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牛疫

与 牛疫 相关的网络例句 [注:此内容来源于网络,仅供参考]

FMD is a virulent infectious disease caused by FMDV that infects artiodactyl such as cattle, sheep, pig, et al. Outbreak and prevalence of the disease endanger the good development of graziery seriously and cause great financial loss, so all the world highlight study and contol of the disease.

口蹄疫(Foot-and-Mouth Disease,FMD)是由口蹄疫病毒(Foot-and-Mouth Disease Virus,FMDV)引起的牛、羊、猪等偶蹄动物感染的一种烈性传染病,该病的发生和流行严重危害畜牧业的健康持续发展,造成巨大的经济损失,因此世界各国相当重视对该病的研究和防治。

FMD is a virulent infectious disease caused by FMDV that infects artiodactyl such as cattle, sheep,pig, et al. Outbreak and prevalence of the disease endanger the good development of graziery seriouslyand cause great financial loss, so all the world highlight study and contol of the disease. Material of the study was FMDV from cell culture.

口蹄疫(Foot-and-Mouth Disease,FMD)是由口蹄疫病毒(Foot-and-Mouth Disease Virus,FMDV)引起的牛、羊、猪等偶蹄动物感染的一种烈性传染病,该病的发生和流行严重危害畜牧业的健康持续发展,造成巨大的经济损失,因此世界各国相当重视对该病的研究和防制。

Foot-and-mouth disease affects animals with cloven hooves, such as cattle, pigs, deer, goats and sheep.

口蹄疫可以传染到相近的一些蹄类动物,比如牛、猪、鹿、山羊和绵羊。

The plant Quarantine Lab had intercepted more than 200 quarantine pests such as : Tilletia indica , Tilletia controversa , Bursaphelenchus xylophilus , sorghum halepense , Acanthoscelides obtectus , Sternochetes mangiferae , Bactrocera dorsalis , Coptoermes curvignathus for nearly 5000 batches ; The Animal Quanantine Lab had intercepted about 20 cow which had some pathogens evidence of infectious disease such as : bovine infectiouse rhinotracheitis , leukaemia bovum , paratuberculosis and so on ; The food microorganism lab had detected over 300 unqualified products such as Salm-Sury , Listeria monocytogenes , Mycobacterium paratuberculosis etc .

多年来,分中心各实验室切实履行严格把关的职责,植物检疫共截获大豆疫霉病菌、小麦印度腥黑穗病菌、小麦矮腥黑穗病菌、松材线虫、假高梁、菜豆象、芒果果核象甲、桔小实蝇、大家白蚁等国家禁止进境的危险性有害生物220 多种近10000 批次;动物检疫发现感染牛传染性鼻气管炎、牛白血病、副结核等传染病的疫牛20 多头;食品微生物检测共检测沙门、单增、副结核的不合格商品300 多批;分子生物学实验室为国内企业出具非转基因证书和不含有牛羊源成分证书50 余份,使相关的产品能够顺利出口到欧盟、韩国和日本等国。

Common cattle infected with foot-and-mouth virus can be generated by the corresponding bovine antibodies are of no use to humanity, mankind is not cloven-hoofed animals.

牛常见的口蹄疫是病毒感染,可牛产生的相应抗体对人类却毫无用处,人类可不属偶蹄类动物。

Foot-and-Mouth Disease is a severe disease, caused by foot-and-mouth disease virus, of cloven-hoofed animals, particularly swine, cattle and sheep. FMD seriously impair healthy development of animal husbandry and result in considerable economic losses.Therefore, all the countries of the world pay much attention to its study and prevention.

口蹄疫(Foot-and-Mouth Disease,FMD)是由口蹄疫病毒(Foot-and-Mouth Disease Virus,FMDV)引起的牛、羊、猪等偶蹄动物感染的一种烈性传染病,该病的发生和流行严重危害畜牧业的健康持续发展,造成巨大的经济损失,因此世界各国相当重视对该病的研究和防制。

Foot-and-mouth disease virus causes a highly contagious disease which is foot-and-mouth disease in cloven-hoofed animals.

口蹄疫病毒(Foot-and-mouth disease virus FMDV)主要引起牛、猪、羊等偶蹄动物的口蹄疫(Foot-and-mouth disease,FMD)。

Foot and Mouth Disease, a major threat to cloven-hoofed animals such as bovine, swine and sheep, is a highly contagious disease caused by Foot and Mouth Disease Virus. Since it has a high incidence and can easily cause an epidemic outbreak and enormous loss of economy, Office International des Epizooties ranks it in the first in all contagious diseases for domestic animals.

口蹄疫(Foot and mouth disease, FMD)是由口蹄疫病毒引起的主要危害牛、猪、羊等偶蹄动物的烈性传染病,发病率高,传染性强,并能形成国际大流行,国际兽疫局将其排在A类家畜传染病的首位。

By use of site mutation strategy and PCR technology, we obtained the gene P12X3C that includes full length P1, 2A, 3C and a part of 2B and 3B and the gene P12X3C3D that includes full length P1, 2A, 3C, 3D and a part of 2B and 3B. After being digested by restriction enzyme respectively, the gene P12X3C and the gene P12X3C3D were cloned into the pcDNA3. 1 and pTARGET expression vector that were digested by the same enzyme. Recombinant plasmids were checked by restriction enzyme analysis and nucleic acid sequencing. Further more, recombinant plasmids were transfected into BHK-21 cells by using lipoid. The proteins of foot-and-mouth disease virus , which were expressed in BHK-21 cells, were confirmed by sandwich-ELISA and fluoroscopy, and the capsid of FMDV was tested by electron microscope. In order to evaluate enhanced immune response of guinea pigs against FMDV, DNA vaccines which were designed to produce viral capsids lacking infectious viral nucleic acid and contained the gene P12X3C and the gene P12X3C3D were injected respectively with FMDV 3D protein which was expressed in Pichia Pastoris Secreted expression System and purified or with pcDNA3. 1/IFN which includes the gene IFN-α of cattle. Subsequently, Recombinant plasmids were injected to cattles with or without pcDNA3. 1/IFN. Anti-FMDV antibodies were detected by ELISA, and the T lymphocyte proliferation response was tested by MTT assay, neutralization antibodies titers were analyzed by micro-neutralization assay.

