血原性免疫 的英文怎麼說

中文拼音 [xiěyuánxìngmiǎn]
血原性免疫 英文
hematogenic immunity
  • : 血名詞(血液 多用於口語) blood:吐血 spit (up) blood; 血的教訓 a lesson paid for [written] in b...
  • : Ⅰ形容詞1 (最初的; 原來的) primary; original; former 2 (沒有加工的) unprocessed; raw Ⅱ動詞(原...
  • : Ⅰ名詞1 (性格) nature; character; disposition 2 (性能; 性質) property; quality 3 (性別) sex ...
  • : Ⅰ動詞1 (去掉;除掉) dismiss; relieve; remove 2 (避免) avoid; escape; avert 3 (免去) excuse s...
  • : 名詞(瘟疫) epidemic disease; pestilence
  1. A rabbit was infected with a cloned yntatl, blood was collecting from from the rabbit every 3 days after infection within 30 days, 10 clonal trypanosome populations were gotten, infecting a new rabbit by the last non - cloned trypanosome population. repeated above all, thus infected 5 rabbits sequentially. twenty different vats ( variant antigen type ) were monitored and characterized from those fifty mono - clonal populations by indirect immunofluorescence test ( ift ) and avidin biotin enzyme immunoassay ( abc - eia )

    用伊氏錐蟲雲南水牛單克隆株yntat1感染兔,感染后30天內,每3天從兔中分離錐蟲並單蟲克隆,最後一個未單蟲克隆的蟲株感染另一隻兔,重復以上操作,這樣順序感染5隻兔子,共獲得50個單克隆錐蟲種群( tp ) ,經間接熒光和abc酶標試驗鑒定共為20個抗互不相同的抗變異體( vats ) 。
  2. From dead chickens, one virrus was isolated by using eggs and chicken embryo fibroblast. lt was able to agglutinate chicken ' s erythrocytes and this heamagglutination could be inhibited by newcastle disease antiserum. this strain ' s biological property was tested by barren spot, cross - enutralization and cross - heamagglution inhibited and it was found that it was homological with the standard newcastle disease virus ( ndv ) virulent strain and avirulent strain but it had some diference with the standard strain

    本實驗採用spf雞胚及雞胚代成纖維細胞,從河北省某雞場新城抗體很高的病死雞的腦組織中分離得到一株病毒。此株病毒能凝集雞的紅細胞,並且這種凝集可以被特異清所抑制。
  3. Determination of imunogenicity of bivalent inactivated hrrs vaccine

    雙價腎綜合征出熱滅活檢測
  4. Negatie results of tests for ceruloplasmin, antinuclear antibodies, and antimitochondrial antibodies do not definitiely rule out wilson ' s disease, autoimmune hepatitis, or primary biliary cirrhosis, respectiely ; howeer, these diseases do not adequately explain the other features of this patient ' s presentation

    漿銅藍蛋白、抗核抗體和抗線粒體抗體檢查結果陰並不能排除肝豆狀核變、自身肝炎或膽汁肝硬變,然而,這些疾病各自並不能充分地解釋該患者的其他臨床表現。
  5. Section two the evaluation of biocompatibility of the acellular dermal matrix by the method of cell culture. the new born rat ' s epdermic cells were cultured with the acellular dermal matrix together as experiment group, while the epdermic cell were cultured simply as control. 24 hours later, under the invert microscope, the epidermic cells anchored well and transparent flat cells were observed in both groups. 7 days later, both cultured cells were taked out and fixed in 95 % ethanol, stained with hematoxylin and were observed under light microscope. many cleaved cells were observed in both groups. during cell culture, no pathogenic microganism was observed. so we considered the acellular dermal matrix was aseptic and had good biocompatibility. section three subdermal implantation of the acellular dermal matrix. 24 rats were used in the experiments. a piece of acellular dermal matrix ( 1. 5 x 1. 5cm2 ) was implanted beneath the dorsum skin flaps of each rat, 1 week, 2 weeks, 3 weeks and 4 weeks after implantation, 6 pieces of acellular dermal matrix were harvested and the size of implanted acellular dermal matrix were measured, the sections were used for he staining and observed under light microscope. the result were as folio wing : 1 - 2 weeks after implantation, the acellular dermal matrix began to adhere to the tissue around and turned red gradually ; 3 - 4weeks after implantation, the acellular dermal matrix adhered closely to the tissue around and could be recognized easily, 1 - 3 weeks after implantation, the size of implanted acellular dermal matrix had no statistical difference ( p > 0. 05 ). 4 weeks after implantation implanted acellular dermal matrix contracted ( p < 0. 05 ). under light microscope, l - 2weeks after implantation, the fibroblast cells infiltrated the acellular dermal matrix and a small amount endothelial cells of vessel and lympho - histiocytic cells infiltrated the acellular dermal matrix. 3 - 4 weeks after implantation, infiltrating blood vessels were evident. so we think that the acellular dermal matrix had low immunological reactions and could induce the infiltration of fibroblast macrophage cell and the endothelial cells of vessel

