血型物質 的英文怎麼說

中文拼音 [xiěxíngzhí]
血型物質 英文
blood group substance
  • : 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...
  • : 名詞1 (東西) thing; matter; object 2 (指自己以外的人或與己相對的環境) other people; the outsi...
  • : Ⅰ名詞1 (性質; 本質) nature; character; essence 2 (質量) quality 3 (物質) matter; substance;...
  • 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...
  • 物質 : matter; substance; material
  1. 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,無細胞真皮基與周圍組織緊密枯附,盾晰葉辯;術后卜周,包埋的基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,少量管內皮細胞浸入基;術后34周,無細胞真皮基內較多的管形成,故可認為無細胞真皮基免疫原性低,能誘導宿主的成纖維細胞、巨噬細胞浸入生長,為一種新的真皮替代。第四部分無細胞真皮基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
  2. Chemist walter mccrone identified the substance as a combination of red ochre and vermilion tempera paint ; others have specifically identified it as type ab blood, with no evidence of any artificial pigments

    化學家沃爾特認定是由赭色和朱紅色的蛋彩畫顏料塗上去;其他人特別是把它鑒定為ab,沒有任何人造色素的跡象。
  3. This paper expounds the progresses of the researches on the life science and relevant subjects, which include the research of cultivating the arterial vessel with fine cell tissue, the research on the genetically modified animal, the research on the pest control with bio - virus pesticide, the research on the death mechanism of protein and the diseases of immune system ( including cancer ), the research on anti - senile protein and the research on compound - type aids vaccine

    闡述了生命科學及其相關學科的研究進展,包括用細小細胞組織培製成動脈管的研究、轉基因動的研究、生病毒農藥防治蟲害的研究、蛋白死亡機理及免疫系統疾病(包括癌癥)的研究、抗衰老蛋白的研究以及復合艾滋病疫苗的研究。
  4. Corporate system is a typical form of the modern enterprise system ; it is the result of modern market economy and the large - scale socialized production. because of the limited risk and the unlimited benefit, it greatly stimulates the investor ’ s enthusiasm and strongly promotes the development of contemporary society. corporate capital is the “ blood ” on which a company should live, the material base for management of a company, and property foundation for a company ’ s responsibility

    公司制度是現代企業制度的典形態,是現代市場經濟和社會化大生產的產,它以投資者風險責任的有限性和資產受益的無限性極大地刺激了投資者的積極性,快速地推動當代社會的發展;公司資本是公司賴以生存的「液」 ,是公司經營的基礎和公司對外承擔責任的財產基礎;現有法定、折衷和授權三種資本制,英國、美國等實行授權資本制,德國、日本、韓國等最初實行法定資本制,因實踐中存在的問題越來越多,先後改法定資本制為折衷資本制;近年來,就實施何種公司資本制度最有利於公司的發展成為大家關注的問題,學者們眾說紛紜,並沒有達成一致意見。
  5. Result : the layers of tissue engineeringed vascular model were combined tightly. hvec, vsmc and fibroblast can secrete extracelluar matrix ( ecm ) and interchange substance, resemblin physiological functions

    構建后的管模,層與層結合緊密,內皮細胞、平滑肌細胞及成纖維細胞分泌細胞外基,相互進行交換,類似於生理條3第四軍醫大學碩士學位論文件。
  6. A novel aqueous two - phase system can be formed by the mixtures of a polymer and cationicanionic surfactants. such a system can be used as a partitioning system of proteins. in this work, we investigated the formation, phase behavior and protein partitioning in aqueous two - phase systems formed by dodecyltriethylammonium bromide / sodium dodecylsulfate / peg and dodecyltriethylammonium bromide / sodium dodecylsulfate / dextran. the ligands with affinity were attached to the polymers and the affinity partitioning of proteins was investigated. it was shown that the surfactants and polymers are enriched in different phases of aqueous two - phase systems. phase separation are promoted by increasing temperature and adding inorganic salts. different proteins are partitioned in different phases. the selectivity of protein partitioning is increased by adding ligands with affinity

    報道了由正負離子表面活性劑與高聚混合溶液形成的一種可用於蛋白的分離及分析的新雙水相萃取體系.研究了正負離子表面活性劑(溴化十二烷基三乙銨/十二烷基硫酸鈉)分別與葡聚糖和聚乙二醇混合雙水相體系的形成規律、相行為及牛清蛋白和溶菌酶在雙水相體系中的分配.通過在高聚分子中接上親和配基,研究蛋白在雙水相體系中的親和分配.結果表明,在該體系中,表面活性劑與高聚分別富集於不同相中.升高溫度及加入無機鹽均可促進雙水相體系的形成,不同蛋白可分配于不同的相中.親和配基的引入極大地增強了蛋白分配的選擇性
  7. The results showed that the predominant host animal of dayangshu district was apodemus agrarius, and presently it has changed to the mixed type of hfrs

