血蛋白計 的英文怎麼說

中文拼音 [xiědànbáijì]
血蛋白計 英文
haemagiobinometer
  • 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...
  • 蛋 : 名詞1. （鳥類或龜、蛇類所產的卵） egg 2. （像蛋形的東西） an egg-shaped thing 3. （辱罵之詞）
  • 白 : Ⅰ形容詞1 （似雪的顏色） white 2 （清楚; 明白; 弄明白） clear 3 （空的; 沒加他物的） pure; clear; ...
  • 計 : Ⅰ動詞1 （計算） count; compute; calculate; number 2 （設想; 打算） plan; plot Ⅱ名詞1 （測量或計算...
  • 蛋白 : 1. （卵中透明的膠狀物質） egg white; albumen; gary2. [生物化學] （蛋白質） protein
  1. After careful studying their relative importance to immune response and the possibility of the match, seventeen sequences of interest were selected for further experiment, including estss analogous to 11. 5kd antibacterial peptide, lysozyme, serine protease and its inhibitor, lectin, antifreeze protein, et al. primers designed according to the sequences were used to amplify the corresponding estss from both blood and cephalothorax cdna library

    在仔細分析了它們在免疫系統中的重要性和在對蝦中出現的可能性之後，從中選出了17條可能編碼抗菌肽，溶菌酶，凝集素、絲氨酸蛋白酶及其抑制劑，抗凍蛋白等蛋白質的序列，以此為依據設計引物，在中國對蝦的血液和頭胸部cdna文庫中擴增相應的序列。
  2. We launched an integrated designing experiment to isolate, purify and identify a protein from a tissue, we also set up a designing experiment isolating - globin from serum

    開設蛋白質分離、純化、鑒定的綜合性實驗，並開設了設計性實驗從血清中初步分離-環蛋白，由學生自己查找原理和方法、自己設計實驗步驟、自己動手實施，並且用獲得的樣品進行精細分離和鑒定。
  3. Lenis explains the basic concepts of how to create non - toxic meals ( this type of cooking is sometimes called slow food or low temperature cooking ) then goes to the kitchen where everyone gets a hand on experience of how to make delicious foods that are quick, easy, and healthy. you will also learn the basics of nutrition including eating for blood sugar and metabolism regulation ( key for weight control ), protein and carbohydrate requirements, healthy fat intake, vitamin and mineral requirements, calorie counting methods, understanding the effects of alcohol, identifying sources of toxins, and many important subjects for healthy nutrition

    您也會學習到有關于營養的基本知識，包括能控制體重的血糖和新陳代謝機制的飲食方法、蛋白質和碳水化合物、健康脂肪、維他命及礦物質的正確攝取量，和計算熱量的方法，並且能夠理解酒精對人體的影響、認識毒素的來源還有許多有關于營養健康的議題。
  4. 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疫苗，將sp17和cyritestin關鍵表位和牛核糖核酸酶非選擇性th細胞表位合理組合，獲得新抗原- 35肽序列；並在合成、純化後分別與弗氏佐劑、免疫刺激復合物（ iscoms ）混合后免疫不同遺傳背景的雌性小鼠，觀察血清和生殖道內的特異性抗體滴度的動態變化、生育力的改變以及免疫后小鼠重要臟器的組織病理學改變：以及在ivf下，新抗原的特異性抗血清對精卵相互作用的影響及抗原在精子表面的特異性定位。
  5. Since fibrinogen is derived from human body, the physician must evaluate the risk that serum hepatitis may follow its use

    由於「纖維蛋白原」來自人血，醫生必須估計到使用本品后可能引起血清肝炎的危險性。
  6. 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

    實驗中將蛋白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，計算出免疫反應的親和常數為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，應用此傳感器成功地對5種癌癥病人血清中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。
  7. The serum creatinine, blood urea nitrogen, triglyceride and low density lipoprotein decreased significantly in the jpqhr - treated group as compared with those in the control group ( p < 0. 05 ), while the number of erythrocyte rosette - forming cells increased significantly in the jpqhr - treated group as compared with those in the control group ( p < 0. 05 )

    結果：健脾清化方組患者的臨床癥狀有明顯改善，血肌酐、尿素氮、甘油三酯和低密度脂蛋白均有下降，而紅細胞總花環有顯著增加，與對照組比較，有統計學意義（ p < 0 . 05 ） 。
  8. 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

