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1)  NIH/3T3 Fibroblast
NIH/3T3成纤维细胞
2)  NIH-3T3 rat fibroblasts
NIH-3T3小鼠成纤维细胞
3)  rat fibroblast line NIH-3T3
鼠成纤维细胞株NIH-3T3
1.
Objective To construct eukaryotic green fluorescent protein expression vector 1(pEGFP-N1) of human growth hormone releasing hormone receptor splice variant type 1(GHRHR-SVT1) gene and Its expression in rat fibroblast line NIH-3T3 cells.
目的构建人生长激素释放激素变异受体1型(GHRHR-SVT1)基因绿色荧光蛋白真核表达载体1(pEG-FP-N1)并在鼠成纤维细胞株NIH-3T3细胞中的表达。
4)  NIH 3T3 cells
NIH 3T3细胞
1.
Construction of pLNCX/anti-CD20scFv/IgGFc/CD80/CD28/ζ eukaryotic expression vector and expression in NIH 3T3 cells;
真核表达载体pLNCX/anti-CD20scFv/IgGFc/CD80/CD28/ζ的构建及其在NIH 3T3细胞株中的表达
2.
Objective To establish a cytoplasmic M-CSF-stably-expressing cell line, and to explore the effect of cytoplasmic M-CSF on the proliferation and mobility of NIH 3T3 cells.
方法:PCR分别扩增人M-CSF的胞外活性区和功能区,连接到胞浆定位载体pCMV/cyto/myc质粒,得重组质粒pCMV/cyto/myc-h-M-CSF,再将重组质粒稳定转染NIH 3T3细胞,得到分别稳定表达M-CSF的胞外活性区和功能区的细胞株。
5)  NIH 3T3 cell
NIH 3T3细胞
1.
To investigate the expression of Nogo-A and srGAPs in NIH 3T3 cells, Western blot analysis was performed to verify protein expression of Nogo-A and demonstrated specific Nogo-A bands at about 230 kD on NIH 3T3 cell extracts.
为检测Nogo-A和srGAPs蛋白在NIH 3T3细胞上的表达,应用Western印迹的方法检测Nogo-A蛋白的表达。
2.
Methods Plasmid containing the human PDGFR-β gene was constructed and stably transfected into the mouse NIH 3T3 cells,followed by the functional analysis of the transfected clone cells.
1-PDGFR-β,将其转染至NIH 3T3细胞,获得稳定转染的细胞克隆,并对其进行功能学鉴定及应用;应用瞬时转染PDGFR-β的HeLa细胞,建立PDGF依赖性的受体磷酸化细胞模型。
6)  NIH/3T3 cells
NIH/3T3细胞
1.
Preliminary study of mechanism on a novel gene pp3774 inhibiting NIH/3T3 cells growth;
新基因pp3774抑制NIH/3T3细胞生长机制初探
2.
Acute cytotoxicity of alternariol on NIH/3T3 cells
互隔交链孢酚对NIH/3T3细胞的急性毒性作用
3.
ObjectivesTo investigate the effects of a new houttnin derivative(NHD) on cell proliferation and expression of syndecan-4 protein in rat VSMCs and NIH/3T3 cells induced by TNF-αin vitro.
研究目的本课题以抗炎活性单体鱼腥草素经结构改造后获得的一种低毒高效的新型鱼腥草素衍生物(new houttnin derivative,NHD)为观察对象,通过建立体外细胞培养模型,了解NHD对TNF-α诱导的大鼠VSMCs及NIH/3T3细胞的增殖和syndecan-4蛋白表达的影响,争取获得其新的生物活性,为拓宽NHD的临床应用范围提供相关的实验依据。
补充资料:碳(石墨)纤维增强体(见碳纤维、石墨纤维)


碳(石墨)纤维增强体(见碳纤维、石墨纤维)
earbon(graPhite)fibrereinforeements

,、、里z耽维增强体earbon(graphi现inforcements用于复合材料中承受负荷,田的磷纤始知五史纤俯亡e)fibre起增强作
说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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