acid binding 中文意思是什麼
acid binding
解釋
酸接合-
Recently, ldl apheresis has been applied in clinic and achieves a satisactory effect. in this dissertation, the tripeptide, serine - aspartic - glutamic acid ( sde ), which existes in the cooh - terminal end of the seven repeats in the ligand binding domain of the ldl receptor and plays an important role in identifying ldl, was synthetized and immobilized onto the polyacrylamide ( paam ) beads as a bionic adsorbent for selective removal of ldl from plasma
本論文以絲氨酰-天冬氨酰-谷氨酸（ sde ）負電性三肽（此三肽廣泛存在於ldl受體配體結合域7個重復序列的羧基末端，對ldl受體特異性識別ldl起著重要作用）作為配體固定到聚丙烯酰胺微球載體上製成仿生性ldl親和吸附劑，考察其對人血漿中ldl及hdl的吸附功效。 -
Our previous studies showed existence of apoplast cam in the plant cell and cam had many extracellular functions. so it supposed cam may be one of important extracellular polypeptides and trigger the intracellular signal transduction by binding the receptor. in this study, radiolabelled ligand is used to investigate the binding characteristic of cam and a. thaliana protoplasts. and chemical crosslinking is employed to explore binding proteins in the membrane. at first, ( 35 ) ~ s - cam was produced using ( 35 ) ~ s - labeled amino acid mixture in e. coli. sds - page and autoradiograph indicated high - purified, high - specific radioactivity ( 35 ) ~ s - cam was obtained. electrophoresis of ( 35 ) ~ s - cam is the same as that of unlabeled cam with ca ~ ( 2 + ) or egta ; a quatitive of protoplasts was prepared by enzymolysis
首先，用~ （ 35 ） s標記的氨基酸混合物喂養工程菌成功地制備了~ （ 35 ） s標記的擬南芥鈣調素（ ~ （ 35 ） s - cam ） ， ~ （ 35 ） s - cam純度高、放射活度高、 ca ~ （ 2 + ）與egta存在時的電泳行為與未標記cam相同，可作為一種高靈敏性的探針用於進行受體學分析實驗；用擬南芥種子誘導愈傷，通過酶解制備了大量原生質體。 -
Researches of schistosomiasis vaccines have gone more than 60 years, approximately including from the stages of dead vaccine and live vaccine ( irradiated attenuated cercariae vaccine ) to gene engineered vaccine, etc. many different forms of vaccines have been tested in animal models, including gluthathione s - transferase, paramyosin, irv - 5, triose phosphate isomerase, sm23, fatty acid binding protein ; which were considered promising by who / tdr. but none of them steadily accomplished the pre - set target level of 40 % protection. in order to enhance the protective capacity further, it is essential to develop novel vaccine antigens and / or vaccine adjuvants
血吸蟲病疫苗研究已有60多年的歷史，大致經歷了死疫苗、活疫苗（照射致弱尾蚴疫苗）和基因工程疫苗等研究階段，產生了一些who / tdr推薦認為很有希望的疫苗候選分子，如谷胱甘肽- s -轉移酶（ gst ） 、副肌球蛋白（ sm97 ） 、照射致弱疫苗抗原5 （ irv - 5 ） 、磷酸丙糖異構酶（ tpi ） 、曼氏血吸蟲膜內在蛋白（ sm23 ）和脂肪酸結合蛋白（ fabp ， sm14 ）等，但其對宿主的保護作用均不甚理想，未能穩定地達到40或以上的保護力水平，因此有必要繼續尋找新的疫苗抗原分子和/或疫苗佐劑，進一步提高其保護力。 -
The results show that the chemosensor exhitits selective fluorescent quenching in the presence of aromatic organic acid in acetonitrile solution, and that the binding ability of the chemosensor with organic acid is in the order of p - cyanic - benzyl acid > p - chloric - benzyl acid > p - methoxyl - benzyl acid > benzyl acid
結果表明，所合成的熒光分子在乙腈溶液中能選擇性識別芳香族有機酸，表現出熒光淬滅現象，其與有機酸絡合能力的大小依次為：對氰基苯甲酸對氯苯甲酸對甲氧基苯甲酸苯甲酸。 -
