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total cells
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  细胞总数
     The ratio of Kupffer′s cells in the right and the left lobe to the number of total cells was distinctly different(the left lobe:4.054%±1.642%, the right lobe:1.261%±0.536%) (P<0.05).
     左、右叶库普弗细胞数占细胞总数的百分率明显不同(左叶:4·054%±1·642%,右叶:1·261%±0·536%)(P<0·05)。
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     And CD86~+mDCs were 87% in total cells after culture 48 hours with rhGM-CSF,IL-4 and TNF-α in vitro.
     再加入rhGM-GSFI、L-4和TNF-α培养48 h后,CD86+mDC占细胞总数的87%。
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     S-100 protein positive imDCs were 96.9% in total cells after cultured for 6 days with rhGM-CSF and IL-4 in vitro.
     体外加入rhGM-CSF和IL-4培养6d后,S-100+imDC占细胞总数的96.9%;
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     On day 0,6,10 and 14, total cells were counted, CD34+, CD34+CXCR4+ and CD34+CD49d+ cells were quantitated by FACS, and hematopoietic progenitor cells were assessed by semisolid culture assay.
     在0、6、10及14天检测细胞总数、CD34+细胞数及集落形成单位(CFU)数,同时检测CD34+细胞上CD49d+及CXCR4的表达数。
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     When cell differentiation occurred, NSE positive cells were 24.76%± 2.72% at the most and GFAP positive cells were 36.58%±3.26% of total cells.
     细胞分化后 ,NSE阳性细胞最多占细胞总数的 2 4 .76 %±2 .72 % ,同时 GFAP阳性细胞占细胞总数的 36 .5 8%± 3.2 6 %。
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  “total cells”译为未确定词的双语例句
     Results:(1)The expression of positive rate of P65,P50and IKB in cytoplasmwas76.9%,81.8%and84.6%respectively,and the significant positive expression of P65and P50was also found in nuclear,with a rate of15.3%,45.5%respectively,the expression of positive rate of MDM2was38.5%in total cells.
     结果 :(1)P65、P50及IKB在胞浆内表达阳性率分别为76 9 %、81 8 %、84 6 %,P65、P50在胞核内表达阳性率分别为15 3 %、45 5 %,MDM2蛋白表达阳性率为38 5 %。
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     The counts of neutrophils in the TCEs were 1.22×10 6±4.75×10 5, comprising 4.2±5.4% of the total cells.
     而嗜中性白细胞总数和百分比分别为 1.2 2× 10 6 ± 4 .75× 10 5/ ml和6 4 .2 %± 5 .4 % ;
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     From 0.1, 0.2, 0.4, 0.6 to 0.8 g·L -1 treatment groups , the rate of apoptotic cells to total cells were 3.1%, 2.5%, 13.3%, 40.4%, 48.6%, respectively, and what in the control group was 1.4%;
     0 .1,0 .2 ,0 .4 ,0 .6 ,0 .8g·L-1各处理组凋亡细胞比率分别为 3.1% ,2 .5 % ,13.3% ,4 0 .4 % ,4 8.6 % ,对照组为1.4 % ;
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     the rate of S phase cells to total cells was 28.6%, 17.5%, 19.1%, 14.2%;
     S期细胞比率分别为 2 8.6 % ,17.5 % ,19.1% ,14 .2 % ;
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     2n = 37(61% total cells observed),and the formulas of two patterns of karyotype are:K = 2n = 38 = 12Am + 14Bm+ 12Bsm_1K = 2n = 37 = 15Am +10Bsm + 12Bsm_1of those 111 cells in metaphase,7 cells were photographed and enlarged by means of a microscopic and enlarging measurement.
     两种核型的核型公式分别为: K=2n=38=12Am+14Bsm+12Bsm_1 K=2n=37=15Am+10Bsm十12Bsm_1。
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     U cells.
     Li/TK细胞3d,即可将其杀死.
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     The total cells and eosinophils were counted in the BALF.
     计数BALF中的细胞总数及嗜酸性粒细胞(EOS)的个数。
短句来源
     The total cells and eosinophils were counted in BALF.
     计数BALF中的细胞总数及嗜酸性粒细胞(EOS)数。
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     total ISp].
     total 15μl。
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     The whole cells of R.
     直接将霉菌R.
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  total cells
The number of viable and total cells was measured by the number of colonies and optical density, respectively.
      
Neurons labelled for preprosomatostatin mRNA with either RNA or DNA hybridization probes constituted approximately 10% of the total cells and comprised a small cell group that differed in average size from the β-preprotachykinin labelled population.
      
The dopaminergic amacrine cells have a low frequency (approximately 1300-1500 total cells in 130 mm2 retina), with their highest density occurring in the visual streak (60 cells per mm2).
      
Under proper cultivation conditions a mitotic index of 77% total cells could be routinely achieved.
      
This increase in bronchopulmonary inflammation was mainly due to a neutrophil and macrophage infiltration, representing 60% and 35% of the total cells, respectively.
      
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Systematological and cytological studies, based on the continuous section cutting of the anther cultured in vitro at fixed intervals, showed that callus could be formed by parenehyma cells at the cut end and apex, and in the septum and wall. The pollen grains in the anther disintegrated and died shortly after being cultured.It was observed that only 4 of the 12079 pollen grains in vitro divided once or twice before they stopped doing so. All embryoids originated in the peripheral layer cells of the...

