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   蛋白 在 畜牧与动物医学 分类中 的翻译结果: 查询用时:0.753秒
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蛋白
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  protein
    The Fusion Protein Gene of Newcastle Disease Virus Strain F_(48)E_8:Sequence Analysis and Expression by a Recombinant Fowlpox Virus
    新城疫病毒F48E8株融合蛋白基因和表达该基因的重组鸡痘病毒
短句来源
    Complete Genomic Sequence of Porcine Reproductive and Respiratory Syndrome Virus Strain CH-1a & Structural and Functional Analyses of lts Envelope Protein
    猪繁殖与呼吸综合征病毒CH-la株基因组解析及其囊膜蛋白结构与功能分析
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    Comparative Study of Meat-type Duck's ldeal Protein Amino Acids Pattern by Different Methods
    不同方法确定肉鸭理想蛋白氨基酸模式的比较研究
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    Study on Cloning and Sequence Analysis and Expression of HN Protein Gene of NDV and Immunogenicity of Recombinant Protein
    新城疫病毒HN蛋白基因的克隆、序列分析、表达及其免疫原性研究
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    Study on Characterization and Function of Chicken Heat Shock Protein 108
    鸡热应激蛋白108特性与功能初步研究
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  albumen
    At 0.002ng/g,0.5ng/g and 20ug/g concentration, the CV% between run was 5.29%, 3.43%, 2.61% for albumen and 5.58%, 3.37%, 1.59% for yolk respectively;
    氯霉素浓度为0.002μg/g、0.5μg/g、20μg/g时蛋白的批间变异系数分别为5.29%、3.43%、2.61%;
短句来源
    On 1 day after the last-administration, the concentrations of CAP in albumen and yolk were 3.61ug/g and 14.51ug/g respectively.
    停药当天,蛋白中的药物含量为3.61μg/g,蛋黄中的药物含量为14.51μg/g;
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    On 5 days of the last administration, the concentrations of CAP in albumen and yolk were 0.05|ig/g and 7.17ng/g respectively.
    停药5d,蛋白中的药物含量为0.05μg/g,蛋黄中的药物含量为7.17μg/g;
短句来源
    2. The Total albumen and Globulin content of serum for trial group were significantly higher than those of control group (P<0 . 05) ;
    2.血液生化指标中,试验组的血清总蛋白和球蛋白含量明显高于对照组(P<0.05);
短句来源
    (2)Decrease supplement feed amount could improve the quantity of egg,40% supplement feed could increase RYCF exceedingly remarkbly (p<0.01), remarkbly increase yolk ratio(p<0.05), and decrease albumen ratio(p<0.05), Yet the Ha-Fu unit remarkbly cuts down (p<0.05) .
    ②降低补料量可以改善蛋品质,40%补料量可以极显著提高蛋黄罗氏比色扇级数(p<0.01),显著提高蛋黄比率(p<0.05),降低蛋白比率(p<0.05),但哈氏单位显著降低(p<0.05)。
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  “蛋白”译为未确定词的双语例句
    Study on Molecular Biology of Egg Drop Syndrome Virus SG9301 Strain and Expression of the Hexon-Encoding Gene
    减蛋综合征病毒四川株(SG9301)的分子生物学及六邻体蛋白基因的克隆和表达的研究
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    Identification and Comparison of Neutralizing Epitopes of Structural Glycoprotein E2 & E~(rns) of Classical Swine Fever Virus Using Phage Display
    应用噬菌体展示技术进行猪瘟病毒结构(糖)蛋白E2和E~(rns)中和抗原表位鉴定和比较
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    The Ontogeny and Expression of Hormone Specified Cells and Their Regulation by Transcription Factor Isl-1 in Adenohypohysis of Chicken Embryo
    鸡胚腺垂体激素特异性细胞的发生及蛋白转录因子Isl-1对其表达的调控性研究
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    Construction and Efficacy of a Recombinant Pseudorabies Virus Expressing GP5 of Porcine Reproductive and Respiratory Syndrome Virus
    表达PRRSV GP5蛋白的重组伪狂犬病毒的构建及其免疫效力的研究
短句来源
    Study on Suicidal DNA Vaccine of Capsid Gene from Swine Vesicular Disease Virus
    猪水疱病病毒衣壳蛋白基因自杀性DNA疫苗研究
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  protein
Polyamines May Modulate Both G Protein-Coupled Receptors and G Proteins
      
