1) bipartite nuclear localization signal
双组分核定位信号
2) NLS
核定位信号
1.
BACKGROUND & AIM:To analyze the exogenous expression and localization of hNRDRA2 in eukaryocyte and demonstrate the function of the predicted nuclear localization signal(NLS).
背景与目的:研究hNRDRA2在真核细胞中的定位情况,并验证其羧基端预测的核定位信号(NLS)是否能引导蛋白核输入。
2.
Some basic nuclear localization signals(NLS) have the capability of penetrating cell membrane and deliverying recombinant proteins, DNA, oligonucleotide into living cells.
一些核定位信号肽 (NLS)具有通透生物膜和携带外源蛋白质、DNA、寡核苷酸等进入细胞的能力。
3.
According to the PredictNLS prediction, twelve different fragments of EGFP/Si1 recombinants were constructed to identify precise NLS regulation sequence.
通过构建不同长度的EGFP/Si1基因突变体观察其核定位信号所在区段,发现核定位信号区在465～531氨基酸残基之间。
3) nuclear localization signal
核定位信号
1.
Progress in utilizing nuclear localization signal peptides in gene transfer;
核定位信号肽用于基因转移的研究进展
2.
Biomedical application of nuclear localization signal peptides
核定位信号类短肽的生物医学应用
4) nuclear localization signal(NLS)
核定位信号
1.
Following stimulation, NF κB and IκB import into nucleus through nuclear pore complexes(NPC),mediated by nuclear localization signal(NLS), respectively.
当细胞受到多种外界信号刺激 ,NF κB、IκB分别在核定位信号 (NLS)的介导下经核孔复合物 (NPC)转运入核 。
5) nuclear localization signal (NLS)
核定位信号
1.
To clarify the roles of nuclear localization signal (NLS) in inhibitory effect of HSP70 on H2O2-mediated nucleolar segregation, four eukaryotic vectors pcDNA3.
为探讨核定位信号在热休克蛋白70(HSP70)抑制H2O2所致核仁损伤中的作用,采用分子克隆技术分别构建了4个真核表达载体,pcDNA3。
2.
Objective: To structurally analyse and functionally identify the nuclear localization signal (NLS) in BRD7 and then study its effect on the subcellular localization of BRD7.
本研究旨在对BRD7的核定位信号进行预测、结构分析和功能鉴定,并考察其对BRD7亚细胞定位的影响。
6) nuclear localization signal sequence
核定位信号序列
1.
To identify nuclear localization signal sequence (NLS) of proline-rich nuclear receptor coregulator protein 1 (PNRC1), vectors expressing green fluorescence protein(GFP)-tagged PNRC1 and GFP-tagged PNRC1 mutant with the putative NLS(aa 94-101, PKKRRKKK) deletion were generated then transfected into mammalian cells.
为鉴定富含脯氨酸核受体辅调节蛋白1(PNRC1)分子的核定位信号序列(nuclear localization signal sequence ,NLS) ,在生物信息学方法预测的基础上,先构建野生型PNRC1及删除预测NLS的PNRC1突变体的绿色荧光蛋白(GFP)重组表达载体,转染细胞后通过激光共聚焦显微镜观察PNRC1分子在删除预测NLS后细胞内的定位变化。
补充资料：异性双位配位体
分子式：
CAS号：
性质：又称异性双位配位体。即含有两种不同原子作为配位原子可分别与中心原子成键的配体。如NO2-，在M-O-N＝O中配体为亚硝酸根，是以氧配位。在M-NO2中配体为硝基，是以氮配位。CN-(氰根)，NC-(异氰根)，SCN-(硫氰酸根)，NCS-(异硫氰酸根)等都是两可配位体。
CAS号：
性质：又称异性双位配位体。即含有两种不同原子作为配位原子可分别与中心原子成键的配体。如NO2-，在M-O-N＝O中配体为亚硝酸根，是以氧配位。在M-NO2中配体为硝基，是以氮配位。CN-(氰根)，NC-(异氰根)，SCN-(硫氰酸根)，NCS-(异硫氰酸根)等都是两可配位体。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条