p-protein 中文意思是什麼

p-protein 解釋
p-蛋白
  1. Two protein peaks can be obtained by bio - gel p - 6 chromatography and both peaks have antimicrobial activity. so the bacteriocin is consisted of two proteins with different mw. only one protein with larger mw can be detected through tricine - sds - page, and its mw is about 8, 570da

    採用30硫酸銨就能完全把發酵液中的細菌素全部沉澱，通過生物膠bio - gelp - 6層析發現細菌素被分離出兩條抗菌蛋白峰，這表明r21 - 4產生的細菌素是由兩種不同分子量的蛋白質組成的，通過tricine - sds - page檢測，只能檢測到一條分子量相對較大的細菌素，分子量在8 ， 570da左右。
  2. Results the treatment group was superior significantly to the control group in the field of reduction of serum total bilirubin, the total bile acid, the total effective rates, advance of prothrombin activity ( pta ) and alph fetal protein ( afp ) of chronic fulminant hepatitis and the effective rates of the treatment group ( p < 0. 05 )

    結果治療組在降低血清總膽紅素、總膽汁酸、升高凝血酶原活動度、維持較高血清甲胎蛋白水平、提高存活率等方面均優于對照組，差異有顯著性（ p < 0 . 05或0 . 01 ） 。
  3. The results show that the algaecides can react with the chlorophyl a, the protein and the sod enzyme, and also can destroy the modality of the algae. soluble chitin - iodine was also discussed. the results show that soluble chitin - iodine can remove the p. globosa red tide

    通過研究碘伏、新潔而滅和異噻唑啉酮對棕囊藻的生理效應和使用掃描電子顯微鏡觀察棕囊藻的形態結構的破壞情況，探討了這幾種除藻劑的除藻機理。
  4. Sedegah m, hedstrom rc, hobart p, et al. protection against malaria by immunization with plasmid dna encoding circumsporozoite protein [ j ]. proc natl acad sci usa, 1994, 91 ( 21 ) : 9866

    劉彥文，余新炳，徐勁等.惡性瘧原蟲海南株環子孢子蛋白基因的克隆與表達[ j ] .中國人獸共患病雜志， 2000 ， 16 （ 1 ） : 8
  5. The highest vt and p valt in true leaf were accompanied two hybridizable polypeptides of aox protein, 35kd and 38kd respectively. the next was cotyledon vt and p valt with only one 38kd hybridizable polypeptide of aox protein. hypocotyl vt and p valt were the lowest and its immunobloting band was similar to that of cotyledon, but the expressive amount of 38kd protein was less than that of cotyledon

    綠豆幼苗不同器官的有關呼吸參數測定結果與aox表達的western分析基本一致：真葉的v _ t特別是v _ （ alt ）最高，它也具有35kd和38kd的aox的雜交多肽；其次是子葉的v _ t和v _ （ alt ） ，且在子葉中，只見一條分子量為38kd的aox多肽；下胚軸的v _ t和v _ （ alt ）都最低， western雜交顯示也只有一條分子量為38kd的多肽，而且表達量也較少。
  6. Study on interaction between p - hydroquinone and cattle serum protein

    對苯二酚與牛血清白蛋白相互作用研究
  7. Linearized the expression vector ppic9k - p including the truncated mutant pokeweed antiviral protein ( pap ) gene by restriction endonuclease sal i and transformed it electrically into pichia pastoris gs115. mut + recombinants were selected by pcr and high yield mut + recombinant was picked out by double film immunoblotting

    本研究將含有n末端信號肽和c末端毒性區缺失的pap基因的表達載體ppic9k - p用sali酶切線性化后，通過電擊轉化整合p . pastorisgs115菌株細胞中。
  8. Egfr mrna and protein levels in jar were significantly higher than those in normal trophoblast ( p < 0. 01 )

    妊高征組egfllin wa的表達也明顯低於對照組呼功
  9. Vanadate, a potent ptpase inhibitor, locks adipocyte differentiation at an early stage in the program and leds to the accumulation of p - c - crkii, a phosphotyrosyl protein that is a substrate for ptpase ha2

    研究發現一種強烈的磷酸酯酶抑制劑- -釩酸鈉能夠作用於脂肪細胞的分化早期過程從而抑制其分化，並使一種ptpha2的底物即酪氨酸磷酸化的蛋白質p - c - crkii累積。
  10. Effect of p, p ' - dde on androgen binding protein gene expression on sertoli cells of rat

    對睪丸支持細胞雄激素結合蛋白表達的影響
  11. Ability to a - complement of the ea / ed protein was determined by the addition of onpg western blot test with rabbit to e. coli p - galactosidase pcab as first antibody was used to verify the fusion proteins

    以兔抗p半乳糖昔酶抗體做western blot以證實與gst融合表達的ea工d蛋白是p半乳糖昔酶的成分。實驗結果1
  12. To search proteins that associate with the mouse mint protein and regulate notch signaling in nuclei, and to study the function and mechanism of mint - mediated transcription repression, yeast two - hybrid assay was used to screen proteins that interact with a fragment of mint ( f5, amino acids 2226 - 2959 ). from 4x106 yeast clones transformed with the bait plasmid and a cdna library of 9 dpc mouse embryo, fifty - one were positive for nutritional screening and p - galactosidase assay. restriction digestion identified 10 independent positive clones and these were analyzed by dna sequencing these clones represent 3 correctly fused cdna fragments, which are mint, alpha a - crystallin - binding protein i ( alphaa - crybpl ), and nuclear receptor co - repressor 1 ( n - corl ), respectively

