酶刺激作用 的英文怎麼說
中文拼音 [cìjīzuòyòng]
酶刺激作用
英文
enzyme stimulation-
The enzyme cholinesterase is important in the transmission of nerve impulses.
膽堿酯酶在神經刺激的傳導中起著重要作用。The extracted marrows ganoderma lucidum and semen zizyphi spinosae contained in threesss can regulate secretion of hydrocortisone in human body and reduce excitation of human body during nighttime ; in addition, ganoderma - lucidum spores and semen zizyphi jointly stimulate secretion of sleeping - inducting peptide in body. improve rate of " high efficient sleeping quality and immunity. recover and strengthen mental strength, mental strength and vigor. through sleeping. the psychlogy and physiology return to the youth level
「索萊爾」多元明膠囊中所含的靈芝和酸棗仁提取精華，能調節人體內皮質醇的分泌，降低人體在夜間的興奮度；此外靈芝孢子粉和酸棗仁共同作用，能夠在體內刺激「睡眠肽」和格里酶「的分泌，有效促進「高能睡眠」率，延長「高能睡眠」時間，從而達到全面改善睡眠質量，提高免疫力，使體力、腦力、精力得到迅速恢復和加強，通過睡眠將生理及心理狀態調整到青春期水平。The effort of manganese removal was studied and the kinetics of manganese removal was tried to establish. the factors of dissolved oxygen concentration, fe2 + concentration, ph, p concentration and closing of the filter were studied to evaluate their effort for biological manganese removal, and the correlation of residual manganese and oxidation - reduction potential was also discussed. as the iron content of water was high, experiment results showed that the reaction was zero order, as the iron content of water was low, the reaction was first order. the time needed for the cultivation of biological manganese removal was 60 70 days. the filter operated at the filtration rate of 8 10m / h, silica sand of effective size 0. 95 1. 25mm filled the filter to a depth of 1200mm
試驗結果表明，成熟后濾砂表面濾膜的x射線衍射圖譜與mno _ x ? 5h _ 2o （ x = 1 . 86 ）的x射線衍射圖譜一樣，濾膜成熟后的結構在進水物質不發生變化的情況下不發生變化;合適的碳磷比對生物除錳有明顯的促進作用，試驗條件下的投磷量不會對出水造成二次污染;生物除錳需要亞鐵的參與，亞鐵的存在除了能夠促進微生物分泌胞外酶並刺激其活性外，還通過鐵離子的變價傳遞電子，催化錳離子的氧化反應，從而促進對二價錳的降解。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。The elicitor of this pathway is ca2 +, ca2 + binds to sos3, which leads to interaction with sos2, a ser / thr protein kinase of 446 amino acids, and activated the kinase. the transcription and post - transcription of sosl, an putative na + / h + antiporter on the membrane is controlled by the sos3 - sos2 complex
這條途徑的起始為外界高鹽刺激使細胞內ca ~ （ 2 + ）水平發生變化， ca ~ （ 2 + ）作為第二信使與sos3結合，然後導致sos3與sos2相互作用激活sos2的激酶活性，形成sos2 - sos3激酶復合體。The combination of meja and fc did not show significant additive effect on enzyme activity. 3. phosphorylation and dephosphorlation of pm h ^ - atpase after treatments of meja and fc 1 ) in vitro, phosphatase inhibitors, okadaic acid and cantharidin, enhanced meja - induced increase of the enzyme activity to 60 % and 50 %, respectively
Tllrase過程中可能發生的磷酸化和去磷酸化作用1 ）磷酸酶抑制劑斑螫素、崗田酸可以增強meja對酶的刺激作用，崗田酸的效應較強，而斑鰲素的作用略弱，增幅分別為60和50左右。There was no difference in other biologic characteristic of mscs between the two separation method, such as cell anchorage ratio and clone formation ratio. ( 2 ) plga film presented uniformity frame with no protuberance and fissure under scanning electron microscopy ( sem ). big aperture with smooth wall and average 400 m i n size running - through each other was observed in porous plga substrate, around the big aperture there were many round micropores about 5 m size. all of the structure were equal and uniform, which satisfied the further research work. ( 3 ) mscs adhesion at earlier time was promoted by biotiegenrafter 3h, cell number was ( 1. 5 0. 18 ) 105 in the plga film coated with biotiegen group, which was significantly higher than that in plga film group ( p < 0. 01 ) and higher than that in coverslip group ( p < 0. 05 ), which cell number was ( 1. 04 0. 21 ) 105. after 6h and 12h biotiegen could not promote cell adhesion, and cell proliferation and alkaline phosphatase ( alp ) activity were not promoted dramatically during 9 days. ( 4 ) cell adhesion was promoted by fibronectin or collagen type i
