳播提供了理論契機和物質基礎。 -
Our previous studies showed existence of apoplast cam in the plant cell and cam had many extracellular functions. so it supposed cam may be one of important extracellular polypeptides and trigger the intracellular signal transduction by binding the receptor. in this study, radiolabelled ligand is used to investigate the binding characteristic of cam and a. thaliana protoplasts. and chemical crosslinking is employed to explore binding proteins in the membrane. at first, ( 35 ) ~ s - cam was produced using ( 35 ) ~ s - labeled amino acid mixture in e. coli. sds - page and autoradiograph indicated high - purified, high - specific radioactivity ( 35 ) ~ s - cam was obtained. electrophoresis of ( 35 ) ~ s - cam is the same as that of unlabeled cam with ca ~ ( 2 + ) or egta ; a quatitive of protoplasts was prepared by enzymolysis
首先，用~ （ 35 ） s標記的氨基酸混合物喂養工程菌成功地制備了~ （ 35 ） s標記的擬南芥鈣調素（ ~ （ 35 ） s - cam ） ， ~ （ 35 ） s - cam純度高、放射活度高、 ca ~ （ 2 + ）與egta存在時的電泳行為與未標記cam相同，可作為一種高靈敏性的探針用於進行受體學分析實驗；用擬南芥種子誘導愈傷，通過酶解制備了大量原生質體。 -
Other commentators, inspired by james frazer ' s theories, have additionally labeled mithras a mystery religion with a life - death - rebirth deity, comparable to isis, the resurrected jesus or the persephone / demeter cult of the eleusinian mysteries
其他評論，受啟發于詹姆士的理論，加之又把密特拉教套上神秘宗教的標簽，是生命?死亡?再生的神性，可與伊希斯，耶穌的復活或者古代希臘神秘的帕爾修斯/得墨忒耳的祭禮相比較。 -
In this study, in order to examine the dynamics of tip [ ca2 + ] i together with the dynamics of tip - localized f - actin in vivo, a kind of double labeled material was constructed. the ca2 + and actin microfilaments of arabidopsis pollen tubes were labeled by cameleon and gfp - mtalin respectively
本研究以擬南芥花粉管為材料，通過轉基因技術，將分別標記ca ~ （ 2 + ）和微絲的兩種熒光蛋白cameleon與gfp - mtalin在花粉管中同時表達，實現活體花粉管中ca ~ （ 2 + ）與微絲的同時標記。 -
The his - tagged peacl - gfp purified from the supernatants could polymerize into green fluorescent filamentous structures with diameter, length and shape being identical to that of muscle f - actins, which could be labeled by tritc - phalloidin ( a specific agent for staining actin microfilaments ), and were identified as having a 9 nm diameter by negative staining, corresponding with that of the muscle f - actins ( 7 - 10 nm ). under polymerization conditions, his - tagged peacl - gfp polymerized with kinetics similar to those of skeleton muscle actin, that is, an obvious lag nucleation period at the beginning of polymerization and an s - like typical polymerization curve could be obtained. the critical concentration is 0. 75 umol / l near to that of chicken muscle actin ( 0. 56 umol / l ) under the same condition
熒光標記結合熒光顯微觀察表明：從可溶性上清中純化的his - taggedpeac1 - gfp聚合形成的微絲不僅可以直接在熒光顯微鏡下觀察，也可被微絲的特異標記物鬼筆環肽所標記，而且其直徑、長度以及形態上與已知的聚合肌動蛋白熒光絲一致；電鏡負染的結果進一步證實其直徑為9nm ，與傳統微絲直徑相當（ 7 ? 10nm ） ；聚合曲線有明顯的停滯期，為典型的s型聚合曲線，聚合臨界濃度為0 . 75 mol l ，這一結果與已有報道相似。 -
Hybridization bands were detected by southern blot analysis using lea3 gene probe labeled by digoxigenin the result showed that foreign lea3 gene integrated into strawberry genome
2 。對點雜交為陽性的植株進行southernblot分析，轉化植株檢測到了雜交帶，除預期的1 -
The 2nd pair of primers was designed according to the sequence of strain th - 98 collected in genbank. concentration of tp was analyzed after amplification invitro by rt - pcr, purified by low melt agarose and labeled by digoxigenin
根據genbankth - 98株序列設計第2對引物，應用rt - pcr方法體外擴增該片段（命名為tp ） ，瓊脂糖凝膠純化后測定其濃度和純度，進行非放射性地高辛標記。 -
One was cloning, sequence analysis and expression of the fragment containing the b and c antigenic sites locating at the 5 " terminus in spike gene of tgev in prokaryotic expression system ( fused with gst ), the other was preparation of non - radioactive probe labeled by digoxigenin for detecting the rna extracted from tgev by assay of dot - blot
