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The product is extracted from the plant to a natural-fire factor, in a sterile vacuum workshop deployment.

该产品主要是从植物中提炼出一种纯天然清火因子,在无菌真空车间进行调配。

Can improve the survival ratio of seeding. Culturing in hormone media can make meristem tip survive once time, and the result is better than two-time-cultivation.3、The meristem tip with two phyllomes(0.3-0.4mm in size)were found to suitable for virus-free seeding culture that were cut from aseptic seeding, which led to higher survival and virus-free ratio, up to 72.1%and 54.2%.

在培养基中添加椰汁、香蕉汁等有机添加物可以明显提高成苗率。3、采用二次剥离茎尖的方法,从无菌试管苗上切取带2个叶原基(大小0.3-0.4mm)茎尖分生组织培养,成苗率为72.1%,脱毒率为54.2%。

When cultures are grown without phages or under aseptic conditions, they lose their phage resistance.

当培养物存在于没有噬菌体或无菌的条件时,它们便失去了抵抗噬菌体的能力。

In addition, neutrophils from mice that were raised in a germ-free environment or on antibiotics were likewise diminished in their immune responses, but this effect was not permanent: Re-exposure of these mice to a conventional environment (that is, one containing normal bacteria) restored immune function.

并且,在无菌条件下或者使用抗生素条件下的中性粒细胞升高,都伴随着免疫反应的降低。但这种效果并不是永久的:将小鼠重新暴露于含有正常细菌的正常环境中可以使其恢复免疫功能。

Store at a temperature between 2 and 25 in a sterile well-closed container, unless it is intended for immediate use.

如果不立刻使用,则在2 到25 之间以无菌且密闭良好的容器保存。

Regarding fruit processing, JUMP have mastered his own competitive technology from fruit receiving, pre-treatment, vacuum evaporating to tube in tube sterilization and aseptic filling.

在番茄酱及其他果汁果酱加工项目上,我司通过与意大利伙伴公司的全面技术合作,现在在前果处理、冷破工艺、多效节能浓缩、套管式杀菌和无菌大袋罐装等方面已取得国内企业无法比拟的技术优势。

The recombinant plasmid pBI121-VP6 was transformed into Agrobacterium tumefaciens strainLBA4404 by freeze-thawing method and the introduced into the sterile tube culture shoot of tobacco NC89 and baoding alfalfa by leaf disc infection method.

以冻融法将pBI121-VP6重组质粒导入根癌衣杆菌LBA4404,用叶盘法转化于NC89烟草和保定紫花苜蓿的无菌试管苗。

PHap1 was first transformed into Agrobacterium tumefaciens strain LBA4404 by electroporation first and then introduced into the sterile tube culture seedlings of different susceptible potato eultivars'Mira','Zhong-5-1'and'Jinguan', and tobacco cultivar NC89, respectively, by the leaf disc infection method.

以电激法将pHap1导入根癌农杆菌LBA4404,用叶盘法分别转化马铃薯青枯病感病品种米拉、中-5-1、金冠以及烟草感病品种NC89的无菌试管苗。

METHODS: Human AMSCs were isolated in vitro sterilely. At the third passage, 0.5 mL single cell suspension at 1×109/L was obtained and transplanted by tail venous pathway in transplantation group mice, Mice in the control group were injected with an equal volume of saline. APP-gene mice in the normal group were left intact. 5'-bromo-2-deoxyuridine labeled third-generation AMSCs expression was detected in mice brain tissue by immunohistochemical method.

无菌条件下体外分离培养人羊膜间充质干细胞,传至第3代将细胞浓度调整为1×109 L-1,经尾静脉注入0.5 mL至细胞移植组转APP+基因小鼠体内;对照组经尾静脉注入同体积的生理盐水;正常组转APP-基因小鼠不给予任何干预措施。

The mice in experimental group and control group were exposed to 350 cGy radiation produced by 60Co. After 3 h, karyocytes at different concentrations in the fresh human umbilical cord blood were injected into the mice in experimental group A, B, C via their tail veins, and the equal volume of normal sodium was also injected into control group via tail veins. After one month, carbon tetrachloride (CCl4) was injected into experimental group A, B and control group via abdominal cavity, and the equal volume of normal sodium was injected into experimental group C. After two months, immunohistochemistry and reverse transcriptase polymerase chain reaction were used to detect the expressions of human cytokeratin-18 (CK18), cytokeratin-19 (CK19) and albumin in liver tissues of all mice.

采用60Co治疗仪γ射线对实验组和对照组行350cGy的亚致死剂量照射,实验组A、B、C3组照射后3h内经尾静脉分别输入1.0×10^7个/只、2.0×10^7个/只和3.0×l0^7个/只人新鲜脐血有核细胞,对照组经尾静脉注入等体积无菌生理盐水。1个月后对实验A、B组和对照组裸鼠经腹膜腔注射四氯化碳(CCl4),实验C组注射等体积生理盐水。2个月后采用免疫组化和RT-PCR方法检测裸鼠肝组织人源性CK18、CK19和人源性白蛋白的表达。

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