    通過細胞的免疫組化，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。免疫組化結果顯示：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血清，成蟲蟲體可溶性抗原免疫兔血清， ts87基因原核表達蛋白免疫兔血清（ ts87血清）以及一株具保護性的旋毛蟲單抗特異識別。
  9. Microbiology of food and animal feeding stuffs. horizontal method for the enumeration of coagulase - positive staphylococci staphylococcus aureus and other species. part 2 : technique using rabbit plasma fibrinogen agar

    食品和動物飼料微生物學.凝膠水平計數方法.陽性葡萄球菌和其它屬.第2部分:兔原生質血纖蛋白質瓊脂培養基技術
  10. Stepwise discriminant analysis was performed to obtain risk factors of caa based on clinical and early laboratory data

    我們先以單變數統計方法來檢驗十六個臨床和實驗變數，發現在兩群中只有白血球和c -反應蛋白質具有統計上之顯著差異。
  11. Systematic cluster analysis was carried out on hu sheep in china in comparison with the same data of 9 asia sheep populations and 5 european sheep ( breeds in japan ) populations. 15 populations can be clustered in terms of gene frequency of 10 loci and 33 allele in blood enzyme and other protein variations

    摘要以中國湖羊為研究對象，搜集國內外9個亞洲綿羊群體和5個在日本的歐洲綿羊群體的相同資料作為對照，根據控制血液酶和其他蛋白質變異的10個基因座位共計33個等位基因的頻率，進行系統聚類分析。
  12. For the identification of deer species with body parts like bone, skin, hair, muscle, visceral organ, antler, blood, embryo, and their various products, the traditional methods are not likely powerful enough to discriminate these involved samples. for establishing an effective identification methodology, keratin and mtdna polymorphisms were studied and taken as genetic markers of deer species. the methods established here were proved effective for any deer primary products

    對于鹿類動物骨骼、皮張、被毛、肌肉、內臟等組織、茸片、血液、胎兒及這些材料制備的各種產品的種屬鑒定，傳統的方法難以滿足識別鑒定的需要，本文針對這一問題，從角蛋白和dna水平上設計和建立了鹿類動物物種識別方法體系，幾乎可以用於任何鹿類初級產品的鑒別。
  13. Increased neutrocytes could he observed immediately after detection of the hematoma, but they tended to return to normal thereafter, while hemoglobin kept falling for 3 - 4 days after detection of hematoma

    血常規檢查中性粒細胞計數在發現血腫后即刻即明顯升高，但第2天開始緩慢降低並逐漸恢復正常；而紅細胞及血紅蛋白在發現血腫后持續降低，平均3 ~ 4天後才停止降低趨勢並逐漸回升。
  14. Part i this paper has minutely studied the interaction between ag ( i ) and serum albumin. the binding of ag ( i ) to human serum albumin ( hsa ) or bovine serum albumin ( bsa ) has been studied by equilibrium dialysis at ph ( 5. 4 ). the scatchard analysis indicates that there exists several strong binding sites of ag ( i ) in both hsa and bsa. a notable hysteretic effect has been observed in the interaction of ag ( i ) with hsa or bsa using uv - visible spectrometry at ph ( 5. 4 ), which shows that the binding between ag ( i ) with hsa or bsa may induce a slow transition of hsa or bsa from the conformation of weaker affinity for ag ( i ) to one of stronger affinity ( a - b transition ). the rate constants and activation parameters of this transition parameters of this tansition were measured and discussed. the binding equilibrium has been also studied by resonance light - scattering spectrum ( rls ) and flurescence quenching

    第一部分：等離子點ph （ 5 . 4 ）條件下，用平衡透析法和紫外光譜，熒光光譜，共振散射光譜研究了ag （ ）與人血清白蛋白（ humanserumalbumin ，簡稱hsa ）或牛血清白蛋白（ bovineserumalbumin ，簡稱bsa ）的結合。 scatchard圖分析表明， ag （ ）在hsa或bsa中有強弱兩類結合部位，通過計算機擬合獲得結合的逐級穩定常數值。紫外掃描發現ag （ ）與hsa或bsa的結合存在滯後效應，表明ag （ ）與hsa或bsa的結合可能誘導蛋白質構象發生緩慢變化（ a - b ） ，測得並討論了這一構象變化的速度常數和活化參數。
  15. Purpose 1 construction of prokaryotic high expression vector of human platelet factor 4 ( h pf4 ) 2 expression and purification of r h pf4 3 bioassay of r h pf4 methods according to the modulation character of eukaryotic protein expression in prokaryotic cells, we design a pair of particular primers, and construct a prokaryotic expression vector pbv220 - r hpf4 by dna polymerase chain reaction ( pcr ) and dna recombinant technic. the expression plasmid was identified with pcr and dna sequencing. pbv220 - r hpf4 was transformed into e. coli dh5a, bl21 ( de3 ) and induced by increasing the temperature to 42. we identified the expression protein by sds - page and western - blotting

