血清中和反應 的英文怎麼說

中文拼音 [xiěqīngzhōngfǎnyīng]
血清中和反應 英文
serum neutralization
  • : 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 (純凈) unmixed; clear 2 (寂靜) quiet 3 (清楚) distinct; clarified 4 (一點不留) w...
  • : 和動詞(在粉狀物中加液體攪拌或揉弄使有黏性) mix (powder) with water, etc. : 和點兒灰泥 prepare some plaster
  • : Ⅰ名詞1 (方向相背) reverse side 2 (造反) rebellion 3 (指反革命、反動派) counterrevolutionari...
  • : 應動詞1 (回答) answer; respond to; echo 2 (滿足要求) comply with; grant 3 (順應; 適應) suit...
  • 血清 : [免疫學] serum; blood serum血清病 serum sickness
  1. The determination of human thymidine kinase ( htk ) in human serum, which is a key indicator of cancers can give information for the diagnosis and treatment of the malign diseases. the protein a layer was first self - assembled onto the gold electrode surfaces of quartz crystals, the monoclonal antibodies were then orientedly immobilized through the specific binding between the fc terminals of the antibodies and the self - assembled protein a. with this sensor, the affinity constant of antigen - antibody binding was estimated to be 1. 85 106 l / mol according to the scatchard ’ s plotting method, which proved the high bioactivity of antibody. finally, an amplified piezoelectric immunosensor was designed to determine the htk in

    實驗將蛋白a吸附於鍍金壓電石英晶體電極表面,用於定向固定htk單克隆抗體,成功研製了檢測htk的壓電石英晶體傳感器,並基於標準scatchard繪圖法,計算出免疫的親常數為1 . 85 106l / mol ,證明該單克隆抗體具有較高的免疫活性;同時基於酶催化沉澱技術,設計了的檢測htk的質量放大壓電石英晶體傳感器,該傳感器可在0 . 1 - 10ng范圍內對htk進行定量檢測,用此傳感器成功地對5種癌癥病人htk的濃度進行了測定,實驗結果為癌癥的臨床診斷與治療提供了參考。
  2. 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

    本實驗採用免疫組織化學技術,用13種不同的抗,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、定位比較,結果如下:揚子鱷胚胎胰腺,生長抑素、 5 ?羥色胺、胰高糖素、表皮生長因子、胰多肽免疫陽性細胞出現于第8天; p物質免疫陽性細胞出現于第18天; p53 、胃泌素、睪酮、嗜鉻素a 、管活性腸肽、上皮膜骯原、胰島素免疫陽性細胞在各期揚子鱷胚胎胰腺均未發現。
  3. 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條雌特異性帶-卵黃蛋白,分子量分別為181kd136kd ; sds - page電泳分析:存在3條雌特異性帶,其分子量為123kd 、 120kd91kd ,由此,可推定卵黃原蛋白( vitellogenin , vg )卵黃磷蛋白( vitellin , vn )由2個蛋白組成,其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附近有兩個特異性點,其等電點為5 . 55 . 7 ;雙擴散表明,麗蠅蛹集金小蜂卵黃磷蛋白的抗與雌隱成蟲蟲體、脂肪體、淋巴卵巢勻漿液均有免疫沉澱,而與雄蜂淋巴無免疫,說明了vg與vn具有免疫同源性,是雌特異性蛋白,且由脂肪體合成。
  4. Hbv genotype was determined by the restriction fragment length polymorphism analysis in patients with chronic hbv infection in 5 cities of fujian province. 2. the sensitivities and specialties of melting curve assay and pcr microplate hybridization - elisa assay were compared with mpcr - rflp and sequence analysis for the detection of hbv ymdd mutants in 44 serums from patients receiving lamivudine monitherapy with viral breakthrough

    用熔解曲線法pcr微板核酸雜交- elisa法對44例接受拉米夫定治療過程出現病毒學跳時的進行ymdd突變株的檢測,並與測序法mpcr - rflp法比較它們的敏感性、一致性。
  5. No trace of any newly expressed protein band was noticed in supernant as well as in the cells by sds - page, except the verification of the substitution of beta - galactosidase gene ( the lose of galactosidase protein band ), which is a selective marker of the wild - type virus. elisa test results suggested the expression of egf in cells, but not in culture supernant. the quantitative calculation suggested the expressed egf was about 6 - 7 u g ( as egf standard ) per flask ( 2 > < 106 cells ) in the cellular extract

    將重組病毒rbmbacph - egf以10moi感染bmn細胞, 72小時后收集培養細胞;培養上經超聲波處理的細胞樣品elisa檢測發現胞內樣品存在能與egf抗體免疫的產物,粗略估計表達量約6 7 g 2 10 ~ 6個細胞(相當于egf標準品) ;重組病毒rbmbacph - egf穿刺接種5齡家蠶幼蟲,每隔24h收集蠶淋巴,經elisa檢測發現第4天表達量最高,根據egf標準曲線計算蠶淋巴的表達量約32 g ml ; elisa定性實驗還發現正常蠶也存在與egf抗體間交叉的物質。
  6. The expression conditions of e2 gene in p. pastoris were optimized, the results indicated that the peak obtained after 72 hours ; pattern of inhibition / induction could improve expression level ; the best ph value were between 7. 5 and 8. 0 and the optimized methanol - induced concentration was 2 % - 3 % the e2 genes of the prevalent strain ( guangxi yulin strain ) and c strain derived from rabbit spleen tissue were amplified and cloned into e. coli the expression vector pproex - htb respectively, the recombinant plasmids pproex - gxyl and pproex - c were obtained and then were transformed into the dh5a e. coli competent bacteria respectively, the recombinant bacteria could express the major antigen region of e2 gene, the expression yields amount to 35 % and 38 % repectively

    豬瘟病毒ez基因的原核表達: pcr擴增出當前豬瘟流行野毒株,國豬瘟兔化弱毒( c株)兔脾組織毒ez基因的主要抗原區,將其克隆到原核大腸桿菌表達載體pproex htb誘導表達,經sds page檢測表明,重組質粒能表達ez基因主要區蛋白, westernblot檢測表明,誘導表達蛋白與豬瘟陽性發生特異性,表達量為3538 ,可用於基因工程診斷抗原。
  7. Bleeds were taken from all mice 2 weeks after each immunization. then we assayed the influenza virus specific antibody and the ratio of igg1 to igg2a in mice serum

    每次免疫后尾部采,檢測的流感病毒特異抗體抗體的iggi / iggza比值,以確定免疫的主要類型( thz / thl ) 。
  8. In immuno - blotting, these fragments reacted specifically with hepatitis c patients " sera, suggesting that e. coli - derived e2 proteins carried hcv e2 - specific, glycosylation - and - conformation - independent epitopes

    在免疫印跡檢測,上述片段與丙型肝炎病人有特異性,表明大腸桿菌系統表達的e2蛋白攜帶有hcve2特異的、不依賴于糖化立體構象的抗原決定簇。
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