血型檢定 的英文怎麼說
中文拼音 [xiěxíngjiǎndìng]
血型檢定
英文
blood group determination- 血 : 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...
- 檢 : Ⅰ動詞1 (查) check up; inspect; examine 2 (約束; 檢點) restrain oneself; be careful in one s c...
- 定 : Ⅰ形容詞1 (平靜; 穩定) calm; stable 2 (已經確定的; 不改變的) fixed; settled; established Ⅱ動詞...
- 血型 : [醫學] blood group; blood type: abo 血型系統 abo blood group system血型分類 typing of blood; 血型...
- 檢定 : docimasy; docimasia; verification; calibration; appraisal檢定報告 probation report; 檢定滴定管 [...
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The result showed that the homology rate of pila gene among the 5 avian pathogenic e. coli strains tested and one human e. coli were from 89. 8 % to 91. 1 %, and the homology rate of amino acid were from 88. 5 % to 91. 8 %. the homology rate of pila gene sequence among 5 avian pathogenic e. coli strains tested and avian pathogenic e. coli reported ( serotype o1, o2, o78 ) were from 87. 8 % to 90. 2 %, and the homology rate of amino acid were from 84. 6 % to 91. 2 %. there had homology in avian pathogenic e. coli. there had some common antigen side in type 1 pili of avian pathogenic e. coli
結果表明:運用msha法檢測1型菌毛的檢出率為80 ( 36 45 ) , pcr法的檢出率為95 . 5 ( 43 45 ) , pcr方法用於1型菌毛的檢測比msha更加敏感、快速、特異性強;選擇5株優勢血清型雞源致病性大腸桿菌代表株( o _ ( 89 ) , o _ ( 119 ) , o _ ( 141 ) , o _ ( 127 ) )的1型菌毛pila基因的pcr擴增片段經純化后,分別定向克隆到puc18質粒的多克隆位點,構建了含有目的基因片段的克隆質粒,並轉化到dh5株大腸桿菌載體菌中,篩選獲得陽性克隆菌株。In this paper, 45 e. coli strains isolated from chicken farms in sichuan province were determined to be the pathogenic e. coli by animal test. type 1 pili of 45 strains isolated was detected by msha. the pila gene of 45 avian pathogenic e. coli strains were amplified by the polymerase chain reaction ( pcr ) with primers designed according to the sequence of the pila gene in genbank. results showed that pcr was more sensitive, faster and more characteristic than msha to detect type 1 pili
本研究將從四川規模化雞場分離鑒定、經1日齡雛雞致病性試驗得到的雞源致病性大腸桿菌45株,採用d -甘露糖敏感血凝試驗( msha )檢測1型菌毛,根據genbank中公布的人源大腸桿菌1型菌毛pila基因序列設計一對引物用pcr擴增雞源致病性大腸桿菌1型菌毛pila基因。Methods the serum hbv markers hbv dna levels in serum and pbmcs, were quant.
方法220例慢性乙型肝炎患者進行乙肝標志物檢查血清hbvdna定量及pbmcs中hbvdna檢測pcr方The organization cuts into slices and examines by the in situ pcr, drip protease k 20 ( xl with loomg / ml to digest respectively in pretreatment, increase with normal position positive cell account for total ratio of cell, according to the positive standard cells > 75 %, confirm the lightest digestion time, studying the influence and relationship of different fixation time with protease digesting each other, detecting the mn genotype of the organize slices at the same time
石蠟切片進行原位pcr檢,預處理分別滴加loom歲血的蛋白酶k20閃消化,以原位擴增顯色后陽性細胞占總細胞的比值> 75 %為標準,確定最適消化時間『 , ,研究不同固定時間與蛋白酶消化的相互影響和關系,同時檢測石蠟切片的mn基因型。Levels of fasting blood glucose and 24h urinary microcontent of albumin 24 h malb were determined dynamically ; the serum glycosyl hemoglobin hba1c was determined after the last medication ; the ultrastructural changes of kidney were observed by transmission electron microscope ; the expressions of collagen, fibronctin, laminin ln, and the ecm metabolism influencing factors, including mmp2, tissue inhibitor of metalloproteinase timp2, transfer growth factor 1 tgf 1 in renal tissue were detected by immunohistological chemistry and image collecting analytical system
動態檢測各組大鼠空腹血糖fbg 24h尿微量白蛋白24h malb ,末次給藥后測定大鼠血漿糖化血紅蛋白hba1c透射電鏡觀察各組大鼠腎臟超微結構改變,應用免疫組化技術及圖像採集分析系統測定各組大鼠腎臟組織中型膠原c纖維連接蛋白fn層粘連蛋白ln的表達,測定影響ecm代謝的基質金屬蛋白酶2 mmp2基質金屬蛋白酶抑制劑2 timp2及轉化生長因子1 tgf 1的表達。Methods according to theory of specific binding of antigen and antibody, at first the anti - a monoclonal antibody ( ma ) and anti - bma were labeled with the fluorescent, then fluorescent - labeled antibodies ( fla ) were bound with corresponding biological material ( such as bloodstain ) in the optimum condition, finally the abo blood type of bloodstain was determined under microscope fluorescent
方法根據抗原抗體特異性結合的原理,首先對抗a 、抗b單克隆抗體進行熒光標記,然後使熒光標記抗體與相應抗原(血痕)在最佳條件下結合,最後熒光顯微鏡鏡檢,判定血痕的血型。Results the fluorescent antibody method is highly sensitive, accurate and simple
