outer membrane protein造句
例句與造句
- The cloning of 26kda outer membrane protein gene of helicobacter pylori
外膜蛋白的基因克隆 - Gene cloning and expression of outer membrane protein of helicobacter pylori
幽門螺桿菌外膜蛋白的基因克隆及表達(dá) - Cloning and expression of gene encoding helicobacter pylori outer membrane protein with mr
000外膜蛋白編碼基因的克隆及表達(dá) - Outer membrane protein , omp
外膜蛋白 - On relation between helicobacter pylori outer membrane protein and digest system disease
幽門螺桿菌外膜蛋白與消化系疾病關(guān)系的研究 - It's difficult to find outer membrane protein in a sentence. 用outer membrane protein造句挺難的
- The kind of the y . pestis out membrane protein and the application of gene type in china
中國(guó)鼠疫菌外膜蛋白種類及在基因分型中的應(yīng)用 - The cloning and recombinant vector constructing of lower - weight outer membrane protein encoding gene of helicobacter pylori
幽門螺桿菌低分子質(zhì)量外膜蛋白編碼基因的克隆與重組載體構(gòu)建 - Preparation , purification and identification of polyclonal antibodies of vibrio alginolyticus and outer membrane proteins of vibrio alginolyticus
溶藻弧菌菌體及其外膜蛋白多克隆抗體的研究 - Construction of the eukaryotic expression vector for the gene encoding the 26 kda outer membrane protein of helicobacter pylori and identification of the expressed proteins
000外膜蛋白真核載體的構(gòu)建及表達(dá)蛋白的鑒定 - A dot - ppa - elisa method has been developed to detect the antibody in swine serum against pasteurellosis . the capsule polysaccharide and outer membrane protein of pasteurella multocida was prepared as the diaphragm antigen
本研究提取豬巴氏桿菌菌株的莢膜和外膜蛋白抗原，首次建立了檢測(cè)豬巴氏桿菌病血清抗體的dot - ppa - elisa方法。 - Haake da , champion ci , martinich c , et al . molecular cloning and sequence analysis of the gene encoding ompl1 , a transmembrane outer membrane protein of pathogenic leptospira spp [ j ] . j bacteriol , 1993 , 175 ( 13 ) : 4225
晏菊芳,鮑朗,伍衛(wèi)華,等.中國(guó)鉤端螺旋體強(qiáng)毒株017膜蛋白基因的質(zhì)粒載體構(gòu)建及表達(dá)[ j ] .中華微生物學(xué)和免疫學(xué)雜志, 1999 , 99 ( 2 ) : 117 - With bacterial cgc as main subject , the tests had been done to elucidate mechanism of self - organization for macroscopic rhythmic structure . the dynamics of cgc forming was observed by special techniques of waving culture and microscopic culture ; the differences in outer structure of cell wall and flagella number had been observed by atomic force microscope scanning ; integrity of cell wall was examined under tem ; outer membrane protein was analysed by sds - page and various substance and factors for cgc formation were determined
采用特殊的波動(dòng)培養(yǎng)和顯微培養(yǎng)技術(shù)觀察潛生體形成動(dòng)態(tài)；應(yīng)用原子力顯微鏡掃描，比較細(xì)菌潛生體與繁殖體在細(xì)胞壁外層結(jié)構(gòu)和鞭毛數(shù)量的差別；用透射電鏡觀察細(xì)胞壁完整性，以十二烷基硫酸鈉?聚丙烯酰胺凝膠電泳分析外膜蛋白的改變，并通過實(shí)驗(yàn)分析多種物質(zhì)和因素對(duì)潛生體形成的影響。 - The major outer membrane proteins ( momps ) of an aeromonas hydrophila named ahl316 which isolated from diseased eel and the referential strain ahtps - 30 were purified and used for preparing immunostimulating complexs ( momp - iscoms ) . the immunotrial was carried out by injecting european eel peritoneally with 20ug of momp - iscoms per eel
本研究選取鰻源嗜水氣單胞菌l316和參考菌株嗜水氣單胞菌tps - 30 ，分別制備了這兩株菌主要外膜蛋白免疫刺激復(fù)合物( momp - iscoms ) 。 - The results demonstrated that the momps were protective antigens and the momp - iscoms of aeromonas hydrophila could induce the host to mount satisfied immunity . a pair of primers were designed according to the published nucleotide sequence of a putative outer membrane protein gene ( omp ) of aeromonas hydrophila . with the specific primers , a target fragment about 1 . 1kb was amplified from aeromonas hydrophila l316 via pcr . the target fragment was inserted into the linearized pgem - t easy vector
根據(jù)已發(fā)表嗜水氣單胞菌的外膜蛋白基因omp的核苷酸序列設(shè)計(jì)引物，利用pcr技術(shù)，擴(kuò)增、克隆了嗜水氣單胞菌l316的主要外膜蛋白基因( momp ) ，經(jīng)t a克隆，插入到pgem - t系列載體上，測(cè)序分析結(jié)果表明momp基因最長(zhǎng)的開放閱讀框( orf )為1035nt ，編碼由344個(gè)氨基酸組成，分子量為36kda的主要外膜蛋白質(zhì)( momp ) 。 - Make all these together , it proved that the cloned gene represented the major outer membrane protein gene of ahl316 , and the expressed gene products shared identical antigenicity with the natural main outer membrane protein . the studies on preparation and application of momp - iscoms of ah l316 provided a new approach to fish vaccinology . the successfully cloning and expressing the major outer membrane protein gene of ah l316 made it possible to describe this gene ' s function under a single factor level , and also provided technical support for developing an advanced gene engineering vaccine and subunit vaccine against aeromonas hydrophila
鰻源嗜水氣單胞菌l316主要外膜蛋白免疫刺激復(fù)合物的制備與應(yīng)用研究，對(duì)研制魚類疫苗學(xué)問題進(jìn)行了新的初步探索；成功地克隆和表達(dá)嗜水氣單胞菌l316主要外膜蛋白基因?yàn)樵趩我蜃铀缴涎芯渴人畾鈫伟饽さ鞍椎淖饔煤兔庖吖δ芤约爸苽涫人畾鈫伟蚬こ桃呙绾蛠唵挝灰呙绲於夹g(shù)基礎(chǔ)。
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