母體毒性 的英文怎麼說

中文拼音 [mǔtǐdúxìng]
母體毒性 英文
matermal toxicity
  • 母 : Ⅰ名詞1 （母親） mother 2 （泛指女性長輩） one s elderly female relatives 3 （配套的兩件東西里的凹...
  • 體 : 體構詞成分。
  • 毒 : Ⅰ名詞1 （對生物體有害的性質或物質; 毒物） poison; toxin 2 （毒品） drug; narcotics 3 （姓氏） a s...
  • 性 : Ⅰ名詞1 （性格） nature; character; disposition 2 （性能; 性質） property; quality 3 （性別） sex ...
  • 母體 : 1 （孕育幼兒的人或雌性動物的身體） the mother s body; the （female） parent; parent body 2 [原子...
  • 毒性 : [藥理學] toxicity; virulence; poisonousness毒性測定 toxicity test
  1. Heamagglutination tests were applied to detect virus in allantoic fluid of chicken embryos which were infected by b95 gathered from the vaccinated chickens " cloacal and oral cavity. the results show that the virus may be detected from 2 days to 11 days after the chicken being vaccinated. the hi antibodies were measured by heamagglutination inhibition tests. there is no significant difference between the immunized and the control chickens which were fed in one case. chickens were immunized with b95 by different immunization meathods or with different vaccines by the same meathod. lt is demonstrated that eyedrop, drinking water, spray or muscle injection all can stimulate good effects, but eyedrop and spray seem to be the best meathods. b95 immunized chicken have relatively higher hi titers and it also can last for a longer time than others

    但如果兩者相隔10天以上免疫， b95免疫不受h120的影響；如果同時免疫b95和h120 ，加大b95的免疫劑量也能獲得良好的免疫效果。用棉拭子采b95免疫雞口腔、泄殖腔的分泌液，檢測其中病毒的存在，結果免疫后2 11天雞口腔和泄殖腔中均有病毒的存在，說明b95免疫雞帶毒時間長。研究結果表明， b95具有不受母源抗體干擾、 hi抗體產生快、水平高、持續時間長、同居擴散性強等特點，因此b95是一株優良的、具開發前景的新的新城疫疫苗株。
  2. Even so, by truncating hbv pres gene, we finally obtained some useful " " bailors ", either nontoxic or self - activating, and used them to fish dna fragments of hbv pres interacting protein ( s ) from an ad vector constructed human embryonic cdna library

    我們通過第回軍巨大學碩士學位論文對pres基因分段截短的方法，獲得了對酵母細胞即無毒性作用，又沒有自激活作用的「誘餌」 ，通過它在酵母雙雜交系統中篩選構建於ad載體的人胎肝。
  3. An establishment gram institute contains " the k factor " to be able to produce the strong effect immune body, suppression virus activeness, causes viral dna to be unable to duplicate, routs the cause of disease parent substance at one fell swoop, causes the virus to burst the death, never recurs

    安立克kj劑"系列藥物排出的病毒主要聚集在這個部位。安立克所含的「 k因子」能產生強效的抗體，抑制病毒活性，使病毒dna無法復制，一舉擊潰病原母體，使病毒破裂死亡，永不復發！
  4. Differential diagnosis included cerebral toxoplasmosis, cytomegalovirus ( cmv ) encephalitis, primary cns lymphoma, progressive multifocal leukoencephalopathy, fungal abcess due to candida, aspergillus, or cryptococcus, varicella - zoster virus encephalitis or vasculitis, herpes simplex encephalitis, tuberculosis ( m. tuberculosis ), and kaposi ' s sarcoma

    其它的診斷包括：腦弓形體病，巨細胞病毒（ cmv ）型腦炎，原發中樞系統淋巴瘤，漸進性多灶性腦白質病，假絲酵母菌，麴菌或隱球菌所致真菌性膿腫，水痘帶狀病毒型腦炎或脈管炎，單純皰疹腦炎，肺結核（多發性結核） ，和卡波西肉瘤。
  5. The hwtx - i gene was chemically synthesized according to its known cdna sequence, the gene was inserted into vector ppic9k which contained aoxj promotor and the sequence of a secreting signal peptide - a - factor, the cloning ppic9k / hwtx - i was constructed and confirmed by two - step pcr and dna sequence analysis, then it was transformed into host strain gs115, a his + muts cell line was screened and multicopy transformants were screened by various g418 concentrations, the multicopy transformant was named gh1. gh1 was cultivated in flasks. after 6 days of induction by 0. 5 % methanol, the supernatant was checked by 16. 5 % tricine - sds page, which showed there was a band in the position of 3. 5 - 6. 1kd, then it was isolated and desalted by ultrofiltration followed by ion exchange of cm column, after reverse phase hplc of ci8 and vacuum drying, the purified rhwtx - 1 was obtained which was proved to be correct recombinant hwtx - i by tricine sds - page, maldi - tof mass spectrometry, amino acid composition analysis, the n - terminal amino acid sequence and its biological activity, the final field of the purified rhwtx - i was about 80mg / l, accounting for 23. 6 % of it total secretory proteins

