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acetylate相关的网络例句

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与 acetylate 相关的网络例句 [注:此内容来源于网络,仅供参考]

Fluorescent labeling acetylate Dil-Ac-LDL method was used to identification.

采用荧光标记乙酰化Dil-Ac-LDL的方法鉴定。

This thesis studies biodegradable materials which are made from modified soybean protein isolate by acetylate and glycerin.

研究大豆分离蛋白经过乙酸酐改性,甘油增塑之后制取可生物降解材料。

Study on the quantum chemical calculations is performed by means of MNDO method on VAX8350 computer for rubescensine A and its acetylate derivative.

本文用MNDO方法在VAX8350计算机上对冬凌草甲素及其乙酰衍生物进行了量子化学计算研究。

Use fluorescent labeling acetylate Dil-Ac-LDL method to identify the cells.

结果:①成功培养大鼠心肌微血管内皮细胞,用荧光标记乙酰化Dil-Ac-LDL的方法鉴定为微血管内皮细胞。

SAGA is a multifunctional ATP=independent chromatin remodeling complex which is composed of at least 20 proteins. It can acetylate N=terminal lysines of nucleosomal histone H3 and H2B to loose chromatin structure and promote transcription initiation.

SAGA是一个至少由20个蛋白组成的不依赖ATP的多功能染色质重塑复合物,它通过对组蛋白H3和H2B氨基末端赖氨酸乙酰化修饰来松动染色质结构,从而促进基因转录的起始。

In chromatin immunoprecipitation assay, we found that CBP/p300 could acetylate histones on IL-5 promoter, resulting in increased accessibility of the open chromatin to the transcriptional machinery and therefore promoted gene transcription.

这样产生一个相对开放的染色质构型,从而促进转录机器与DNA的结合,进而促进转录。

Since CBP can acetylate histone H3 and histone H4 and interact with Zta, we examined the possibility that CBP-Zta complex localizes on oriLyt and facilitates EBV genome replication upon viral reactivation by causing chromatin remodeling around oriLyt.

由於CBP可乙醯化组蛋白H3与组蛋白H4,且CBP可与Zta相互作用,因此我们探讨在EB病毒活化后,CBP是否会经由与Zta结合而座於oriLyt上,并改变oriLyt附近的染色质结构,进而有助於病毒DNA的复制。

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This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。

There is no differences of cell proliferation vitality between labeled and unlabeled NSCs.

双标记神经干细胞的增殖、分化活力与未标记神经干细胞相比无改变。