    結果如下:皮下包埋卜周者,無細胞真皮基質漸與周圍組織粘附,顏色由蒼白轉紅;皮下包埋3周者,無細胞真皮基質與周圍組織緊密枯附,盾晰葉辯;術后卜周,包埋的基質面積變化較包埋前無統計學差異o川0引,術后4周包埋的無細胞真皮基質面積較包埋前縮小j刃刀5 ) 。光鏡下術后卜周,宿主的淋巳組織細胞、成纖維細胞浸入生長,釉附在膠纖維上,少量管內皮細胞浸入基質;術后34周,無細胞真皮基質內較多的管形成,故可認為無細胞真皮基質低,能誘導宿主的成纖維細胞、巨噬細胞浸入生長,為一種新型的真皮替代物。第四部分無細胞真皮基質與自體斷層皮片復合移棺的研究, sd大鼠10隻,在其背部卜方造成全厚皮膚缺損的創面
  6. Experiment shows that the antigen extracted by autoclave is best for dot - ppa - elisa. applying the x2 test, optimal concentration of antigen was determined, and the optimum dilution of enzyme hrp - spa was 1 : 10. the high specificity of dot - ppa - elisa was proved by the specific blocking test, and also by the cross - reaction test in which the diaphragm does not react with the antibodies against salmonellosis, pasteurellosis, chlamydiosis, hcv, ppv, brucellosis, erysipelas suis, colibacillosis, prv

    試驗中對多種方法提取的診斷抗進行了比較、篩選;確定了dot - ppa - elisa的最佳工作條件;測定了st - 171株的清抗體及c群、 2型人工感染豬清抗體效價,並初步確定了該方法的陽標準。
  7. In group a, rabbits were immunized with isologous lens antigens ( il - ags ), + cfa while in group b rabbits were injected with pbs + cfa

    方法:採用同種晶狀體抗家兔;觀察清特異抗體水平,晶狀體病理和裂隙燈下晶狀體形態學變化以及視覺電生理改變。
  8. Guan xiaohong, et al. ( 1991 ) established a strain of monoclonal anti - idiotypic antibody np30 of schistosoma japonicum, whice is an internal image antigen of gut associated antigen ( gaa ), its antibody isotype is igm. np30 has a partial cross - reaction with soluble egg antigen ( sba ) and membrane associated antigen ( maa )

    管曉虹等建立的日本吸蟲單克隆抗獨特型抗體( anti - id , ab _ 2 ) np30是腸相關抗( gaa )的內影像anti - id ,與可溶蟲卵抗( sea )有交叉反應,可替代蟲源用於吸蟲病診斷和抗病苗的研究。
  9. By recognizing and binding to certain carbohydrate moieties on various pathogens, it can promote the killing of microbes either by acting directly as an opsonin or by activating the lectin complement pathway. however, the function of mbl depends on a certain of levels of serum mbl. mbl deficiency and low levels of serum mbl are the basis for a common opsonic deficiency and are associated with recurrent infections and autoimmune diseases such as systemic lupus erythematosus and rheumatoid arthritis

    然而, mbl功能的發揮有賴于其一定的清濃度, mbl缺乏或清濃度過低是引起調理吞噬缺損的根本因,可增加機體對各種病微生物的易感而導致機體反復感染,並且與自身疾病如系統紅斑狼瘡( systemiclupuserythematosus , sle ) 、類風濕關節炎( rheumatoidarthritis , ra )的發生、發展有關。
  10. This modification includes : ( 1 ) selecting two important molecules as candidates, ( 2 ) choosing a promiscuous t - cell epitope, and two b - cell epitopes or conserved amino acid sequences from the two important molecules, ( 3 ) connecting them adequately through analysis by the molecule designing software. therefore, the synthetic new antigen may interfere with the process of fertilization by multiple ways and its contraceptive effects may be enhancing. based on the molecule designing methods, the b - lymphocyte cell epitope of sperm / testis specific protein sp17 and cyritestin which interfere with fertilization in mouse, as well as the promiscuous th cell epitope of the ribonuclease ( rnase ) in bovine were selected