    結果表明,大楊樹地區的疫源地性是黑線姬鼠為主要宿主動的腎綜合征出熱自然疫源地,目前已演變為姬鼠為主的混合疫區。
  8. 3 antimicrobiol substance and protein in the hemolymph of nymphae induced by m. anisopliae no antimicrobiol substance was detected in the hemolymph of nymphae by different kinds of micropathogens after injection with m. anisopliae, which meant that the fungus could not induce p. americanna to produce antimicrobiol substance. injection of fungal spores caused the decline of protein concentration ( pc ) at the begaining, but after that the pc increased rapidly

    3綠僵菌孢子對蜚蠊淋巴中抗菌及蛋白的誘導注射綠僵菌后的不同時期提取蜚蠊淋巴,以多種不同類的植病原菌、昆蟲病原菌及腐生菌作為檢測菌,均未檢測出蜚蠊淋巴中有抗菌存在,即綠僵菌不能誘導蜚蠊產生抗菌
  9. 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清培養,運用[ ~ 3h ] -膽堿摻入法測定ps主要脂磷脂酰膽堿( 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、超氧化歧化酶( sod )水平以及丙二醛( mda )含量。
  10. The treatment of extensive deep burn wound is mainly by transplantation of razor - thin graft or split - thickness skin autograft in clinic. but the lack of dermis makes the wound heal with scarring and contraction. we can prepare a new kind of acellular dermal matrix ( adm ) by the method of naoh - maceration. first the acellular dermal matrix became vascularized within 3 weeks after implantation into full thickness skin defects in sd rats, then auto - split - thickness skin was overlaid on it. by animal experiments, we observed that the new kind of composite skin can reduce scarring and contraction of transplantation of razor - thin or split - thickness skin autograft

    目前在臨床上治療大面積深度燒傷的方法是移植刃厚或斷層自體皮,但因缺乏足夠的真皮成分,常造成疤痕和攣縮,本實驗用naoh消蝕法研製出一種新的真皮基( adm ) ,先將其移植于全厚皮膚缺損的大鼠背部創面,外覆蓋輻照豬皮保護3周,使其管化,再在其上移植斷層自體皮,經動實驗我們觀察到這種新復合皮膚,可以減少單純移植刃厚或斷層自體皮造成疤痕和攣縮。
  11. Methods using biocompatible alginate as microsphere material and hemoglobin as drug model, protein - loaded microspheres were prepared by an improved technology based on electrostatic droplet generation via designing components of gelation solution

    方法以生相容性優良的海藻酸鹽為載體材料,以紅蛋白為藥,通過設計凝膠浴配方,採用靜電液滴形成工藝制備包封蛋白的微球載體。
  12. Li hong et al. expression of hyluronan receptors cd44 and rhamm in stomach cancers and their relevance with tumor progression. int j oncol, 17 : 927 - 932, 2000

    李宏等:小鼠野生和突變透明酸受體rhamm的抗清制備和初步應用。中華微生學和免疫學雜志, 19 : 54 , 1999 。
  13. Sds - page and westen - blotting validated the expression of pp24. the expressed specific band was excised from the gel and injected into mice once two weeks for 5 times, then we collected the antiserum from the mice and used it for ifa with chicken embryonic fibroblasts ( cef ) infected by mdv mdll, cvi988 and ga strains respectively. the positive straining was found in the mdv plaques, which shows the in vitro expressed protein of pp24 has some epitopes of mdv

    mdvmd11株的pp38基因和pp24基因的完整orf分別克隆入真核表達載體pcdna3 . 1 / zeo ( + )中,重組粒pcdna3 . 1 - pp38和pcdna3 . 1 - pp24在脂體作用下分別轉染cef ,在轉染后24 、 48 、 72小時,用單抗h19和pgex - pp24原核表達產制備的抗清分別對pcdna3 . 1 - pp38和pcdna3 . 1 - pp24轉染的cef進行ifa檢測,結果檢測到了pp38和pp24在cef中的表達,該試驗也使pp24基因在原核和真核系統中的表達得到了相互驗證。
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