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binding affinity中文是什么意思

  • 結合親和力
  • 親合力

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  • 例句與用法
  • The binding affinity of remaining hemoglobin sites for oxygen is changed by the presence of co binding .
    氧在血紅蛋白其余位置上的鍵合力被一氧化碳所改變。
  • The high binding affinity and selectivityin conjunction with the polymers ' physical robustness positions molecular imprinted polymers ( mips ) as candidates for use as preliminary screens in drug discovery
    聚合物的高親和力、高選擇性及物理性質穩(wěn)定特點使得分子印跡聚合物可用于藥物開發(fā)中的初篩。
  • Correspondingly , the egf binding affinity of surface egfr and the tyrosine auto - phosphorylation of immuno - precipitated egfr were also enhanced in gntv - s / h7721 cells and reduced in gntv - as / h7721 cells
    Egfr的信號通路主要有兩條,一是ras - raf - mek一mapk經(jīng)典途徑,另一條是新發(fā)現(xiàn)的pi一3k一pkb途徑。
  • Detection of antigen - binding affinity of soluble mg7 scfv elisa was adopted to examine the antigen - binding affinity of soluble mg7 scfv ; competitive elisa was performed to test the inhibitory ratio of soluble mg7 scfv to the binding affinity of mg7 mab with its relevant antigen
    El舊a拐成惴現(xiàn)2個克隆的可容牲mg7seem明顯的抗原結合舌隊其a分別為0 832和0 912 ,均高出附性對照( 0
  • Detection of antigen - binding affinity of mg7 recombinant phage antibody elisa was repeated to confirm the antigen - binding affinity of positive clones screened out in the former procedure ; these positive phages were examined by restriction analysis ( ecor i and hind iii ) ; competitive elisa was performed to test the inhibitory ratio of these positive clones to the binding affinity of mg7mab and its relevant antigen , the positive dones possessing apparent inhibitory effect were singled out for later use
    X陽性克到駛知烘扳原kbbjg )濁對陽性克隆進行限制隴臥賜析( uwi和hedlll )鑒定三用競爭elisatoljmg7重組噬菌體抗體性克隆對mg7單扶與其相應抗原結合忙的喇率,從中j ) ed出對mg7單抗與期??乖Y合有抑余j效應的克隆用于進一涉研究。
  • The experimental method includes selecting pure complexes of histidine - containing or cysteine - containing materials , from c - and n - terminal group of these amino acids to link to a group which have color or fluorescence or ultraviolet absorption , elucidating their binding affinity , fluorescence or uv - visible spectrum properties with zinc at physiological concentration and to elucidate their structure in the solid state via infrared spectroscopy . with the help of the concerned the data , the analysis was done to prove whether it can be applied to the zinc detection , in other words , whether it can be used as a new fluorescence probe for zinc detection
    本實驗首次選用在生物體內(nèi)與zn ~ ( 2 + )鍵合能力很突出的物質? ?組氨酸和半胱氨酸,采用類似于多肽合成的方法,在其羧基或氨基分別嫁接上一個帶有標記的基團,生成穩(wěn)定的共價鍵化合物;在此化合物中模擬生理濃度條件加入鋅離子,通過紅外圖譜、紫外圖譜或熒光圖譜的變化分析鋅離子對標記基團是否產(chǎn)生影響,再結合有關數(shù)據(jù)分析其是否適合檢測鋅離子,即是否可能作為新的鋅離子熒光探針。
  • Reports about great enthusiasm in the synthesis of the complexes of rare earth medicine , the interaction of the rare earth complexes with dna are very few in the world . it is expected to explore the mechanisms of interaction that are used to offer an opportunity to understand which parameters affect the binding mode and binding affinity to dna . part ii
    從這些總結中了解到,人們之所以選擇蘆丁作為小分子配體,是由于蘆丁所具有的特性:它屬于黃酮類化合物,具有獨特的藥用價值及其臨床應用價值,更令人興奮的是它還具有良好的電活性,這樣就可以利用電化學方法來研究其作用機理。
  • Culture of mg7 hybridoma cells and detection of antigen - binding affinity of mg7 mab by elisa 2 . construction and identification of mg7 recombinant phage antibody library mrna was isolated from cultured mg7 hybridoma cells and converted into cdna ; the variable fragments of heavy and light chain were separately amplified and assembled into scfvs with a specially constructed dna linker by pcr . the scfvs dma was ligated into the phagmid vector pcantabse and the ligated sample was transfered into competent e . co / / tg1 to generate a bacterial form of mg7recombinant phage antibody library ; volume and recombinant ratio of the library were evaluated by means of bacterial colony counts and restriction analysis ( ecor i and hind iii )
    Mg _ 7重組噬菌體抗體庫的構建及鑒定從培養(yǎng)的mg _ 7雜交瘤細胞中提取并分離mrna ,反轉錄成cdna ;利用pcr分別擴增mg _ 7單抗的重鏈及輕鏈可變區(qū)基因,并通過? dna連接子將二者連接起來形成mg _ 7單鏈抗體基因;將mg _ 7單鏈抗體基因插入pcantab5e ;將連接產(chǎn)物轉化感受態(tài)tg1大腸桿菌,制備細菌形式的mg _ 7重組噬菌體抗體庫;通過菌落計數(shù)和限制性酶切分析( ecor和hind )評估m(xù)g _ 7重組噬菌體抗體庫的容量和重組率。
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