Heterodimerization of G-Protein-Coupled Receptors Reveals an Unexpected Level of Pharmacological Diversity
      
The Activation Mechanism of Class-III G-Protein Coupled Receptors
      
Hepatic glutathione, lipid peroxides, glutathione peroxidase, alcohol dehydrogenase, aldehyde dehydrogenase, glycogen and total protein in liver were also significantly altered.
      
3D QSAR STUDIES OF INHIBITORS OF CHOLESTEROL ESTER TRANSFER PROTEIN (CETP) BY CoMFA, CoMSIA AND GFA METHODOLOGIES
      
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  albumen
We analysed CBP in an eider population in the central Baltic Sea 2001-2002, using non-destructive egg albumen sampling combined with protein fingerprinting.
      
Five groups of individually housed albino rats (n=7, initial average weight=48 g) were fed diets based on egg albumen and cornstarch (basal diet 8.2 g Ca, 6.0 g P, 0.7 g Mg, 225 mg Zn, 150 mg Fe, 60 mg Mn, 8 mg Cu, and 5 mg Cd) over a 4-wk period.
      
The albumen of fertile eggs was injected on e-11 with 300 μL of 0.9% saline or 150 μL of serum from e-12 or e-16 chick embryos diluted 1∶1 with saline.
      
Single rapid injections of131I labelled human serum albumen were given into the venous line of the mechanical model and records obtained from collimated scintillation detectors positioned over the heart, lung and brain.
      
Whole blood calcium activity, total plasma calcium, pH, pCO2, and plasma albumen concentrations were measured in ten patients undergoing cardiopulmonary bypass.
      
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1. Temperature adjustment during incubation (Early stage 38.5℃, Midestage 38.0℃, Late stage 37.0℃) showed favorable effect on rate of embryonic development and intensity of nutrient metabolism. The effect of thermo-rise during the early stage was more striking 24 hours after setling of eggs; the experiment group surpassed the controls in rate of development by about one full day, judging from exterior appearance. From the 25th day onward, exterior difference between groups became less manifest, although the...

1. Temperature adjustment during incubation (Early stage 38.5℃, Midestage 38.0℃, Late stage 37.0℃) showed favorable effect on rate of embryonic development and intensity of nutrient metabolism. The effect of thermo-rise during the early stage was more striking 24 hours after setling of eggs; the experiment group surpassed the controls in rate of development by about one full day, judging from exterior appearance. From the 25th day onward, exterior difference between groups became less manifest, although the experimental group pipped the shell earlier with greater strength, emerged early. The newly hatched ducklings were stronger with longer and fuller down, their average initial weight was heavier (47.76 gms as against 46.72 gms for the controls). As a consequence, hatchability was raised by 13.3% (Experimental, 75%, Control, 61.7%). 2. Growth curves of experimental group in length and weight of the embryo and its principal organs such as eye, heart, stomach, intestines, liver, lung, etc, fluctuated above those of the controls, except the heart, during the 25—27th day period only the former fell below the control group, slightly. 3. Manifestations indicating intensive metabolic rate were also in favor of the experimental group. For instance, decreases in egg weight were at faster rate than the control group. Descrepandies between the two groups were especially obvious in the utilization of egg white and egg yolk; egg white of the experimental group was completely utilized from the end of the 20th to the beginning of the 21st day, whereas it was delayed until the end of the 22nd and the beginning of the 23rd day in the controls, As the time of hatching the former had only 4.16 gms. of egg yolk left, while 6.23 gms was still left for the latter. Differences between the number of red blood cells and haemoglobin content were also apparent. 4. Roentgenographic measurements of ossified region taken from the diaphyses of the Humerus and Tibio-fibula likewise proved that the experimental group developed at a faster rate. 5. Sex differentiation was manifest at the 8th day for the experimental group as against the 9th day for the control group.