為了鑒別診斷tgev與prcv及對tgev進行流行病學調查，本研究採用原核表達系統（ gst融合表達系統）表達tgev纖突蛋白（ s蛋白）中含有b和c抗原位點的多肽，並且制備了非放射性地高辛標記的核酸探針，通過斑點雜交（ dot - blot ）檢測tgev核酸rna 。 -
Lea3 gene probe and marker probe were labeled by dig - chem - link
Okblea3片段，並用地高辛標記法進行了lea3基因探針的制備。 -
Was multiplied and the tk gene was cloned. the cloned tk gene was retrieved by proper restrictive hemodynamics. the retrieved tk gene was labeled by digoxin according to the kit of labeling and detection of digoxin. then, the specificity and sensitivity of tk gene probe were detected with dot blot hybridization. the sequence of tk gene of nm98a strain was analysed. the result of the analysis of tk gene ' s sequence confirmed that autoploidy between tk gene of nm - 98a strain and issued strain was 99. 7 %
本研究中首次對iltv - nm98a株的tk基因進行了克隆和序列分析，結果表明： iltv - nm98a株tk基因的核苷酸序列與已發表的iltvtk基因的核苷酸序列具有高度的同源性，兩者之間僅相差4個核苷酸，同源性高達99 . 7 ，從而證實了iltvtk基因是高度保守的，為iltvtk基因核酸探針的制備提供了有力的依據。 -
Construction of recombinant adeno - associated virus vector expressing glial cell line - derived neurotrophic factor labeled by green fluorescent protein
綠色熒光蛋白標記的大鼠膠質細胞源性神經營養因子重組腺病毒載體的構建及其表達 -
Another detection method, dot blotting, was built also based on 35s promoter and nos terminator. the two genes were labeled by digoxin to done as probe used in dot blotting
並將35s啟動子和nos終止子用地高辛標記后制備成基因探針，建立了轉基因檢測的分子雜交技術?點雜交。 -
In 1903, the boundary of the " city of victoria " was gazetted by the government and was labeled by boundary stones
1903年，政府在憲報頒布法令界定維多利亞城范圍，並豎立界石標明範圍。 -
From linguistics, cognitive psychology and computational linguistics, we searched the base of theory of key phrases ' advantage, defined key phrases, and acquired them by extracting key words labeled by specialist in web pages
本文從語言學、認知心理學和言語習得、計算語言學等方面尋求關鍵短語優勢的理論依據，對關鍵短語進行了界定，通過抽取網頁上專家標引的關鍵詞獲得關鍵短語。 -
Thin sections of host leaf cells infected by bbwv - 2 isolate b935, which were gold - labeled by antibodies of bbwv - 2 coat protein ( cp ) and vp37, respectively, were prepared to elucidate the locations of vp37 in cell and possible function of vp37 and cp in cell to cell movement. observation in electron microscope showed that virus particles were presented not only in cytoplasma but also in chloroplast, while vp37 was existed only in cytoplasma and associated with tubular structure through the cell wall
為研究vp37在寄主細胞中的作用機制及其在細胞中的分佈，通過膠體金間接標記6his - vp37兔抗血清，同時還標記了病毒的外殼蛋白單克隆抗體，對bbwv - 2分離物b935感染的病葉超薄切片的電子顯微鏡觀察發現：病毒粒子除了聚集在胞質中，還存在於寄主的葉綠體內； vp37蛋白能在細胞壁上形成管狀結構，在胞質中亦有分佈。 -
The standard and comparative samples needed by the port inspection offices shall be examined and labeled by the national institute for the control of pharmaceutical and biological products
口岸檢驗所需標準品、對照品由中國藥品生物製品檢定所負責審核、標定。 -
Correct clones were selected and plasmid dna was isolated and digested with saci and puvii. a dna fragment of about 2. 1kb was purified and labeled by dig - 11dutp as probe. at least 40 positive clones were obtained from human genomic library by in situ colony hybridyzation with this probe. among them one clone contains human serum album dna by sequence
以pcr擴增的人血清白蛋白（ hsa ）基因片段為探針，從人的基因組文庫中雜交篩選的陽性克隆中，經測序分析，有一個克隆含有全長hsadna ，用從其它的陽性克隆中選取兩種dna片段，即dna修復基因hfen1和一段非編碼大片段cit987sk - 384d8 ，與人hsadna一起，進行顯微共注射，成功制備了轉多基因小鼠。 -
Despite its popularity, starbucks has been criticized and labeled by many as a blood - sucking corporate machine, driving smaller coffee shops out of business through unfair practices
盡管受歡迎，但星巴克還是被有些人指責或標榜為「吸血鬼機器」 ，因為它的壟斷使得許多小型咖啡企業破產。 -
A novel real - time fluorescent rt - pcr was established to detect pnrsv this technique uses a taqman probe to monitor in real time amplification of target genes, a taqman probe labeled by a quenching and fluorecenting was added to the pcr reaction buffer
另外還設計了taqman熒光探針，確定了檢測條件和參數，建立了實時熒光rtwcr方法，該方法是指在pcr反應體系中加入帶有熒光基團互補探針，如果有pcr反應（擴增） ，熒光信號就較大。
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