Systematological and cytological studies, based on the continuous section cutting of the anther cultured in vitro at fixed intervals, showed that callus could be formed by parenehyma cells at the cut end and apex, and in the septum and wall. The pollen grains in the anther disintegrated and died shortly after being cultured.It was observed that only 4 of the 12079 pollen grains in vitro divided once or twice before they stopped doing so. All embryoids originated in the peripheral layer cells of the somatic calli. The period of the 39th—49th day after the culture saw quick aging of the calli and abundant development of embryoids. The numbers of chromosomes in calli, embryoids and plantlets were examined and the result revealed that 91.8—95.6% of the total cell division phases contained 28—36 chromosomes, so they were diploids. Genetic performances also proved that anther plantlets could originate from somatic cells.

定期连续切片观察表明,花药断口处、药端、药隔、药壁的薄壁细胞都可形成愈伤组织。花药中的花粉接种后很快解体死亡。在观察的12079个花粉中,只见4个花粉分裂1~2次也就停止了。全部胚状体来源于体细胞愈伤组织的外围。接种后39~49天的10天期间是愈伤组织迅速衰老,胚状体大量发生的时期。愈伤组织、胚状体和植株的染色体计数发现,染色体28~36条的分裂相占91.8~95.6%,属二倍体。花药植株的遗传表现,也进一步证实植株起源于体细胞。

Testes from seven species of normal adult mammals (rat, mouse, guinea pig, rabbit, bull, ram and swine, ten animals for each species) and eight normal adult men were investigated quantitatively by means of QTM-720 Image Analyser.The spermatogenesis state was assessed by following parameters:A′/N: area of total cells per seminiferous tubule;A″/N:area of cross sections per seminiferous tubule;H:thickness of epithelium of seminiferous tubule.There is a significant difference between various species for these...

Testes from seven species of normal adult mammals (rat, mouse, guinea pig, rabbit, bull, ram and swine, ten animals for each species) and eight normal adult men were investigated quantitatively by means of QTM-720 Image Analyser.The spermatogenesis state was assessed by following parameters:A′/N: area of total cells per seminiferous tubule;A″/N:area of cross sections per seminiferous tubule;H:thickness of epithelium of seminiferous tubule.There is a significant difference between various species for these parameters.A′″/N:mouse>rat> (swine and bull)>(guinea pig, rabbit, man and ram)A′/N:mouse>rat>(swine and bull)>(rabbit, guinea pig, man and ram)H:(swine, mouse and rat)>(rabbit, guinea pig and bull)>(man and ram)The interstitial tissue was assessed by both parameters:(A″—A′)/N:ratio of interstitial tissue area and the number of seminiferous tubules;(A″—A′)/A′:ratio of interstitial tissue area and the total cellular area of seminiferous tubules.There is also a siginificant difference between various species for these parameters: the value of guinea pig is the smallest, while the value of swine is the largest.It was proved that the value of (A″—A′)/N of every species is closely related to the value of (A″—A′)/A′, and eight linear regressional equations were established. All these results have provided important data for further study of male reproductive physiology and male contraception research.

七种正常成年雄性哺乳动物(大鼠、小鼠、豚鼠、家兔、牛、羊及猪,每种10只)及八个正常成年男性的睾丸组织常规石蜡包埋,HE染色切片,摄成照片后输入QTM—720型自动图像分析仪进行定量组织学测定。以每个曲细精管内细胞平均总面积(A′/N)、每个曲细精管的平均截面积(A′″/N)及曲细精管上皮的平均厚度(H)来衡量曲细精管内的精子发生状态。以间质总面积与曲细精管个数的比值(A″-A′/N)及间质总面积与曲细精管内细胞总面积的比值(A″-A′/A′)来衡量睾丸间质的状态。对以上各组测定与计算数据进行了F与t检验。对各组的A″-A′/N及A″-A′/A′进行了回归分析,并求出了八组直线回归方程。结果表明各个物种的精子发生与睾丸间质面积均有其种属特性,这为男性生殖生理和计划生育研究提供了重要的基础数据。

Cell kinetic parameters of K-562 leukemic cells were investigated in microwell cultures in which growth had been initiated from a single cell. Growth of the total population was studied by direct enumeration, 3H-thymidine labelling and flow cytometry and growth of clonogenic cells studied by replating and3H-thymidine suicide. In 7 days colonies of K-562 cells, the durations of total cell cycle, G1, S, G2 and M phases were 20.8, 3.5, 12.9, 3.3 and 1.1 hours respectively, the growth fraction being 0.92 and cell...

Cell kinetic parameters of K-562 leukemic cells were investigated in microwell cultures in which growth had been initiated from a single cell. Growth of the total population was studied by direct enumeration, 3H-thymidine labelling and flow cytometry and growth of clonogenic cells studied by replating and3H-thymidine suicide. In 7 days colonies of K-562 cells, the durations of total cell cycle, G1, S, G2 and M phases were 20.8, 3.5, 12.9, 3.3 and 1.1 hours respectively, the growth fraction being 0.92 and cell loss factor 0.084.Study of clonal-forming cells by replating indicated that clonogenic cells comprised 40% of the total cells and 3H-thymidine suicide showed that the duration of cell cycle for these cells was 22.5 hours and that of S phase 11.7 hours.

本文测定了由单个细胞生长而来的K-562白血病细胞群体及其克隆形成细胞的细胞周期参数。培养第7天,K-562克隆细胞的细胞周期,G_1期,S期,G_2期及M期分别乃20.8,3.5,12.9,3.3和1.1小时。生长分数为0.92;细胞丢失因素为0.084。经再接种法测定的K-562克隆形成细胞占总细胞的40%,其细胞周期为22.5小时,S期为11.7小时。

 
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