首页> 外文期刊>In Vitro Cellular & Developmental Biology - Animal >Serum-free culture of an embryonic cell line from Bombyx mori and reinforcement of susceptibility of a recombinant BmNPV by cooling
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Serum-free culture of an embryonic cell line from Bombyx mori and reinforcement of susceptibility of a recombinant BmNPV by cooling

机译:家蚕胚胎细胞系的无血清培养和通过冷却增强重组BmNPV的敏感性

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摘要

We established the first continuous cell line that uses a serum-free culture from the embryo of Bombyx mori (Lepidoptera: Bombycidae), designated as NIAS-Bm-Ke17. This cell line was serially subcultured in the SH-Ke-117 medium. The cells adhere weakly to the culture flask, and most cells have an oval shape. The cell line was subcultured 154 times, and the population doubling time is 83.67 ± 5.22 h. Random amplification of polymorphic DNA-polymerase chain reaction with a tenmar single primer for discrimination of insect cell lines recognized the NIAS-Bm-Ke1 cell line as B. mori. This cell line does not support the growth of the B. mori nuclear polyhedrosis virus (BmNPV) in the absence of the heat-inactivated hemolymph of B. mori. However, the heat-inactivated hemolymph in 1% volume of the medium supported a high level of susceptibility to BmNPV. In addition, the cooling treatment of the cells at 2.5°C also enhanced the susceptibility. We report a new serum-free culture system of the B. mori cell line for the baculovirus expression vector system.
机译:我们建立了第一个使用来自家蚕(鳞翅目:家蚕)胚胎的无血清培养物的连续细胞系,命名为NIAS-Bm-Ke17。该细胞系在SH-Ke-117培养基中连续传代培养。细胞与培养瓶的粘附力很弱,大多数细胞呈椭圆形。将细胞系传代培养154次,群体倍增时间为83.67±5.22h。用tenmar单一引物对昆虫细胞系进行鉴别的多态性DNA聚合酶链反应的随机扩增将NIAS-Bm-Ke1细胞系识别为桑蚕。在没有热灭活家蚕血淋巴的情况下,该细胞系不支持家蚕肠核多角体病毒(BmNPV)的生长。但是,在1%体积的培养基中,热灭活的淋巴液对BmNPV的敏感性较高。另外,在2.5℃下对电池进行冷却处理也增强了磁化率。我们报告杆状病毒表达载体系统的桑蚕细胞系的新的无血清培养系统。

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