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At present, Our main products are fish, shrimp, crab, shellfish four main categories, a total of more than 30 varieties; products are freeze-led South American carinicauda series products, such as shrimp to take the lead in to the first shrimp, butterfly shrimp, Fissidens shrimp, shrimp; frozen shellfish products, where mussels, shellfish, clams string, semi-shell clams, whole clam meat; frozen tilapia products, such as the original article tilapia, second to tilapia , Tilapia Fillet; frozen squid products, such as the original article squid, squid torso, squid ring, squid slice; frozen cut crab block, frozen fillets, such as horse face.

目前,公司主要产品有鱼、虾、蟹、贝四大类,共30多个品种;主导产品有冻南美白虾系列产品,如带头虾、去头虾、蝴蝶虾、凤尾虾、虾仁;冻贝类系列产品,如有青口贝、文蛤串、半壳文蛤、全肉文蛤;冻罗非鱼系列产品,如原条罗非鱼、二去罗非鱼、罗非鱼片;冻鱿鱼系列产品,如原条鱿鱼,鱿鱼胴,鱿鱼圈,鱿鱼片;冻切蟹块,冻马面鱼片等。

High frequencies of solitary snails, slender shell morphology, small females and low fecundities were character of snails on the branching Porites.

在分枝状微孔珊瑚上的紫口珊瑚螺大部分单独存在、个体大小变异较小且比例上壳的形态较窄、雌螺较小且总卵鞘面积较小。

Chang Ching-Hsieh says," now hardcover books published more and more, but there are some unique hardcover book is important to note the problem, such as book Groove of the deep and narrow widths, type could not be opened and the mouth of the superstandard, the impact on the quality of the book."

张庆连说,&现在精装书出版越来越多,但精装书有些特有的问题值得注意,如书槽深浅宽窄度不一、书壳打不开、飘口超标等问题,影响了图书的质量&。

The structure brief introduction the dense thick liquid pump of one stud of i-1b s series is formed by four parts electromotor , shaft coupling , pump and bases motive force joining in marriage usefulness uses y s series asynchronous electromotor of three-phase the shaft coupling uses the water pump with the paw mould elasticity shaft coupling the pump by the pump shell , become hollow inside axle and universal twists joints and winds axle , stud , bush and axle seal and package places and goes out the material mouth etc and forms , and the section of stud is the oval for round and bush section , and his interior surface is the duplexing spirals faces .

结构简介 i-1b系列单螺杆浓浆泵由电动机、联轴器、泵和底座四个部分组成。配用的动力采用y系列三相异步电动机。联轴器采用水泵用爪型弹性联轴器。泵由泵壳、空心轴、万向绞接头、绕轴、螺杆、衬套、轴封装置和出料口等组成,螺杆的断面为圆形、衬套断面为椭圆形,其内表面为双螺旋面。

On the crucible salt bath's furnace shell is loaded with the circular upper hood, the crown has the air vent to put

坩锅盐浴炉的炉壳上部装有圆形上罩,顶部有排气口可接通风系统,以排除有害气体,上罩下

On the crucible salt bath's furnace shell is loaded with the circular upper hood, the crown has the air vent to put through the wind system series, removes the noxious gas, lower part the upper hood has the cover gate which and the port hole two leaves may rotate.

坩锅盐浴炉的炉壳上部装有圆形上罩,顶部有排气口可接通风系统,以排除有害气体,上罩下部有两扇可转动的罩门和观察孔。

On the crucible salt bath's furnace shell is loaded with the circular

坩锅盐浴炉的炉壳上部装有圆形上罩,顶部有排气口可接通风系统,以排除有害气体,上罩下

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。

The pump rotor shaft and motor are installed vertically, pump inlet at the top of the lower part of the exhaust port at the pump, pump casing with a water-cooled units, to reduce the pump bearings and seal at the temperature.

泵的转子轴及电机均为竖直安装,泵进气口在上面,排气口在泵下部,泵壳带有水冷套,以降低泵轴承及轴封处的温度。

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