血原質 的英文怎麼說
中文拼音 [xiěyuánzhí]
血原質
英文
hematogen-
Conclusion the hypertensive and hyperoximic arterial blood could damage the venous endothelial cells after the vein was arterialized if the flap was transplanted after the damaged endothelial cells recovered, the survival rate and the quality of the flap could be increased remarkably
結論靜脈動脈化后高壓、高氧動脈血流可損傷靜脈內皮細胞，如先將靜脈原位動脈化，待損傷的靜脈內皮細胞修復並適應動脈血流后再行皮瓣移轉，可明顯提高皮瓣成活率及成活質量。The diabetes coronary heart disease high reason of incidence of a disease is many - sided, yet chiefly is the fat supersession chaos, and creates glycerine three grease and the cholesterol to get higher, that sweet and protein are metabolized oddly be able to create myocardium capillary pathological changes and the myocardium supersession chaos, but the flora nervous system chaos easily arouses that blood vessel pulling force adds and injures the artery breastwork
糖尿病冠心病發病率高的原因是多方面的，但主要是脂肪代謝紊亂，造成甘油三脂和膽固醇增高，糖和蛋白質代謝的失常會造成心肌的微血管病變和心肌代謝紊亂，而植物神經系統紊亂易引起血管張力增加而損傷動脈壁。In the substantial requirements of marriage, there are some common points such as the approval of the two parties concerned and monogamy principal. however, there are differences in the legal age of marriage, the range of the collateral relatives by blood who are prohibited to marry and the diseases that forbid marriage
在結婚的實質要件方面，兩地有一些共同要件，如男女雙方合意、符合一夫一妻制原則，但在結婚的法定年齡、禁止結婚的旁血親屬范圍和禁止結婚的疾病等方面存有差異。The results showed that icn formed a spatial three - dimensional structure consisting of collagenous fiber connection among myocardial, capillary and endocardium, which extensively distributed in four patterns of “ lattice ” ， “ root ”, “ shortcut ” ， and “ intracellular ”
結果顯示，心肌間質膠原網路結構在心肌、毛細血管及心內膜間以4種方式廣泛分佈，即「框格式」聯接， 「樹根樣」聯接，直接聯接和細胞內聯接。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，釉附在膠原纖維上，少量血管內皮細胞浸入基質；術后34周，無細胞真皮基質內較多的血管形成，故可認為無細胞真皮基質免疫原性低，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After selecting the pilot households in summer and autumn last year, mr. bazil fritz, a long - term program expert from canadas department of agriculture agriculture and agri - food canada stationed in inner mongolia, launched a series of work activities : monitoring the grassland, conducting training workshops for herders, training workshops for management of small - sized businesses, helping the herders to select good breeds of animals, teaching the herders how to keep records of production, establishing an effective animal identification system, testing of float grass and finding out the minerals deficient in animals according to the tested float grass, etc. a years hard work finally pays off, bringing a satisfactory result
去年夏秋季選好了示範牧戶之後，駐內蒙古長期專家巴茲爾.弗瑞茲先生開展了一系列工作：從進行草原監測，牧民培訓班，小企業管理培訓班，幫助牧民選擇優良種畜，教會他們如何做好生產記錄到幫助他們建立起一套有效的牲畜身份識別體系乃至水草檢測及根據所檢測水草配出牲畜所缺的礦物質等。一年的心血也最終換來了喜人的成果。In this paper, first strand cdna of 3abc gene was synthesized using template rna extracted from cells infected with fmdv. the complete 3abc gene about isoobp was amplified by pcr and ligated into pgem - t easy vector. after transforming e. coli dh5 a, ampicillin resistant colonies were isolated and plasmid dna was prepared and analyzed by restriction analysis and pcr. presence of the full length 3abc gene was verified by nucleotide sequence analysis and the plasmid containing the expected sequence was named as pgem - 3abc. comparing the aquired sequence of 3abc with that of reference strains, the homology is more than 99 percent. the pgem - 3abc was digested with sal i and bgl ii and ligated into xho i and bgl ii - digested expression vector ptriex - 4 neo. lt was identified by restriction analysis and pcr and sequencing that this fragment had a 17bp deletion hi the nucleotide sequence 708bp of 3abc gene, which happened to form a terminator codon behind 3ab gene, but it contained the complete open reading frame ( orf ) of 3ab gene. positive clones were selected and induced with lmmol / l isopropyl - d - galactoside ( iptg ), bacteria were detected by sds - page and western blotting after properly treated. the results showed that the 3ab gene expressed successfully in e. coli and 33. 5ku fusion protein can be recognized by the positive bovine serum of fmdv. the amount of target protein is over 26 % of the total bacteria protein by gel thin layer scanning analysis