1.变溫条件(早期38.5℃,中期38.0℃,晚期37.0℃)可以改善胚胎发育的速度和胚体內某些指标变化的影响物质代謝的强度。初期升溫的效果在孵化开始的24小时以后較为明显。試驗組与对照組相比,发育速度一直領先,从外形来看,两組相差1昼夜。而到25昼夜以后,两組外形差別不大,但試驗組啄壳时間早,啄壳强而有力,出雛时間早,初生鴨雛健壮,絨羽长而丰滿,平均体重大(試驗組为47.76克,对照組为46.72克),从而提高了孵化率13.3%(試驗組75%,对照組61.7%) 2.胚胎及其主要器官,如眼、脑、心、胃、腸、肝、肺等长度和重量增长曲綫,試驗組的曲綫一直波动于对照組曲綫的上面,仅在25—27昼夜試驗組略有下降,其中心脏的情况,稍有例外。 3.一些能够說明物质代謝强度的指标,試驗組也一直領先。例如,卵重失重,壳重减重試驗組均快于对照組。特別是卵白、卵黃的利用方面,两組相差更为明显。試驗組在20昼夜末21昼夜初,卵白已被用尽,而对照組却延迟到22昼夜末23昼夜初。到出壳为止試驗組卵黄仅余4.16克,而对照組却还有6.23克。紅血球和血紅蛋白含量,两組差別也很明显。 4.X射綫直接摄影測量肱骨和小腿骨的骨...

1.变溫条件(早期38.5℃,中期38.0℃,晚期37.0℃)可以改善胚胎发育的速度和胚体內某些指标变化的影响物质代謝的强度。初期升溫的效果在孵化开始的24小时以后較为明显。試驗組与对照組相比,发育速度一直領先,从外形来看,两組相差1昼夜。而到25昼夜以后,两組外形差別不大,但試驗組啄壳时間早,啄壳强而有力,出雛时間早,初生鴨雛健壮,絨羽长而丰滿,平均体重大(試驗組为47.76克,对照組为46.72克),从而提高了孵化率13.3%(試驗組75%,对照組61.7%) 2.胚胎及其主要器官,如眼、脑、心、胃、腸、肝、肺等长度和重量增长曲綫,試驗組的曲綫一直波动于对照組曲綫的上面,仅在25—27昼夜試驗組略有下降,其中心脏的情况,稍有例外。 3.一些能够說明物质代謝强度的指标,試驗組也一直領先。例如,卵重失重,壳重减重試驗組均快于对照組。特別是卵白、卵黃的利用方面,两組相差更为明显。試驗組在20昼夜末21昼夜初,卵白已被用尽,而对照組却延迟到22昼夜末23昼夜初。到出壳为止試驗組卵黄仅余4.16克,而对照組却还有6.23克。紅血球和血紅蛋白含量,两組差別也很明显。 4.X射綫直接摄影測量肱骨和小腿骨的骨干骨化区,也証明了試驗組的发育此对照組快。 5.性別分化时間,試驗組在第8昼夜,对照組在第9昼夜。

A simple method for the isolation and purification of ceruloplasmin was described in this paper. An electroimmunodiffusion method used to determine the human serum ceruloplasmin was also reported.The serum ceruloplasmin contents of 178 cases including normal subjects, silicosis suspects, simple silicosis patients in stages Ⅰ, Ⅱ and Ⅲ, and cases of silicosis complicated with tuberculosis in stages Ⅰ to Ⅲ, were estimated with this method.It was found that the serum ceruloplasmin values of patients with silicosis...

