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brucella相关的网络例句

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Campylobacter jejuni selected media supplied with egg and calf serum and Brucella broth supplemented with calf serum were used to cultivate Hp for reverting coccoid to bacterial under different conditions.

本研究通过对18株Hp在不同条件下的培养,观察其生存及形态变化,并在加有鸡蛋和小牛血清的空弯培养基上及加有血清有布氏肉汤培养基中是进行培养和返祖,观察其变异规律。

A double antigens Sandwich Enzymelinked Immunosor-bent Assay( DAgS -ELISA)have been developed under the basis o f higher titer and freeze dried production conjugate of Brucella antigen with horseradish peroxidase. Serumsamples formdiagnosed patients of Brucellosis and sheep,cattl e,swine infected with Bru-cella as well as normal men and those a nimals in laboratory detected throu gh DAgS -ELISA,SAT and RBPT tests.

方法在制备高滴度布氏菌抗原辣根过氧化物酶结合物及其冻干制品基础上,应用酶联免疫吸附双抗原夹心法即双抗原夹心酶联免疫吸附试验、试管凝集试验及虎红平板凝集试验对从山西省布氏菌病疫区收集的布氏菌病患者、布氏菌感染羊、牛、猪以及健康人、羊、牛、猪共计290份血清进行对比检测。

Methods : OMP2b protein gene fragment was amplified from genomic DNA of Brucella ovis in XinJiang through PCR.

采用PCR扩增技术,从新疆绵羊种布鲁氏菌基因组DNA中扩增出OMP2b基因片段,将该片段克隆于原核表达载体PE-28a,构建成重组质粒,IPTG诱导表达,SDS-PAGE检测有无蛋白的表达。

Out membrane protein of Brucella ovis ; OMP2b gene fragment ; clone ; expression

绵羊种布鲁氏菌外膜蛋白OMP36; OMP2b基因;克隆;表达

Objective: to express OMP2b antigen protein of OMP36 from out membrane protein of Brucella ovis in XinJiang and study the probability for it as molecular bacterin and diagnose antigen.

以表达新疆绵羊种布鲁氏菌外膜抗原蛋白OMP36的表达蛋白OMP2b,探索其作为诊断抗原和分子疫苗的可能性。

The specific PCR products of approximately 112bp in length was amplified from the other 10 strains of E.faecalis from lamb naturally infected with E.faecalis,lamb and mouse experimentally infected with E.faecalis by the PCR assay,but no any bands were amplified from Streptococcus equi subsp.equi,Streptococcus G,Streptococcus A,Staphylococcus aureus,Listeria monocytogenes from sheep,Mycoplasma ovipneumoniae and Brucella ovis.

应用该方法对分离的致羔羊脑炎粪肠球菌、由肠球菌导致发病或死亡羔羊脏器以及人工感染死亡小鼠的主要脏器进行扩增,均能得到特异性的DNA条带;对其他7种病原菌,马腺疫链球菌C群、G群链球菌、A群链球菌、金黄色葡萄球菌、羊源李氏杆菌、绵羊布氏杆菌、绵羊肺炎支原体不能扩增出特异的DNA条带。

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