    將帶有hwtx -基因的ppic9k經blgii線性化后，轉化酵母宿主菌gs115原生質體后經篩選陽性克隆並經表型鑒定為his ~ + mut ~ s酵母菌，進一步用遺傳毒素g418篩選多拷貝的轉化菌株，命名為gh1 ；將gh1甲醇酵母菌用0 . 5的甲醇誘導表達，發酵上清經90飽和度的（ nh _ 4 ） _ 2so _ 4沉澱， yw - 3 （ mwc03000 ）的超濾膜超濾，再經cm陽離子交換， c _ （ 18 ）反相hplc純化得到分子量為4kd左右的組分，其中4289 . 05的組分經質譜鑒定，氨基酸組成分析和序列測定為正確的表達產物，生物學活性表明其活性為天然毒素活性70 % ，表達量為80mg / l 。
  6. Tile clinical course of acquired syphilis can be divided into three stages : primary, secondary and tertiary and it can attack almost all tile organs of the body including eyes

    除了經性接觸傳染的後天性梅毒，梅毒螺旋體更可經向母親之胎盤感染胎兒，造成先天性梅毒。
  7. In our work, different hbv pres gene fragments were amplified by pcr, cloned into pgbkt ? vector in yeast two - hybrid system 3, and then transformed ah 109 yeast cells. the results showed that these pres expression products were nontoxic to yeast cells, but all self - activated the yeast two - hybrid system

    本研究將hbv前s區不同片斷進行擴增，克隆入酵母雙雜交系統3中的pgbkt7載體，轉化酵母細胞ah109 ，經檢測，證實了hbv前s區不同片斷對酵母細胞無毒性作用，但是都存在自激活作用。
  8. In this study, pichia pastoris system had been utilized for expression of fmdv 2c3abc gene which aimed for establishing a sensitive and specific molecular dignosis method. first, 2c and 3abc genes were amplified individually from p2 and 3abc postive clones and ligated together using pcr method, then this 2c3abc product was cloned into pgem - t easy vector and transformed e. coli dh5a competent cell. a postive recombinant plasmid which contained whole 2c3abc gene had been confirmed by pcr, enzyme digestion and sequencing. after that, the 2c3abc gene was sub - cloned into ppiczaa expression vector and transformed e. coli dh5 a competent cell and selected by zeocin ? antibiotic. the postive recombinant expression vector was linerized and electro - transformed pichia pastoris smd1168 competent cell. a recombinant pichia pastoris had been obtained by zeocin ? antibiotics selection and induced with 0. 5 % methanol for target protein expression. the expression product was analysised by sds - page and western blotting assay. the result sh owed that 2c3abc gene was expressed successfully in pichia pastoris and the product was a 95ku fusion protein which could be recognized by anti - fmdv serum. the amount of target protein was over 15 % of the total bacteria protein by gel thin layer scanning analysis. this research had supplied materials for establishing a fmd diagnosis method to differentiate infected animals from vaccinated animals

    首先，用p2和3abc陽性克隆通過連接pcr方法獲得目的基因並將其克隆到pgem - teasy載體上，並轉化e colidh5a感受態細胞中，經pcr 、酶切以及測序證明得到了完整的2c3abc基因，並與國內外參考序列進行比較分析。然後，將目的基因亞克隆于ppiczaa表達載體並轉化大腸桿菌dh5a ，以zeocin ~ （ tm ）抗性篩選陽性克隆，大量提取重組表達質粒並用pme酶線性化后電轉化入畢赤酵母smd1168感受態細胞，通過zeocin ~ （ tm ）抗生素梯度濃度篩選，獲得重組酵母用0 . 5甲醇誘導表達，通過sds - page電泳、 westernblotting分析，結果表明， 2c3abc基因在畢赤酵母中成功表達，其表達產物為一95ku的融合蛋白，並能被口蹄疫病毒陽性血清識別。
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