結果採用該方法測定血痕的血型結果準確、靈敏度高、操作簡單、檢驗時間短。This bispecific antibody companied with another anti - p24 monospecific monoclonal antibody can build a new way of indirect rbc agglutination to detect p24 antigen, and this new way is preliminarily applied to detect serial diluted p24 to determine the sensitivity
用雙特異性抗體致敏人a型紅細胞做指示劑,以抗p24單特異件單克隆抗體9a7做交聯劑,建立間接血凝檢測p24抗原的新方法,並初步應用於檢測系列稀釋的p24抗原以確定測定的敏感性。This research use high sensitive, special in situ pcr technology to determine the material which is treated by the paraffin wax and formalin fixation of different time, by detecting the genotype of mn blood group of the organizes slices. at the same time, we study the research of main influence factors, such as protease digestion, etc. we hope to set up a kind of steady, practical methods to detect the genotype of the material treated by paraffin wax and formlin, offer a kind of new detecting means for the forensic appraises and iditificition with individual material evidence
本研究應用靈敏度高、特異性好的原位pcr技術,測定福爾馬林固定不同時間的石蠟切片組織mn血型的基因型,並對蛋白酶消化時間等主要影響因素進行了初步的研究,以建立一種穩定、實用的檢測石蠟組織切片dna遺傳標記的方法,為法醫物證鑒定和個人識別提供一種新的檢測手段。Conclusion the fluorescent antibody method is an accurate and reliable method for detection of abo blood type in biological material
結論該方法可以作為一種測定血痕血型的檢驗方法使用。The team obsered significant decreases in glucose - insulin ratio and quantitatie insulin - sensitiity check index, and significant increases in baseline insulin and homeostasis model assessment
研究小組觀察發現,血糖-胰島素比率和定量胰島素敏感性檢測指數明顯下降,而基線胰島素和內環境穩態模型評估指數明顯升高。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
每次免疫后尾部采血,檢測血清中的流感病毒特異抗體和抗體中的iggi / iggza比值,以確定免疫反應的主要類型( thz / thl ) 。Methods : in cultured lung explants without serum, the lipid component synthesis of pulmonary surfactant was evaluated in [ 3h ] - choline incorporation ; mrna content of phosphocholine cytidylyltransferase ( cct ) in lung explants was investigated in rt - pcr ; the changes of the ultrastructure of the at ii cells were observed with electron microscope ; the expression of nmdar1 subtype was observed in immunohistochemistry staining ; nitric oxide synthase ( nos ) activity, nitric oxide ( no ) content, superoxide dismutase ( sod ) level, malondialdehyde ( mda ) content and lactae dehydroase ( ldh ) level were determined by biochemistry methods. results : 1. influence of glutamate on synthesis of the lipid component of pulmonary surfactant ? with l - arginine, glu inhibited [ 3h ] - choline incorporation with good dose - dependence and time - dependence ; ( 2 ) mrna content of cct of the glu treatment groups was decreased ; ( 3 ) glu increases the release of ldh in cultured lung explants ; ( dwith electron microscope histochemistry, glu induced the changes of the ultrastruture of at ii iv cells
方法:採用成年大鼠肺組織無血清培養,運用[ ~ 3h ] -膽堿摻入法測定ps主要脂質磷脂酰膽堿( pc )合成量; rt - pcr擴增檢測肺組織中pc合成限速酶磷酸膽堿二胞苷酰基轉移酶( cct ) mrna含量;透射電子顯微鏡法觀察肺泡型上皮細胞和ps系統超微結構的變化;免疫組織化學染色檢測glu的受體nmdar1亞單位的表達;生化測定肺組織乳酸脫氫酶( ldh )釋放量和肺組織勻漿中一氧化氮合酶( nos )活性、一氧化氮( no )生成量、超氧化物歧化酶( sod )水平以及丙二醛( mda )含量。For those with family history, breast examination and mammogram could detect early breast cancer. hepatitis b carrier should follow doctor s advice on regular check of alpha feto protein and ultrasound of liver
乙型肝炎帶菌者,應依照醫生建議定期驗血液中的甲胎蛋白( afp )及接受肝臟超音波檢查,以及早察覺肝癌。Hepatitis b carrier should follow doctor s advice on regular check of alpha feto protein and ultrasound of liver. recurrent chronic stomach ulcer must be treated
乙型肝炎帶菌者,應依照醫生建議定期驗血液中的甲胎蛋白afp及接受肝臟超音波檢查,以及早察覺肝癌。In conclusion, the diagnostic methods we developed for immunological markers of hepatitis b virus by using time - resolved fluoroimmunoassay, eu - dtta as label, have wide assay ranges, high sensitivity and specificity. they would have widely application in the further research work and clinical diagnosis
總之,我們利用eu - dtta為標記物建立的乙型肝炎病毒五項血清學標志物時間分辨熒光免疫分析法分析范圍寬,靈敏度高,操作簡便,具有優越的定量檢測能力,十分適合臨床推廣應用。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
在免疫印跡檢測中,上述片段與丙型肝炎病人血清有特異性反應,表明大腸桿菌系統表達的e2蛋白攜帶有hcve2特異的、不依賴于糖化和立體構象的抗原決定簇。分享友人