A simple method for the isolation and purification of ceruloplasmin was described in this paper. An electroimmunodiffusion method used to determine the human serum ceruloplasmin was also reported.The serum ceruloplasmin contents of 178 cases including normal subjects, silicosis suspects, simple silicosis patients in stages Ⅰ, Ⅱ and Ⅲ, and cases of silicosis complicated with tuberculosis in stages Ⅰ to Ⅲ, were estimated with this method.It was found that the serum ceruloplasmin values of patients with silicosis and silicosis suspects were significantly different from those of normal subjects.

本文报导了一种简单的铜蓝蛋白提纯方法和人血清中铜蓝蛋白的免疫电扩散测定方法,并用此法测定了正常人,疑似矽肺者,Ⅰ、Ⅱ、Ⅲ期单纯矽肺患者及Ⅰ、Ⅱ、Ⅲ期矽肺合并结核患者共178例血清中铜蓝蛋白的含量。发现疑似矽肺和矽肺患者与正常人血清中铜蓝蛋白含量有显著性差异。

Summary The growth requirements of the causal agent of enzootic pneumonia of swine are so fastidious that for seventeen years, since recognizaton of it as an entity by pullar (1948), it had been assumed to be a vitus, until Goodwin and Whittlestone in England, Mare and Switzer in America, near at the same time (1965), could cultivate ie With living cell free media and nominated it as Mycoplasma suipneumonia and M. hyopheumonia respectively. There after, more complex modified media were used to promote facility...

Summary The growth requirements of the causal agent of enzootic pneumonia of swine are so fastidious that for seventeen years, since recognizaton of it as an entity by pullar (1948), it had been assumed to be a vitus, until Goodwin and Whittlestone in England, Mare and Switzer in America, near at the same time (1965), could cultivate ie With living cell free media and nominated it as Mycoplasma suipneumonia and M. hyopheumonia respectively. There after, more complex modified media were used to promote facility for isolation or subcultivation. In recent years, modified Switzer′s medium Jiangsu medium No.2 (KM2), composed of 50% Eagle′s solution, 30% of 1% lactoalbumin hydrolysate, 20% normal swine serum inactivated at 56℃ for 30 minutes, with additional 1% fresh yeast extract, penicillin 500 unit/ml, thallium acetate 0.0125% and Pheol red 0.002% has been widely used in our country for isolation and subcultivation with more satisfactory results as compared With other media. Yet the costive amino-acids and biotic materials and laborious procedure in prepation of fresh yeast extract expensed more money and much time. Hence, we have tried to use Streptococcus pyogenes or Staphylococcus aureus culture preparation as substitute for Eagle′s solution and yeast extract. The procedures are as follows: 1. Martin broth is inoculated with selected pure culture of Streptococcus pyogenes (or Staphylococcus aureus) and incubated in 37℃ for 24 hours. 2. Centrifuge the culture at 2500 R.P.M. for 30 minutes. 3. Filter the supernatant through sterile seitz filter with F.K. disc under the negative pressure not above 25cm. mercury. 4. Grind the precipitated bacterial ceils with silicon carbide to homogeneous pulp, mix with aliquot of the Cultural supernatant, then filter the mixture through the same seitz filter already used. The filtrate is inocuialed in martin broth and agar slant to test the sterility. The sterile filtrate is dispensed to a number of bottles and kept in frozen state ready for use. The experimental results poited out: 1. The components in bactereal filtrate that promote growth of Mycoplasma suipneumonia are heat labile, though not completely damaged by 56℃ for 30 minutes to Streptococcus and 70℃ 30 minutes to Staphylococcus and do not resist autoclave temperature. 2. The beneficial components to growth of M. suipneumonia exsist both in the cultural fluid and bacterial cells. 3. Survival time: in 37℃, KM_2 culture last at 4th day, the cultures of the media with Strptococeus substitute (Str_50) or Staphylococcus substitute (Sa_50) all last at 8th day; in 4-8℃, KM_2 culture last at 12th day, the cultured cf str_50 last at 26th day and the culture of Sa_50 last at 30th day. 4. Once a certain inoculum of M. suipneumonia added to KM_2 did not show growth any more, but could grow in KM_2 containing 10% Streplococcus preparation. This may be a hint that the preparation of Streptococcus might contain some factors possessing the ability of reviving M. suipneumonia at a critical point. 5. There are no visible differences between KM_2, Str_50 and Sa_50 cultures in ceils′ morphology and pathogenicity, but somewhat diversities in growth rate. 6. Martin broth could be used as substiute instead of 1% lactoalbumin hydrolysate soltrion for subcultivation of M. suipneumonia.