    鑒于mwt基因編碼區較長，共有10799個堿基，故此我們將mint分為六段，分別命名為fi一f6 ，本研究以其中的f5 （ 222e959 ）和f6 （ 296s576 ）片段為研究對象，將h者分別插入pgb盯7載體中，結果顯示： mintfs可與核受體輔助抑制因子1階cori ） ， o晶狀體蛋白結合蛋白1hlphatcrybp入及mw加互作用，而f6可與igm的重鏈恆定區、泛素結合酶2l6和一個未知功能的新的蛋白基因進行結合。
  13. The expression efficiency difference between ped5 and pcdhfrl, a vector utilizing cmv enhancer / promoter ( pcmv - ie ) for foreign protein production, was analyzed using human interferon - p ( ifn - ) gene and human secreted alkaline phosphatase ( seap ) gene as reporters. when analyzed in transient expression, ped5 showed a little more protein produciton than pcdhfrl. however, in continuous expression, when serum concentration was lessened to slow down cell proliferation, ped5 expressed 3. 1 times more reporter proteins than pcdhfrl, which implied that pef - io was less affected by cell cycle status in contrast to pcmv - ie, making ped5 a good expression vector for foreign protein production

    應用人-干擾素（ ifn - ）和人分泌型堿性磷酸酶（ seap ）基因作為報告基因，對含有巨細胞病毒即早期啟動子（ p _ （ cmv - ie ） ）的表達載體pcdhfr1和ped5表達外源蛋白的能力進行了比較，發現對于瞬時表達， ped5略好於pcdhfr1 ；在穩定表達中，通過降低血清濃度，使細胞增殖緩慢，這時ped5表達外源蛋白的能力較pcdhfr1高3 . 1倍。
  14. We succeeded in constructing the fusion protein plasmids of ea and ed of p - galactosidase. 2

    構建的質粒能高效表達具有較高a一互補活性的gs …蛋白、 gsthd蛋白。
  15. Rt - pcr results suggested ha94 was a late gene. western blot analysis of extracts of hasnpv - infected hzaml cells revealed a specific protein of 43 kda from 48 h to 96 h p. i.

    Rt - pcr結果表明ha94是一個晚期基因，在感染后24小時開始檢測到病毒的轉錄產物，持續到表達至96小時。
  16. In the research of transgenic fish, green fluorescent protein gene was sub - cloned to downstream of carp p - actin gene promoter that was cloned in pucusa by molecular recombination technology. thus pagfp plasmid was constructed successfully. the recombination was determined by digestion of restriction enzyme and sequencing

    實驗通過分子重組技術，採用定向克隆法將綠色熒光蛋白基因亞克隆到puc118a上鯉魚-肌動蛋白基因啟動子下游，構建成能在真核生物體內表達的表達載體pagfp ，經雙酶酶切法序列鑒定后，回收帶啟動子和目的基因片段。
  17. The transparent rings formed by bacterium decomposing protein between flesh - eating bugs and plant - eating bugs were different. the former were wider than latter. 3. the ratio of amylase to protease enzyme activies ( a / p ) was used as one of the criteria for identifying the feeding habits of bug. the a / p for plant - eating bugs was about 2. 0 - 6. 0, for the flesh - eating bugs was 0. 3 - 0. 8

    3試驗採用-澱粉酶活力蛋白酶活力比值作為指標，對蝽類昆蟲進行了食性鑒定，結果表明：肉食性蝽類的-澱粉酶蛋白酶比值范圍在0 . 3 0 . 8之間，而植食性蝽類的-澱粉酶蛋白酶比值范圍在2 . 0 6 . 0之間，食性差異明顯。
  18. In n terminal, 3 conserved sequences, wxixgmxgxgkttla, l ( i / v ) ( v / l ) lddv ( w / d ) and sriixttrd xxv are in term of p - loop, kinase 2 and kinase 3a. those are highly identical to the homologous of human ( apaf - 1 ) and namenode ( ced - 4 ). it revealed that tm - 22 encodes a membrane protein with a receptor structure and kinase property and may function in ion flow, phosphorylation and proteins interaction

    Tm一夕基因的編碼蛋白在該區與tm一2有32個氨基酸的差異，主要集中在第10 、 11和12個亮氨酸重復序列中，與tm一2有兩個氨基酸的差異，僅僅是位於第12個亮氨酸重復序列中的767和769兩個位點，這表明:第一， lrr是tm一22基因和tm一2基因編碼蛋白對病毒識別的特異區段;第二， 767和769兩個位點的差異氨基酸是tm一22基因和tm一2基因編碼蛋白對病毒識別的特異位點。
  19. The recombination expression vector, ppic9 - e2, was linearized by sal i and electroporated into p. pastoris gs115. recombinant p. pastoris gs115, designated gs115 - ppic9 - e2, was identified by pcr and the product of the pcr was analyzed by sequencing before its expression for csfv e2 protein

    重組表達載體ppic9 - e2經sal酶切線性化后，電轉化整合到畢赤酵母gs115基因組上，經pcr鑒定和pcr產物測序分析，陽性轉化子命名為gs115 - ppic9 - e2 。
  20. Based on the actual biology settling, kinesin moves along microtubule which is constructed from asymmetrical o and p protein subunits which array periodically, so the microtubule ' s structure is also asymmetrical and periodical. during the motion, kinesin ' s configuration changes in a dynamic - chemical period in which there are several dynamic - chemical states for the motor, and the transitions are random between state and state to a certain extent

    根據實際的生物背景，驅動蛋白沿微管作定向運動，構成這些微管的蛋白亞基順序排列，形成非對稱的周期性結構，且驅動蛋白在運動過程中構象發生了變化，在一個力學和化學循環中要經歷多個中間態，各個態之間的躍遷具有隨機性。
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