specific inhibitor 中文意思是什麼
specific inhibitor
解釋
特殊抑制劑-
The po is very sensitive to some trypsin - specific inhibitors such as sbti, p - apmsf and bestatin, but almost not affected by trypsin - specific inhibitor tlck at all, indicates that it is like a tyrosine - type protease
在對蝦中也已報道了一些免疫促進劑，能不同程度地提高對蝦的自身免疫力，但其具體作用機理目前還不清楚。 -
In the study, three drugs were gien to the olunteers : ssri ( serotonin specific reuptake inhibitor ) to raise serotonin leels ; nari ( noradrenaline reuptake inhibitor ) to raise noradrenaline leels ( another neurotransmitter important in depression, and also found in taste buds ) ; and an inactie placebo
在該項研究中，志願者服用的三種藥物是：提高5 -羥色胺水平的ssri （選擇性5 -羥色胺再攝取抑制劑） ，提高去甲腎上腺素（另外一種對抑鬱癥有重要作用的神經遞質，也存在於味蕾中）水平的nari （去甲腎上腺素再攝取抑制劑） ，以及無活性的安慰劑。 -
Gefitinib ( iressa, zd1839 ), a specific tyrosine kinase inhibitor that targets the epidermal growth factor receptor ( egfr ), is a novel molecular - targeting antineoplastic agent
摘要吉非替尼是一種新型的分子靶向抗癌藥物，它選擇性抑製表皮生長因子受體酪氨酸激酶而發揮作用。 -
We produce a wide variety of corrosion inhibitor papers each designed for use with a specific metal beginning with the steel - use type
以鋼鐵用途為首，提供適用於各種金屬的防銹紙。 -
But it further inhibited the low affinity system. 1. 3 effect of k + channel inhibitor on the na + content nem ( 3 mmol / l ) is a specific inhibitor of the high affinity k + uptake system
另一個是不飽和的低親和k ~ +吸收系統，其一級反應常數k為1 . 1 ，說明nacl脅迫濃度的增加進一步抑制了堿蓬的低親和k ~ +吸收系統。 -
Based on epidermal strip bioassay, microinjection, patch - clamp and laser scanning confocal microscopy in the experiments, we provided the first evidence that map kinases, including mek1 / 2 or p38 / hog1, plays an important role i n aba - or sa - induced h2o2 signal initial, amplification and specific targeting in response to stimuli in guard cells. aba - or h2o2 - induced vicia faba stomatal closure. was inhibited or reversed by the specific inhibitor pd98059 of mek1 / 2 ; the guard cells were pre - incubated or - microinjected by 10 umol l - 1 pd98059, aba could not enhance the fluorescence intensity of h2o2 probe dichlorofluorescein ( dcf )
在對照實驗中， aba誘導熒光迅速增高；單獨的pd98059 、 pd98059和aba共同處理氣孔時，保衛細胞內h _ 2o _ 2探針熒光強度沒有增高；將pd98059注射進入其中的一個保衛細胞，再以aba處理，使得兩個有同樣熒光基礎的保衛細胞熒光強度對比強烈；將pd98059顯微注射進入已被aba誘導dcf （ dichlorofluorescin ）熒光強度升高的氣孔保衛細胞，熒光強度下降，而沒有被注射一邊的保衛細胞中的dcf熒光強度不變。 -
Within the family of angiogenesis inhibitors, angiostatin, an endothelial cell - specific inhibitor, has been demonstrated to be the most potent
在血管生成抑制因子的家族中血管抑素（ angiostatin ）作為內皮細胞特異性的抑制劑已顯示出強大的作用。 -
As a potent, highly specific and reversible inhibitor for acetylcholinesterase of central nervous system, it has been proven preclinically to possess the ability to improve learning and memory in a broad range of animal models with cognitive deficits, and furthermore has been authorized for treating ad and benign memory deficits since 1994
臨床前試驗證實石杉堿甲對一系列認知障礙模型動物的學習和記憶均有改善作用， 1994年批準在國內臨床用於治療阿爾采末病和良性記憶障礙。 -
Our research show that sb203580, a specific inhibitor of p38a and p38b, at the concentration of 1umol l - 1, potentially could disrupt or reverse h2o2 - induced stomatal closing or inward k + current decreasing, besides the inhibitor partially down - regulates aba - induced stomatal closing and inward k + current lowering, but it does not reverse aba - induced inward k + current lowering. sb202474, a structurally related with sb203580 but inactive compound, does not ; and sb203580 is specifically involved in the downstream h2o2 signaling cascades in guard cells. to insight into the p38 mapk founctions in aba - and sa - induced h2o2 accumulation in guard cells, we went on resaearching the dcf fluorescence intensity by the a
3 . sb203580 、 sbzoz190分別以不同方式阻斷了aba和sa誘導的hzo :產生sbzo358o和aba共同處理時，保衛細胞中的dcf熒光強度沒有升高，而且bapta處理不影響sb203580的這一作用; sb203580注射進入保衛細胞后，胞外aba處理，兩個具有同樣熒光基礎的保衛細胞，熒光強度對比強烈;將sb203580和h20 :一起注射進入保衛細胞，再以aba處理，經過注射的保衛細胞dcf熒光強度低於沒有注射的一方; sb203580和sa共同處理時， dcf熒光仍能升高。 -
Pharmacological evidences show that quercetin - inducing hypergravitropism is structural specific activity, and the second massager such as ca2 + and camp take parts in this process, and polar auxin transport is indispensable. a conclusion can be made from all these results that quercetin, one kind of flavonoid, does not act as pat inhibitor but regulates auxin transport at the level of signal transduction in arabidopsis
藥物學實驗結果表明， q誘導超向地性來自於末端特異性結構，同時細胞內的ca ~ （ 2 + ）和camp等二級信使也參與了這一過程，並且生長素極性運輸也是發生超向地性所不可缺少的條件。
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