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Isolation、Identification and Sequence Analysis of Differential Expressed Genes Induced by IL-1β in NIT-1 Pancreatic β-Cells
中文意思:
IL-1β诱导后NIT-1胰岛β细胞差异表达基因的分离、监定和序列分析


以下为相关句子列表(点击查看,可以看对应的解释):
Isolation, Expression and Function Analysis of Stress-related Genes in Plants 植物逆境相关基因的克隆、表达及功能分析
Isolation, Pure Cultivation and Total DNA Extraction of Microcystis aeruginosa Kütz in Dianchi Lake 滇池铜绿微囊藻(M.aeruginosa Ktz)的分离培养与总DNA提取的改进
Isolation, culture and identification of human pancreatic stem cells and their differentiation characteristics in vitro 人胰腺干细胞的体外分离培养、鉴定和分化特性
Isolation,cultivation and identification of chicken embryonic stem cells 鸡胚胎干细胞的分离、培养和鉴定
Isolation,culture and identification of murine embryonic stem cells of Kunming species 昆明种系小鼠胚胎干细胞的分离培养及特性鉴定
Isolation、Identification and Sequence Analysis of Differential Expressed Genes Induced by IL-1β in NIT-1 Pancreatic β-Cells IL-1β诱导后NIT-1胰岛β细胞差异表达基因的分离、监定和序列分析
It indicate that the insecticidal protein in the supernatant is thermal instable, which corresponding with the property of Vip3A protein. 这说明上清蛋白含有一种对夜蛾科有高毒力和热不稳定性的蛋白,这与Vip3A蛋白的性质一致,从而确立了这种检测和鉴定方法的可行性。
It is resulted that the percentage of supercoiled pUDKH in plasmid is more than 95%,and RNA undetected. The content of host protein remained is 0.0166 u g/mg and chDNA is less than 2ng/mg,endotoxin is 0.00178EU/mg. 结果表明:质粒中超螺旋pUDKH含量达95%(质量百分比)以上,残留核糖核酸RNA检测不到,宿主蛋白含量小于10mg/mg质粒DNA,残留宿主DNA含量小于2ng/mg质粒DNA,内毒素含量约0.00178EU/mg。
It is showed that the cell parameters increased with Zr~(4+)increasing and KTP octahedron crystal was badly distorted. 随着掺杂Zr~(4+)浓度的增加,晶胞参数明显增大,KTP中八面体畸变的程度会更高。
It means that the two genes, ETV5 and DKFZ, may be involved in the cell proliferation. 推测ETV5、DKFZ两个基因可能与细胞的增殖相关。
It showed BL21(DE3) was the better bacterial host. The method of pH-stat fed-batch culture was applied to obtain high cell density. The final cell density OD600 of grown pNS2/BL21(DE3) was 71.64 and the volumetric productivity was 0.8g/L. 研究了重组质粒pNS2在两种宿主菌中的摇瓶与10L发酵罐培养表达情况,确定了较适的宿主菌为BL21(DE3),采用pH-stat补料分批发酵,工程菌pNS2/BL21(DE3)最终菌体密度OD_(600)达71.64,表达量为0.8g/L。
 
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