    目的1人血小板因子4 （ hpf4 ）原核高效表達克隆的構建2重組hpf4的表達及分離、純化工藝研究3重組hpf4的特性研究方法根據原核細胞表達真核蛋白的基因表達調控特點，設計合成一對特異引物，在pt7 - 7 - rpf4表達質粒的基礎上，應用聚合酶鏈式反應（ pcr ）對其cdna進行改造，通過dna重組技術構建成重組hpf4原核表達質粒pbv220 - rhpf4 ，用快速pcr檢測法、 dna測序分析，鑒定重組hpf4表達質粒的正確性。
  16. Studying the significant role of transporters in drug blood - brain barrier can provide deep analysis of the drug kinetics in the blood - brain barrier transport with effective regulation and helpful for understanding the interaction between the transporters and substrate ; and furthermore with guidance to the research and development of drugs including brain - targeting and nonbrain - targeting

    對轉運蛋白在藥物血腦屏障轉運中的重要作用進行研究，可深入地解析藥物在血腦屏障上的動態並更有效地調控藥物轉運行為，有助於了解血腦屏障上轉運蛋白與底物藥物的相互作用，指導腦靶向與非腦靶向藥物的研發設計。
  17. Patients who have a negative result i. e. no troponin t in the blood, have a very good prognosis and can be safely discharged home

    如果病人測試得到陰性結果，即血液中測不到肌鈣蛋白- t ，預計病人的病程發展會很好，可以放心出院，遲些方做進一步檢查。
  18. Part ii this paper has minutely studied the interaction between au ( iii ) and serum albumin. the binding of au ( iii ) to human serum albumin ( hsa ) or bovine serum albumin ( bsa ) has been studied by equilibrium dialysis at ph ( 7. 43 + 0. 02 ). the scatchard analysis indicates that there exists several strong binding sites of au ( iii ) in both hsa and bsa. a notable hysteretic effect has been observed in the interaction of au ( iii ) with hsa or bsa using uv - visible spectrometry at ph ( 7. 43 + 0. 02 ), which shows that the binding between au ( iii ) with hsa or bsa may induce a slow transition of hsa or bsa from the conformation of weaker affinity for au ( iii ) to one of stronger affinity ( a - b transition ). the rate constants and activation parameters of this transition parameters of this tansition were measured and discussed. the binding equilibrium has project supported by the national science foundation of china ( no. 299621001 ), and the foundation for talents of the ten hunred thousand in guangxi

    第二部分：生理ph （ 7 . 43 0 . 02 ）條件下，用平衡透析法和紫外光譜，熒光光譜研究了金（ ）與人血清白蛋白（ humanserumalbumin ，簡稱hsa ）或牛血清白蛋白（ bovineserumalbumin ，簡稱bsa ）的結合。 scatchard圖分析表明，金（ ）在hsa或bsa中有強弱兩類結合部位，通過計算機擬合獲得結合的逐級穩定常數值。利用熒光猝滅法計算出金（ ） - hsa和金（ ） - bsa體系的stem - volmer常數和雙分子猝滅速率常數。
  19. Serum protein refractometer

    血清蛋白折射計
  20. Part iii the medicines about gold will be very popular in the next ten years. 25, physiologically ph 7. 43 ( + 0. 02 ), applying resonance light - scattering spectrum ( rls ), we observed the resonance light - scattering spectrum quenching of serum albumin by its interaction with au ( iii ). a scattering peak at 350nm and its double frequency scattering peak at 700nm were observed when the excited wavelenth is 290nm

    第三部分：在普通熒光分光光度計上選擇合適的激發和發射通帶寬度，利用reyleigh共振散射技術，研究了生理ph值7 . 43 （ 0 . 02 ） ， 25下，金（ ）與血清白蛋白的相互作用。
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