Main methods and results are as followed : 1 epitope analysis of agonist - binding region of nrla physicochemical properties and antigenicity of two agonist - binding regions of nrla were analyzed through bioinformatics : domain p1 containing 151 amino acid residues preceding the first transmembrane domain of the human nrla, domain p2 with 144 residues following the third transmembrane domain. four parameters including hopp - woods and kyte hydrophilicityjanin accessibility, karplus - schulz flexibility, and welling antigenicity were used to determine the antigenic sites, and prosite programme and chou - fasman method were employed to analyze their related sequence motif and the secondary structures
用goldkey軟體分別選取公認的hopp等與kyte等親水性參數、 jain表面可及性參數、 karplus - schulz主鏈柔韌性參數及welling抗原性參數對p1 、 p2兩個多肽片段進行參數分析。並採用通用的prosite程序與chou - fasman方法比較分析p1 、 p2多肽片段的氨基酸位點與二級結構特徵。綜合判定兩個多肽片段的抗原性及其位點，結果認為p2抗原性強于p1 。 -
Hyaluronic acid, as acid mucopolysaccharide, fulfils important tasks in the connective tissue ; it plays an essential role in the regulation of water binding capacity, supports the regulation of the distribution of plasma proteins and promotes wound healing
透明質酸，作為一種粘多糖酸，在結締組織中有著非常重要的作用，它是調節組織水合能力的關鍵，同時改善血漿蛋白的運輸和促進傷口愈合。 -
The most commonly used method for the covalent binding of biomolecules onto 1 - d nanostructures is through the diimide - activated amidation of carboxylic acid terminated nanostructures
最常用的方法是通過端羧酸基納米結構的二酰亞胺活化氨基化合物來進行生物分子與1 - d納米結構的共價結合。 -
Results show that vp37 protein can bind single strand nucleic acid cooperatively and nonspecificallty, and the vp37 - ssrna complex was stable at high salt concentrations, suggesting vp37 is a possible mp. vp37 is the only protein characterized so far showing rna - binding ability in genus fabavirus
為了驗證vp37是否具有核酸結合能力，我們利用6his - vp37蛋白進行了核酸結合實驗，結果表明vp37是一種能非特異性結合單鏈核酸的蛋白；其在結合核酸時具有協同性； na ~ +的變化對其核酸結合能力影響較小。 -
To guide the cam - binding peptide into apoplast space, the signal peptide from brassica campetris pollen coat protein slr1 ? ps was employed. it has total 26 amino acid, and is a very classic form of signal peptide
為了把cam結合小肽帶到質外體，本實驗選擇了野生蕓苔屬植物（ brassicacampetris ）花粉胞壁蛋白slr1 - bps的信號肽。 -
A page gel, stained by the petiodic acid - schiff ' s method to reveal glycoproteins, further displayed that the bindng - protein was a glycoprotein belonging to lectin, which contained 17. 4 % ( w / w ) neutral carbohydrate content of the glycoprotein detected by the phenol / h2so4 method. peptide mapping was comparable to the reported protein in protein bank. the database homology search ( ncbi blast ) indicated that the binding - protein shared 70 - 80 % homogeneity to l - aspartate oxidase, aspartyl / glutamyl - trna ( asn / gln ) amidotransferase subunit b, glutamyl - trna reductase, histidyl - trna synthetase
連續梯度聚丙烯耽胺凝膠電泳、 sds一聚丙烯酞胺凝膠電泳和等電聚焦的結果表明該蛋白分子量為1 「 . skda ，由二個相同的亞基組成，亞基分子量為」 . ikda ，等電點為8 . 25 .糖蛋白染色結合考馬斯亮藍染色的結果證實此結合蛋白是個糖蛋白，其中糖含量為17 . 44 % ，蛋白含量為82 . 56 % .凝集反應確定該糖蛋白也是一個凝集素 -
