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  现场
    Using parasitic site isolating and single oocyst infected techniques, we have gained pure spe- cies of Eimeria necatrix from mixed species of chicken coccidia in field.
    采用从寄生部位分离和单卵囊感染技术,对现场采集的鸡球虫混合种进行单种纯化,获得了毒害艾美球虫(Eimeria necatrix)。
短句来源
    The results indicated that LAT has advantages such as simple、rapid、sensitive、specific and detectable on site and so on,it is a new method that is suitable for grass-roots unit to detect serum antibodies against chicken NDV.
    结果表明 ,乳胶凝集试验具有操作简便、快速、敏感性高、特异性强且可用于现场检测等优点 ,是一种适合基层单位用来检测鸡新城疫病毒血清抗体的新方法
短句来源
    Positive numbers are 16 in manuforage by LAT. Positive samples are 18 in manuforage,The coincidence rate of both methods reached 83.8% in manuforage. The results showed that LAT has advantages such as simply,rapidly,sensitively,specifically and detects on site and to on.
    用所建立的乳胶凝集试验方法和常规分离培养检测法检测75份成品饲料,结果乳胶凝集试验成品饲料阳性16份,常规分离培养检测法成品饲料阳性18份,两种方法的阳性符合率成品饲料为83.3%,结果表明乳胶凝集试验具有操作简便、省时、特异性强且可用于现场检测等优点,是一种适合基层单位用来检测沙门氏菌的可靠方法。
短句来源
    The results indicated that LAT has advantages such as simple,rapid,sensitive,specific and detectable on site and so on,it is suitable for grass-root unit to detect serum antibodies against IBDV.
    试验表明乳胶凝集试验操作简便、快速、敏感性高、特异性强,可用于现场检测,适合基层单位检测IBDV血清抗体。
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  位点
    The Study on the Target Site of Porcine Myostatin
    猪肌生成抑制素作用靶位点的研究
短句来源
    The Isolation, Cloning and Expression of the Fusion Protein Cleavage Site Gene of the Newcastle Disease Virus in the Protoryotic Cells
    新城疫病毒融合蛋白裂解位点基因的分离克隆及在原核细胞中的表达
短句来源
    Molecular Cloning and Sequencing of the Cleavage Site of F0 Protein from the Isolate of Pigeon Newcastle Disease
    鸽新城疫病毒分离株F0裂解位点的基因克隆及序列分析
短句来源
    The polymorphic fragments amplified by both primers were cloned and sequenced. The sequencing results showed that there was transition(T-C) at 645 site and(G-A)at 641 site,one transition(T-C)at 3 264 site of EX-FABP gene in chicken, respectively.
    引物1和引物2的多态性片段测序分析表明,EX-FABP基因第641位点和645位点分别发生了单碱基的转换(G-A和T-C),第3264位点发生了转换(T-C)。
短句来源
    The fragment of Actinobacillus pleuropneumonia APXⅡ gene was cloned into the multiple cloning site of Eukytote expressing vector pET-28a,The recombinant of pET-APXⅡ was cultivated and induced with IPTG.
    将猪传染性胸膜肺炎放线杆菌APXⅡ的一段毒素基因克隆到原核表达载体pET-28a(+)的多克隆位点中,经鉴定后得到重组质粒pET-APXⅡ,并将其转化到受体菌BL21中,诱导剂IPTG进行诱导表达,4 h后达到高峰。
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    We synthesized gene fragment of the active site of the coagulation factor X by RT-PCR from the liver of the mice. We construct the expression vector pET28-HSP65-FXa by connect gene fragment with the HSP65gene fragment. The HSP65-FXa fusing protein is expressed in the E .
    我们采用RT-PCR方法从小鼠肝组织中钓取了编码凝血因子X活性部位(FXa)的基因片段,并将其与HSP65基因相融合,构建了pET28-HSP65-FXa表达载体,在大肠杆菌中表达出HSP65-FXa融合蛋白。
短句来源
    In the group pCISI and pEGISI , three different dosages( 10, 50 and 100 μg/100 μ L) for each animal were respectively injected at the same site as the pretreatment.
    6个实验组:2种真核表达质粒(pCISI和pEGISI)分别按10μg/100μL、50μg/100μL、100μg/100μL共3个剂量于预处理相同部位注射;
短句来源
    T1-T3, namely the groups of plasmid pES/2SS(T1), pES/2SS-CpG (T2) and pES/2SS+pE-CpG(T3) at 20μg/20μl dosage, were injected at the same site as the pretreatment.
    三个实验组(T1~T3):真核表达质粒pES/SS(T1)、pES/2SS-CpG(T2)、pES/2SS+pE-CpG(T3)按剂量20μg/20μl于预处理相同部位注射;
短句来源
    1. Tracing antibacterial active site of V. yedoensis.
    1.紫花地丁抗菌活性部位追踪。
短句来源
    A in situ hybridization(ISH) method was used to detect low copy FMDV in infected cells,in order to illuminate FMDV multiplication site. In this study,FMDV RNA was located and detected in BHK-21 cells by ISH. Cells infected experimentally with O/Akesu/58(10~7TCID_(50)) at 2,4,6,8 and 10 hours post-inoculation.
    为了明确FMDV在细胞内的增殖部位,建立检测细胞内低拷贝FMDV的方法,对试验接种FMDV O/Akesu/58(107TCID50)毒株的BHK-21细胞中2~10 h不同时间段的病毒RNA进行检测和定位。
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  场地
    The results showed: the effects of site, species(strain), day-age and sex were extremely significant on the content of TP(P<0.01);
    结果表明:场地、品种(系)、日龄及性别对TP含量的影响极显著(P<0.01);
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Therefore, van der Waals' interactions between acetylcholinesterase and these drugs are stronger than those between butyrylcholinesterase probably due to a small active site gorge and a significant peripheral anionic site for acetylcholinesterase.
      
Novel 5-substituted esters and homologous ester and amido derivatives of 4,5 dihydro-3,3-diethyl-2(3H)-furanone were synthesized and evaluated for anticonvulsant activity in rodents and for affinity to a site on the GABAA receptor complex ([3H]TBOB).
      
The results showed that these compounds are capable of important interactions with the NNRT binding site, which encouraged us to submit them for biological assay.
      
From these data, it may be deduced that the administration of high concentration of 18-methyl norethindrone can displace ketoprofen from its secondary binding site.
      
This work attempts to calculate the binding-site number using fluorescence spectroscopic method with bovine serum albumin (BSA) and Indo-1 as protein and ligand models, respectively.
      
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