    本研究以蛋白質分子設計的理論和方法研究避孕苗,將sp17和cyritestin關鍵表位和牛核糖核酸酶非選擇th細胞表位合理組合,獲得新抗- 35肽序列;並在合成、純化後分別與弗氏佐劑、刺激復合物( iscoms )混合后不同遺傳背景的雌小鼠,觀察清和生殖道內的特異抗體滴度的動態變化、生育力的改變以及后小鼠重要臟器的組織病理學改變:以及在ivf下,新抗的特異清對精卵相互作用的影響及抗在精子表面的特異定位。
  11. After the recombinant plasmid pcdna3. 1 / ts87 was identified by digestion of hindlll and bamh i, it transformed into cos7 by lipofectamine. expression product was identified by immunohistochemical method, sds - page and western - blot. the immunocytochemistry result has shown that specific brown - staining grains were found in the cytoplasm of cells transformed by recombinant plasmid versus not seen in cells transformed by pcdna3. 1 or normal cells ; the sds - page result has revealed that a band about 3 8kb was found in cell lysis transformed by recombinant plasmid versus not in cells transformed by pcdnas. l or normal cells ; the western - blot result has showed that only the band about 38kd was recognized by sera from rabbit infected by t. s artificially and sera from rabbit immunized with soluble antigen of t. s and with protein expressed by ts87 gene and by a monoclonal antibody of t. s

    通過細胞的組化,細胞裂解物的sds - page電泳, westem - blot分析檢測目的基因的表達情況。組化結果顯示:重組質粒轉染的細胞質中有棕褐色顆粒,而空載體轉染細胞及正常細胞無此現象;細胞裂解物sds - page電泳結果顯示:只有重組質粒轉染的細胞在約38kd處有明顯的蛋白帶,這與理論計算的ts87基因表達蛋白的分子量為38kd基本一致; western - blot分析結果顯示:約38kd的蛋白帶能夠分別被旋毛蟲感染兔清,成蟲蟲體可溶清, ts87基因核表達蛋白清( ts87清)以及一株具保護的旋毛蟲單抗特異識別。
  12. The endocrine cells in the digestive and glands of alligator sinensis embryos aged from 8th to 55th day were localized and compared by using immunohistochemical method with thirteen kinds of antiseras of hormone. during the development of pancreas in alligator sinensis embryos, somatostatin ( ss ) immunoreactive ( ir ) cells, 5 - hydroxytryptamine ( 5 - ht ) - ir cells, glucagon ( glu ) - ir cells, epidermal growth factor ( egf ) - ir cells appeared on 18th day. no p53 protein - ir cell, gastrin - ir cell, testosterone - ir cell, chromogranin a - ir cell, vasoactive intestinal polypeptide - ir cell, epithelial membrane antigen - ir cell or insulin - ir cell was found in the pancreas of alligator sinensis embryos

    本實驗採用組織化學技術,應用13種不同的抗清,對孵育時間8 ? 55天揚子鱷胚胎消化道及消化腺內分泌細胞的種類進行鑒別、定位和比較,結果如下:揚子鱷胚胎胰腺中,生長抑素、 5 ?羥色胺、胰高糖素、表皮生長因子、胰多肽反應陽細胞出現于第8天; p物質細胞出現于第18天; p53 、胃泌素、睪酮、嗜鉻素a 、管活腸肽、上皮膜骯、胰島素細胞在各期揚子鱷胚胎胰腺中均未發現。
  13. 6. hc and ha antigens were separated by sds - page from nature hypoderma sp larve, then immunized rabbitsrespectivelly, hc and ha positive serum were preparated. 7

    從天然皮蠅幼蟲中提取了皮蠅抗,通過sds一page分離獲得了hypoderminc和hypodermina天然抗,用此抗家兔,制備了皮蠅hypoderminc和hypodermina陽清。
  14. The characteristics of this method are : a, directly counting cell number without the influence of the metabolic state of the cells ; b, discrimination of target cells from effector cells in cell - mediated cytotoxicity assay ; c, less treatment step, and free - radioactivity ; d, high sensitivity and reliability. 2, using the above assay, immunofluorescent labeled technique, and flow cytometry, the pbmc proliferation, apoptosis, necrosis, cell cycle, activation, cytokines and membrane marker were detected. the results showed that the number of pbmc reduced, but the activity of pbmc increased dose - dependently ; the reduction of cell number resulted from necrosis and apoptosis ; the supernatant of k562 cell lines were not able to block the cell cycle, but to promote it ; the ratio of t cell subset and the expression of thl and th2 cytokines increased

    結合以上創建的方法和熒光流式細胞術,用k562細胞株可溶分泌物(上清)對外周單個核細胞( pbmc )進行培養以模擬體內微環境,然後分別從細胞增殖、凋亡、壞死、細胞周期、活、細胞因子和表面抗表達等方面進行研究,結果發現用腫瘤上清培養的pbmc細胞數量下降明顯,但同時對其有激活作用,且呈劑量依賴;細胞數的下降主要是由細胞壞死和凋亡引起的,腫瘤上清對細胞周期沒有阻斷作用,反而略有促進作用; t細胞亞群比例增加,並促進表達th1 、 th2細胞因子。
  15. 3 immunogenicity of m3m4 loop recombinant peptide antigen of nr1, neuroexcitotoxicity protective effects and their mechanisms study of antiserum against m3m4 ( 1 ) to explore the immunogenicity of m3m4 loop recombinant peptide vaccine, m3m4 recombinant peptide was injected subcutaneously to immunize balb / c mice ( h - 2 ), cd4 / cd8 t lymphocytes subsets, the cytokine levels in serum and the liter of specific humoral response were detected with facs, indirect elisa and elisa separately