Edta ethylenediamine tetra - acetic acid, a compound that acts as a chelating agent, reversibly binding iron, magnesium, and other positive ions
學名為乙二胺四乙酸，是一種具有螯合作用的化合物，能夠可逆地結合鐵離子、鎂離子以及其他正離子。 -
Genetic variants at heart fatty acid - binding protein loci in hubei white pigs
心臟型脂肪酸結合蛋白基因多態性在湖北白豬中的初步研究 -
Ie acts as a general gene transcription activator. it consists of dna - binding domain and acid amino acid transcription activate domain. what kinds of promoter can be stimulated by ie 180
另外ie180與hsv的立即早期蛋白icp4有較大的同源性，研究ie180轉錄調控作用有利於皰疹病毒轉錄調控模型的建立。 -
By elisa analysis, inhibition of binding of clq with the c ! q receptors on u937 cells and competitive inhibition of binding of clq with aggregated immunoglobulin g b y selected phage clones, and dna sequencing, a number of similar, but not identical, sets of sequences of clq - binding clones were identified. the deduced amino acid sequences of selected 9 peptides are wyegpftlytwp, hwdpfslsayfp, ltqhnspffllp, tsnpfflwypqp, qtpfqlw, npfnwts, spfxlts, fltwldp and fstflyp. they show significant efficiency to inhibit the binding of clq with the clq receptors on u937 cells and / or aggregated immunoglobulin g, which suggest that the selected peptides contain the modeling epitopes of clq receptor to bind the collage - like region or igg to bind the head domain of clq
然後，採用噬菌體肽庫技術，以c1q為釣餌蛋白，從12肽庫和環7肽庫中親和篩選能與c1q結合的噬菌體克隆，經elisa 、 u937細胞配體結合抑制試驗、 aigg競爭抑制試驗及dna測序，獲得了9個具c1q抑制活性克隆的dna序列，其相應的氨基酸序列為： wyegpftlytwp 、 hwdpfslsayfp 、 ltqhnspffllp 、 tsnpfflwypqp 、 qtpfqlw 、 npfnwts 、 spfxlts 、 fltwldp 、 fstflyp ，它們可能模擬c1qr和或igg的c1q結合表位並抑制c1q的活性。 -
Rflps at heart and adipocyte fatty acid binding protein genes in beijing oil chick and aijiao chick
脂肪型脂肪酸結合蛋白基因多態性的研究 -
The krupple type zinc finger motif found in many transcription factors is thought to be important for nucleic acid binding and / or dimerization. here we have identified and characterized two novel zinc finger genes named znf323 and znf360 using degenerate primers from an early human embryo heart cdna library
本文利用kr ppel型（ cys _ 2 his _ 2型）鋅指基因順序上的保守特徵，設計簡並引物從人類早期胚胎cdna文庫中初步篩選克隆出四個kr pple型鋅指蛋白新基因，經國際基因命名委員會批準命名為znf323 、 znf360 、 znf359和zfp28 。 -
Recently an abscisic acid binding protein with high specificity and affinity for aba was purified from epidermis of vicia faba l. in our laboratory, and further characterized using various biochemical techniques, there is evidence to link the protein to the physiological effects of aba in some aspects. the above - mentioned work may result in the molecular cloning the gene encoding aba binding protein
近年來，我室利用親和層析從蠶豆下表皮中分離出一種高親合、高度特異性的aba結合蛋白，並完成了對其生化特性深入分析及部分測序，且在一定程度上揭示了該蛋白與aba的生理功能效應存在著內在的聯系，這為進一步克隆aba結合蛋白基因奠定了堅實的工作基礎。 -
Cloning and sequencing of fatty acid binding proteins gene in chicken
雞脂肪酸結合蛋白基因的克隆和測序分析 -
The screening on affinity ligand of heart - type fatty acid - binding protein
心肌型脂肪酸結合蛋白特異性親和配體的篩選 -
Cloning and sequencing of heart fatty acid - binding protein gene in porcine
豬心臟脂肪酸結合蛋白基因的克隆和測序分析
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