一、以50%的化脓性链球菌或黄金色葡萄状球菌的马丁汤培养物的无菌过滤液(包括过滤的菌体微粒)(代号分别为Str和Sa)、30%的1%水解乳蛋白溶液,20%的正常猪血清(56℃灭活30分钟)(附加物如青霉素500单位/毫升,醋酸铊0.0125%,酚红0.002%)组成的液体培养基,酸度校正至pH7.2~7.4,培养猪肺炎支原体,生长良好。也可用作含1.2%高纯度琼脂固体培养基的基础。含50%链球菌液培养基代号为Str_(50),含50%葡萄状球菌的代号为Sa_(50)。二、在生长旺盛后保存于37℃中,Str_(50)及Sa_(50)培养物均存活8天,而KM_2(由50%的Eagle氏液,30%水解乳蛋白溶液,20%灭活正常猪血清,1%酵母抽出液和附加物如青霉素500单位/毫升,醋酸铊0.125%,酚红0.002%组成)的培养物仅存活4天。在4——8℃冰箱中,Str50培养物存活26天,Sa50培养物存活30天,而KM_2培养物仅存活12天。三、供给生长的成份既存于菌液,也存在于菌体。四、供给生长的成份不耐高热蒸汽灭菌。五、链球菌以65℃30分钟灭活,葡萄状球菌以70℃30分钟灭活,生长成...

一、以50%的化脓性链球菌或黄金色葡萄状球菌的马丁汤培养物的无菌过滤液(包括过滤的菌体微粒)(代号分别为Str和Sa)、30%的1%水解乳蛋白溶液,20%的正常猪血清(56℃灭活30分钟)(附加物如青霉素500单位/毫升,醋酸铊0.0125%,酚红0.002%)组成的液体培养基,酸度校正至pH7.2~7.4,培养猪肺炎支原体,生长良好。也可用作含1.2%高纯度琼脂固体培养基的基础。含50%链球菌液培养基代号为Str_(50),含50%葡萄状球菌的代号为Sa_(50)。二、在生长旺盛后保存于37℃中,Str_(50)及Sa_(50)培养物均存活8天,而KM_2(由50%的Eagle氏液,30%水解乳蛋白溶液,20%灭活正常猪血清,1%酵母抽出液和附加物如青霉素500单位/毫升,醋酸铊0.125%,酚红0.002%组成)的培养物仅存活4天。在4——8℃冰箱中,Str50培养物存活26天,Sa50培养物存活30天,而KM_2培养物仅存活12天。三、供给生长的成份既存于菌液,也存在于菌体。四、供给生长的成份不耐高热蒸汽灭菌。五、链球菌以65℃30分钟灭活,葡萄状球菌以70℃30分钟灭活,生长成份尚未完全破坏,但不如未灭活的生长旺盛。六、加10%的Str于KM_2中有促进猪肺炎支原体生长和复苏作用。用于培养棉花拭子深擦病猪喉头和鼻道的滤液,分离率可达77.8%。七、Str_(50)和Sa_(50)制造方法较简单,成本低廉,组成成份容易获得,宜于一般实验室应用和大量生产。八、Sa_(50)中30%的水解乳蛋白溶液可以马丁汤代替,用于接种传代。

 
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