G ） i型膠原、纖維粘連蛋白促進細胞增殖，細胞接種后3 、 6 、 gd三個檢測時間點，實驗組細胞均明顯高於對照組。與1型膠原相比，纖維粘連蛋白刺激作用更強。 ） i型膠原、纖維粘連蛋白尚能誘導mscs細胞向成骨細胞分化，不僅表達成骨細胞標志物ocn 、 alp 、 opnmrna ，而且堿性磷酸酶活性明顯增高，堿性磷酸酶及鈣結節7第四軍醫大學博士學位論文一染色均強陽性， i型膠原組mscs細胞堿性磷酸酶活性較fn組更高，有顯著性差異；同時，兔疫組化染色表明，經纖維粘連蛋白作用的mscs1型膠原表達陽性。In the present study, in order to investigate the effects of endogenous estrogen on the daergic terminals in amy and the daergic neurons in midbrain, fast cyclic voltammetry ( fcv ) was used to examine da release evoked by electrical stimulation from amy of female rats in different phases of estrus cycle, ovx rats and male rats. and tyrosine hydroxylase ( th ) immunohistochemi stry was employed to measure the numbers of daergic neurons of ventral tegmental area ( vta ) and substantia nigra ( snc ) in the rats
因此，為進一步探討大鼠內源性雌激素水平的變化對amyda能神經系統及中腦da能神經元的影響，本工作應用快速周期伏安法（ fcv ）在體監測了處于動情周期各期雌鼠、 ovx鼠和雄鼠經電刺激誘發的amyda釋放，並應用酪氨酸羥化酶（ th ）免疫組化方法測定了以上各組大鼠腹側背蓋區（ vta ） 、黑質（ snc ）的th陽性神經元數目。Phopholipase c - 1 ( plc - 1 ) is widely known to play an important role in regulating cell proliferation and differentiation, development of the organisms, cell transformation and oxidative stress. till now, the mechanism how phopholipase c - 1 acts can not be thoroughly illustrated, nor has the interaction between plc - 1 pathway and other signal pathways been systematically reported. this research chose 2 - de + ms as the basic method from all kinds of proteomics strategies and compared the total protein expression map of mef genetically deficient in plc - 1 ( plc - 1 - / - ) to that of wild type mef ( plc - l + / + ) aimed to find some protein spots differentially expressed, thus we can discuss the impact of knockout of plc - 1 on signal transduction initiated by growth factors such as egf comprehensively. in this way, we can study the biological function of plc - 1 and mechanism of plc - 1 pathway indirectly, which will contribute a lot to further analysis
鑒于plc - 1發揮上述作用的機制尚未完全闡明， plc - 1通路與其他信號通路間的交聯和代償尚無系統報道，又因為以往的研究方法不夠全面，本研究以野生型小鼠胚胎成纖維細胞（ plc - 1 ~ （ + / + ） ）和缺失磷脂酶c - 1的小鼠胚胎成纖維細胞（ plc - 1 ~ （ - / - ） ）為研究模型，在眾多蛋白組學策略中選擇了雙向電泳+質譜（ 2 - de + ms ）作為研究手段，通過對比表皮生長因子（ egf ）刺激24小時後上述兩種細胞的總蛋白質表達差異，全面地探討敲除plc - 1對生長因子誘導的信號傳遞的影響，從而間接研究plc - 1生物學作用、信號傳遞機制及其代償情況，為后續的深入研究打下基礎。Staurosporine and cheleythrine, two inhibitors of protein kinase, inhibited the stimulation of meja on pm h + - atpase activity completely. 2 ) both protein kinase inhibitors and phosphatase inhibitors showed the same effect on fc - induced increases of enzyme activities
二）崗田酸和斑鰲素對fc刺激酶活力的作用有增強，增幅分別為60和50 ；蛋白激酶抑制劑星形抱菌素和白屈菜紅堿則可完全抑制fc對酶的刺激作用。The levels of stimulation by 10 u mol / l meja in vitro also showed about 30 % increase of the enzyme activity 2hr after incubation of membrane vesicles with
離體實驗表明： 10nmol l的meja處理zhr對質膜h 「 atpase的刺激作用最強，酶的水解活力增加約30 。Extension of low k + treatment to 12 hours did not increase the binding sites or protein abundance either. among ros species, h2o2 was specifically involved in the up - regulation of na, k - atpase induced by low k. 96 base pairs of upstream of na, k - atpase subunit promoter was the key cis - element in transcriptional regulation of promoter activity
Ros對鈉鉀atp酶亞基啟動子的刺激作用縮小至編碼區上游96堿基對，該序列包含多個潛在sp1轉錄因子結合位點，研究也表明sp1參與了低鉀對鈉鉀atp酶的調節作用。分享友人