擴增產物連接到pgem - teasy載體中，轉化大腸桿菌dh5菌株，篩選氨芐青霉素抗性菌落，提取質粒經酶切鑒定、 pcr分析以及確證性測序證明，所克隆的1500bp左右的片段含有完整的3abc基因，與國外參考序列相比，同源性在99以上。將重組質粒pgem - 3abc和表達載體ptriex - 4neo分別用sal和bgl與xho和bgl消化后，亞克隆3abc基因至原核表達載體ptriex - 4neo中，通過酶切鑒定、 pcr擴增以及序列分析，發現克隆到ptriex - 4neo載體上的片段於3abc基因708bp處出現了17bp的缺失，碰巧在3ab基因后形成一終止密碼子，但3ab基因的閱讀框架完整，選出含有3ab基因完整閱讀框架的陽性克隆，用iptg誘導表達，收集菌液進行sds - page電泳、 westernblotting分析，結果表明， 3ab基因在大腸桿菌中成功表達，其表達產物為分子量33 . 5ku的融合蛋白，並能被口蹄疫病毒陽性血清識別。經薄層掃描分析，表達量占總蛋白量的26以上。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。Abstract : fdp has many actions for mice, such as antifatigue, antioxygen - deficient, decreasing urinary nitrogen output of fatigue mice, improving glycogenesis and decreasing glycogen consumption
文摘:福達平（ fdp ）對小鼠具有抗疲勞、耐缺氧、降低疲勞小鼠血清中尿素氮質量濃度、促進糖原儲備、降低糖原消耗等作用。: the raw materials of this dish are the cores of greengrocery and the oxtail. these two materials are good for your kidney
原料菜膽和牛尾。牛尾含有豐富的蛋白質和脂肪，有益氣血、強健筋骨、補腎等功能。菜膽翠綠，牛尾軟爛、香味醇厚。The quantity and quality of hematoblast in umbilical cord blood ( ucb ) can be compared with bone marrow. furthermore, it has other advantages : widely sourced, no contamination of pathogeny, weakly antigenicity, and no mature lymphocyte, et al
臍血中造血細胞的數量和質量都與骨髓相近，而且，具有來源豐富、無病原體污染、抗原性弱、淋巴細胞不成熟等優點。Study on the electrochemical behaviors of artemisinin qinghaosu and its derivatives reduction mechanism of artemisinin in the presence of hemin
青蒿素及其衍生物的電化學性質研究氯化血紅素存在下的青蒿素還原機理Expression of thermostable direct hemolysin gene of vibrio parahaemolyticus in e. coli and activity of expressed product
副溶血性弧菌直接溶血毒素基因的原核表達及產物的性質Some blastspores even can expanded, germinated as time went on. the cockroach restrained the blastospores by phagocytosing and nodulation, and many of them melanized 5d postinfection
注射誘導后血淋巴蛋白質最明顯的變化是一些原有蛋白質濃度發生改變，如88k蛋白質顯著增加，而42k蛋白質含量減少等。The second part, a renewable piezoelectric immunosensor is developed for the antibody of schistosoma - japonicum ( sjab ). after incubating 32 kd molecular antigens of schistosoma japonicum ( sjag ) on the qcm by applying the immobilization above, the nonspecific sites on the immunosensor are sealed by using bsa and nrs together. the immunosensor can detect the sjab with the linear range of 0. 54 ~ 32. 50 ug / ml
以感染兔血清為檢測對象，採用聚電解質吸附固定法，將日本血吸蟲分子抗原（ siag32kd ）固定於石英晶振表面，再以牛血清白蛋白（ bsa ）和正常兔血清（ nrs ）聯合封閉晶振上非特異性活性位點，可在0 . 54 32 . 50ug ml范圍內檢測感染兔血清中日本血吸蟲抗體。The protein - storing cells in swietenia macrophylla were found to be populus - type, i. e. ordinary parenchyma cells containing both vacuolar protein inclusions and starch grains
用21kda蛋白質的抗血清進行兔疫印跡分析表明， 18kda蛋白質和21kda蛋白質有相同的抗原決定簇。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。Such examples are given as the blood filtering principal of hemoglobin, catalysis of enzymes, immune recoglization, prion, glycoprotein and the relationship of structure and function of membrane protein, et al, as well as the applications to medicine
在簡要介紹結構生物學的研究方法的基礎上，主要從分子水平闡述蛋白質和核酸的結構原理、相互作用、結構與功能的關系，通過具體實例闡述血紅蛋白的輸氧機制、酶的催化機制、免疫分子識別、朊病毒、糖蛋白、生物膜的結構功能關系等，以及結構生物學在醫學上的應用。Human bone morphogenetic protein 3 is a member of tgf - b superfamily. lt can induce the differentiation of cartilage and bone tissue in mesenchymal cell. and is important to bone self - repairment and bone development during embryo morphogenesis. in addition, some other biological activities of hbmp - 3 have also been found. such as inducing development of embryo and stimulating differentiation of neural and blood cells. therefore, there is a great prospect in the use of hbmp - 3. there is trace content of hbmp - 3 in human body. it has been expressed in the expression system of eukaryotes and prokaryotes respectively, but its application is restricted because of defects in the process and modification after translation in prokaryotic cells and higher costs and lower yields existed in eukaryotic expression system
人骨形成蛋白3 （ hbmp - 3 ）屬于tgf -超家族的一員，可以誘導間充質細胞分化為軟骨和骨，在胚胎時期骨骼發育和骨再生修復中起著重要的作用，而且對胚胎發育過程中中胚層的誘導和分化、造血組織的發育以及神經系統的發育和修復等都起著重要作用，因而hbmp - 3有廣闊的市場前景。它在人體內含量極微，盡管研究人員已經在原核細胞和真核細胞表達系統中分別進行了表達，但是由於原核表達系統缺乏翻譯后的加工修飾，真核表達系統存在成本高、產量低等特點，限制了其在臨床上的應用。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。分享友人