1) NIH method
NIH法
1.
Its result was conformed by animal NIH method.
以传统的动物NIH法对电泳结果进行验证,实验结果显示该方法特异、重复性好、简便易行,与NIH法有较好的相关性。
2.
The determination results of 20 batches of virus bulks and prepared vaccines by the developed method showed no significant differences with those by NIH method.
97;批间及试验内变异系数均小于10%,特异性、稳定性均良好;检测20批病毒原液毒力及疫苗效力,结果与NIH法相比,差异无统计学意义。
2) NIH assay
NIH法
1.
Methods: The samples of rabies vaccine were tested by NIH assay for potency and Sandwich ELISA for G glycoprotein.
目的:用单克隆抗体制备的双抗夹心ELISA法,快速检测人用狂犬病疫苗中的狂犬病毒糖蛋白G的含量,并探讨其替代NIH法的可行性。
4) NIH-CPSI score
NIH-CPSI评分
5) 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。
6) 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。
补充资料：法性属法为法性土
【法性属法为法性土】
谓真如法性之理，譬如虚空，遍一切处，乃是法身所证之体，即为所依之土，故名法性属法，为法性土。
谓真如法性之理，譬如虚空，遍一切处，乃是法身所证之体，即为所依之土，故名法性属法，为法性土。
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