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supernatant相关的网络例句

查询词典 supernatant

与 supernatant 相关的网络例句 [注:此内容来源于网络,仅供参考]

Methods Culture the odontoblast of healthy and carious teeth, and determine the activities of MMP-2 and MMP-9 in culture supernatant by zymogram.

培养健康牙齿和龋齿成牙本质细胞,利用酶谱分析细胞培养上清中MMP-2和MMP-9的活性。

Methods The subjects were divided into two groups: PIH group (n= 15) and normotensive control group (n=15). Peripheral lymphocytes of the subjucts were separated by Ficoll-Hypaque density centrifugation. The lymphocytes were cultured in RPMI-1640 medium with or without pokeweed mitogen for ten days.Then the supernatant was collected and the IgG and IgM were measured by enzyme linked immunosorbent assay.

采用密度梯度离心法分离妊高征组(15例)和正常妊娠组(15例)的外周血B淋巴细胞,并在有或无美洲商陆有丝分裂原存在的情况下培养10天后,收集上清液,采用酶联免疫吸附试验测定每1×106个B淋巴细胞所分泌的IgG和IgM的量。

Methods CD+4CD45RO+ T lymphocyte subsets were isolated from peripheral blood of patients with bronchial asthma and healthy donors. Then they were cultured with self-B lymphocytes and designated as pokeweed mitogen-stimulated and non-stimulated group. Secreted IgE was measured in the supernatant.

分别分离出支气管哮喘病人及健康对照的CD+4CD45RO+T淋巴细胞亚群,并将其与各自的B淋巴细胞共同培养,设定刺激组及非刺激组,测定培养上清液中IgE的含量。

The in vivo competitive binding test was study by adding the segment protein which CREG most binding to into the supernatant with wt/mCREG receptively. The change of CREG biologic effects on VSMC were analyseses to identified the direct binding of CREG to IGF2R domains.

将与wt/mCREG蛋白高亲合的M6P/IGF2R胞外重组小肽片段分别添加到细胞培养上清中,确定wt/mCREG蛋白对VSMC生物学行为的调控作用(流式细胞分析检测细胞增殖、刮伤实验和明胶酶谱分析细胞迁移能力)是否通过其与M6P/IGF2R小肽的直接亲合作用介导。

SDS-PAGE and Western blot of culture supernatant showed that hsIL-1RⅠ was secretively expressed. Recptor-ligand binding assays showed that the recombinant hsIL-1RⅠ has receptorligand binding activity.

发酵液经SDS-PAGE和Western blot证实分泌表达了sIL-1RI,经蛋白印迹受体配基结合反应证实分泌表达的sIL-1RI具有配基受体结合的生物学活性。

It was more in the sediment than the supernatant fluid.

在沉淀中较在上清中表达得多。

After 30 min of sedimentation, the supernatant was withdrawn for COD and color analysis.

30分钟后,沉淀,上清撤回COD和颜色分析

Results:(1)NSCs form typical neurospheres under adequate concentration in vitro, which are immunoreactive to Vimentin. Typically and terminally differentiated mature neural cells could not be found without the stimulus of mitogen or only under NSCs self-regulation and self-induction;(2)NSCs derived from hippocampus maintain the character of stem cells much longer with better biological behavior; NSCs passed to the 2-3 passage are the best to graft since they have not differentiated;(3)NSCs cultured in vitro could self-regulate and differentiate into neurospheres and progenitors positively immunoreactive to specific antibodies representing neurons, astrocytes, oligodendrocytes and Schwann cells;(4)There are widespread synaptic contacts between various kinds of descendent clones and cells;(5)Neurospheres could be formed without the stimulus of mitogen when NSCs and OECs are cocultured. Many neurospheres and cells immunoreactive to Vimentin, GFAP, MAP2, 02, p75NGFR, GFAP, S-100, Synaptosis, Vimentin, Tau (Tau is only positive in cocultureof HNSCs+HOECs) could be found;(6)The supernatant fluid triturated from adult rat spinal cord stimulates NSCs to differentiate into neurons, but do not terminally differentiate;(7)Fibroblasts and O4 oligodendrocytes are not supported to grow under this culture medium.Part II: Isolation, culture and identification of rat and human olfactory ensheathing cellsOlfactory ensheathing cells/glials are the most powerful cells to enable the regeneration of axons in the central nervous system.

结果表明:①在适宜的浓度体外培养条件下,NSCs能形成典型的神经干细胞克隆球,Vimentin免疫荧光染色阳性,单靠丝裂原刺激或NSCs自我调节和分化诱导,不会产生典型的终末分化的成熟神经细胞;②海马源性的NSCs维持干细胞特性的时间更长,生物学特性更优;③传至第2~3代的NSCs尚未分化时移植最佳;④体外培养的NSCs能自我调控分化为神经元、星形胶质细胞、O2少突胶质细胞、雪旺氏细胞染色阳性克隆球和前体细胞;⑤各种子代克隆球和细胞存在广泛的突触联系;⑥NSCs与OECs联合培养时,不需丝裂原刺激即能形成克隆球,获得大量Vimentin、GFAP、MAP2、O2、p75NGFR、GFAP、S-100、Synaptosis、Vimentin、Tau(Tau只有人HNSCs+HOECs联合培养时出现阳染)染色阳性的克隆球和细胞;⑦脊髓研磨后的上清液刺激神经干细胞向神经元方向分化,但并不出现终末分化;⑧本研究培养条件不利于成纤维细胞、O4生长。

This method was simp le,high sensitive and specific for detecting interleukin 8 in human and rabbit s erum as well as supernatant of cell culture.

该方法是一种简便、灵敏和特异的IL-8分析方法,可用于人和兔血清以及细胞培养上清液中IL-8分析。

Methods Firstly,separated splenetic lymphocytes of BALB/c mice;after cultivation of 72 hours with concanavalin Aand several concentration of(1μM,5μM,10μM)ODN_(A151)or ODN_(1612)(10μM),then detected IFNγand IL-4 in supernatant by ELISA.

方法分离小鼠睥淋巴细胞,根据分组加入伴刀豆蛋白A以及不同浓度的ODN_(A151)或对照的ODN_(1612),培养72 h后采用夹心法ELISA测定上清中的IFN_γ和IL-4浓度。

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我不懂得羞怯和惧怕,我的