    ,抗清還可以結合合成膚nps ,證明該表位具有和抗。收集抗清用於功能檢測。 (二) m3m4片段抗清抗興奮毒損害作用以臺盼藍染色法和位末端標記( tun 』 el )法觀察抗清對代培養海馬神經元興奮毒壞死和凋亡的保護效應。
  16. The results from sds - page presented that there were three female specific protein subunits with molecular weights of 123 kd, 120 kd and 91 kd, respectively. we can conclude the higher molecular compose of two subunits ; the results from two dimension electrophoresis showed the isoelectric points of two female - specific spots with molecular weight of about 120kd were 5. 5 and 5. 7. immunodiffusion reactions demonstrated that vg existed both in female fat body and hemolymph, which as vn was deposited in the ovary, while not in the male

    Page電泳結果表明:麗蠅蛹集金小蜂明顯存在2條雌特異帶-卵黃蛋白,分子量分別為181kd和136kd ; sds - page電泳分析:存在3條雌特異帶,其分子量為123kd 、 120kd和91kd ,由此,可推定卵黃蛋白( vitellogenin , vg )和卵黃磷蛋白( vitellin , vn )由2個蛋白組成,其中分子量較大的蛋白由2個亞基組成;雙向電泳結果顯示,在120kd附近有兩個特異點,其等電點為5 . 5和5 . 7 ;雙擴散表明,麗蠅蛹集金小蜂卵黃磷蛋白的抗清與雌隱成蟲蟲體、脂肪體、淋巴和卵巢勻漿液均有沉澱反應,而與雄蜂淋巴無反應,說明了vg與vn具有同源,是雌特異蛋白,且由脂肪體合成。
  17. These essential component, hemagglutination, toxicity, immunogenicity of mycoplasma hyopneumoniae strain xy - 1 membrane protein were studied. the range of membrane protein mw is from 14kd to 100kd by means of sodium dodecyl sulfate - polyacrylamide gel electrophoresis, and molecular weights of the protective antigens were 36kd and 64kd by sds - page

    本研究以分離豬肺炎支體野毒株( xy - 1株)的膜蛋白為試驗材料,系統地研究了膜蛋白的分子量范圍、、毒等。
  18. The expression of recombinant infectious bursal disease ( ibdv ) vp2 gene in transgenic tobacco was studied. it revealed that the vp2 produced in transgenic tobacco could react with serum specific for ibdv. these results were the basic of investigating the immunological function of foreign protein vp2 produced in transgenic plants and bolstered the concept of using transgenic plants for a novel, edible, safe vaccine production

    研究了傳染法氏囊病病毒抗蛋白基因ibdvvp2在煙草中的表達情況,證明轉基因煙草中產生了能與ibdv特異抗清反應的ibdv抗蛋白,為研究轉基因植物中生產的外源蛋白vp2的學功能奠定了基礎,並為利用轉基因植物生產可食苗提供了實驗依據。
  19. The high titer specific ndrg2 antibody is indispensable to reseach deeply the functions or the tissue and subcellular distribution features of ndrg2, ha order to prepare ndrg2 antibody, the whole ndrgl sequence was cloned into prset - a vector and two truncated sequences of ndrg2 were cloned into pgex - 4t - l vector. after induced by iptg, the fusion proteins were expressed in e. coli ; rabbits immunized with the whole length ndrg2 protein were reinforced with two shortened fragments of ndrg2 ; after immunization, rabbits produced high titer antiserum against ndrg2. then antisemm was absorbed using ndrg2 antigen immobilized on nc filters, the purified product of antiserum shows high special to ndrg2 protein, and the separated inclusion body of 6his - ndrg2 will be useful for the further reseach

    為制備高效價的ndrgz抗體,分別構建了prset a雌、 pgex4t d唾倉和pgex4tl七三種核重組表達質粒,並在大腸桿菌中誘導表達出相應的融合蛋白;用全長gstjqdrgz蛋白兔,然後用gst ndrgz人和gstjqdrgze片段加強,經得到了較高效價的兔抗人ndrz多克隆抗清,利用固定於硝酸纖維素膜上的ndrgz抗親和吸附純化抗清,提高了ndrgz抗體的特異;並對包涵體形式表達的6his ndrgz進行初步的分離純化。
  20. Immune mediated thrombocytopenia ( itp ) is a common manifestation of autoimmune disease in children

    小板減少紫癜( itp )是一種常見的兒童自發病。
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