为研制带有O型口蹄疫病毒(Foot-and-Mouth Disease Virus,FMDV)China99株结构蛋白基因及多个非结构蛋白基因的DNA疫苗,本研究通过定点突变方法和PCR扩增方法,获得包含有FMDV China99株结构蛋白P1、非结构蛋白2A、3C以及部分2B、3B编码基因的片段P12X3C和包含有FMDV China99株结构蛋白P1、非结构蛋白2A、3C、3D以及部分2B、3B编码基因的片段P12X3C3D,将获得的基因片段直接/酶切后与同样处理的真核表达质粒连接,分别得到重组质粒pcDNA3.1/P12X3C和pcDNA3.1/P12X3C3D、pTARGET/P12X3C3D;对重组质粒进行序列测定、分析,并将重组质粒分别转染BHK-21细胞,通过双抗体夹心ELISA方法和间接免疫荧光标记方法检测细胞中FMDV抗原的表达,用电子显微镜观察病毒空衣壳的组装;为评价重组质粒作为DNA疫苗对实验动物及本动物的免疫效果,将重组质粒经肌肉注射方法接种豚鼠,并与酵母表达的纯化FMDV China99株3D蛋白及带有牛α干扰素的真核表达质粒pcDNA3.1/IFN分别/同时免疫,第二次免疫后第三周豚鼠攻以1OOID〓或1000ID〓的O型FMDV China99株;随后将质粒pcDNA3.1/P12X3C、pcDNA3.1/P12X3C3D与带有牛α干扰素的真核表达质粒pcDNA3.1/IFN同时免疫牛,三周后经牛舌皮攻以10〓ID〓的O型FMDV China99株。

By use of site mutation strategy and PCR technology, we obtained the gene P12X3C that includes full length PI, 2A, 3C and a part of 2B and 3B and the gene P12X3C3D that includes full length PI, 2A, 3C, 3D and a part of 2B and 3B. After being digested by restriction enzyme respectively, the gene P12X3C and the gene P12X3C3D were cloned into the pcDNA3.1 and pTARGET expression vector that were digested by the same enzyme. Recombinant plasmids were checked by restriction enzyme analysis and nucleic acid sequencing. Further more, recombinant plasmids were transfected into BHK-21 cells by using lipoid. The proteins of foot-and-mouth disease virus, which were expressed in BHK-21 cells, were confirmed by sandwich-ELlSA and fluoroscopy, and the capsid of FMDV was tested by electron microscope. In order to evaluate enhanced immune response of guinea pigs against FMDV, DNA vaccines which were designed to produce viral capsids lacking infectious viral nucleic acid and contained the gene P12X3C and the gene P 12X3C3D were injected respectively with FMDV 3D protein which was expressed in Pichia Pastoris Secreted expression System and purified or with pcDNA3.1/lFN which includes the gene IFN-a of cattle. Subsequently, Recombinant plasmids were injected to catties with or without pcDNA3.1/IFN. Anti-FMDV antibodies were detected by ELISA, and the T lymphocyte proliferation response was tested by MTT assay, neutralization antibodies liters were analyzed by micro-neutralization assay.

为研制带有O型口蹄疫病毒(Foot-and-Mouth Disease Virus,FMDV)China99株结构蛋白基因及多个非结构蛋白基因的DNA疫曲,本研究通过定点突变方法和PCR扩增方法,获得包含有FMDV China99株结构蛋白P1、非结构蛋白2A、3C以及部分2B、3B编码基因的片段P12X3C和包含有FMDV China99株结构蛋白P1、非结构蛋白2A、3C、3D以及部分2B、3B编码基因的片段P12X3C3D,将获得的基因片段直接/酶切后与同样处理的真核表达质粒连接,分别得到重组质粒pcDNA3.1/P12X3C和pcDNA3.1/P12X3C3D、pTARGET/P12X3C3D;对重组质粒进行序列测定、分析,并将重组质粒分别转染BHK-21细胞,通过双抗体夹心ELISA方法和间接免疫荧光标记方法检测细胞中FMDV抗原的表达,用电子显微镜观察病毒空衣壳的组装;为评价重组质粒作为DNA疫苗对实验动物及本动物的免疫效果,将重组质粒经肌肉注射方法接种豚鼠,并与酵母表达的纯化FMDV China99株3D蛋白及带有牛α干扰素的真核表达质粒pcDNA3.1/IFN分别/同时免疫,第二次免疫后第三周豚鼠攻以100ID_(50)或1000ID_(50)的O型FMDV China99株:随后将质粒pcDNA3.1/P12X3C、pcDNA3.1/P12X3C3D与带有牛α干扰素的真核表达质粒pcDNA3.1/IFN同时免疫牛,三周后经牛舌皮攻以10~4ID_(50)的O型FMDV China99株。

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随着死亡的吉他手Schuldiner接受主唱的职务,乐队在现实中树立了重要的影响。

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