磷酸脫氧胞苷 的英文怎麼說

中文拼音 [līnsuāntuōyǎngbāo]
磷酸脫氧胞苷 英文
dcmp
  • : 名詞[化學] phosphorus (15號元素,符號p)
  • : 酸構詞成分。
  • : Ⅰ動詞1 (脫落) cast; shed; drop; fall off 2 (取下; 除去) take off; strip; cast off 3 (脫離) ...
  • : 名詞[化學] (氣體元素) oxygen (o)
  • : Ⅰ名詞1 (胞衣) afterbirth2 (同一個國家或民族的人) fellow countryman; compatriot Ⅱ形容詞(同胞...
  • : 名詞[化學] (有機化合物的一類) glucoside
  • 磷酸 : [無機化學] orthophosphoric acid; phosphoric acid磷酸胺 [化學] phosphamide; ammonium phosphate; 磷...
  1. All of our products is exported likelactobacillus acidophilus, bidifobacterium longum, lactobacillus paracasei, lactobacillus rhamnosus, tagatose, lnulin, nisin, natamycin, - polylysine, nucleotides mix, adenosine monophosphate, cytidine monophosphate, guanosine monophosphate disodium, uridine monophosphate disodium, calcium inosinate, calcium guanylate, calcium 5 - ribonucleotide, damp, dcmp, dgmp, tmp, deoxyadenosine, 2, 6 - diaminopurine nucleoside, 2, 6 - diaminopurine deoxynucleoside, adenine arabinoside, adenosine triphosphate, uridine triphosphate, guanosine triphosphate, cytidine triphosphate, cytidine diphosphate choline ( citicoline ) to all over the world, if you are interested in our products, please do visit our website, hope there will fullfill your requirement

    主營產品有益生菌(嗜乳桿菌、長雙歧桿菌、乾酪乳桿菌、鼠李糖乳桿菌) 、塔格糖、菊粉(菊糖) 、乳鏈球菌素、納他黴素、 -聚賴氨、核,腺,鳥二鈉,尿二鈉,肌,鳥鈣,核糖核鈣,,胸二鈉,二鈉,, 2 -氨基, 2 -氨基腺,阿糖腺膽堿,腺,三尿,三,三
  2. All of our products is exported like nucleotides mix, adenosine monophosphate, cytidine monophosphate, guanosine monophosphate disodium, uridine monophosphate disodium, calcium inosinate, calcium guanylate, calcium 5 - ribonucleotide, damp, dcmp, dgmp, tmp, deoxyadenosine, 2, 6 - diaminopurine nucleoside, 2, 6 - diaminopurine deoxynucleoside, adenine arabinoside, adenosine triphosphate, uridine triphosphate, guanosine triphosphate, cytidine triphosphate, cytidine diphosphate choline ( citicoline ) to all over the world, if you are interested in our products, please do visit our website, hope there will fullfill your requirement

    主營產品有核,腺,鳥二鈉,尿二鈉,肌,鳥鈣,核糖核鈣,,胸二鈉,二鈉,, 2 -氨基, 2 -氨基腺,阿糖腺膽堿,腺,三尿,三,三
  3. The routine method for inducing protein function evolution is imitating and speeding protein gene mutation. in this research - amylase gene was mutated in vitro by pcr with dntp in which deoxythymidine triphosphate ( dttp ) was partially replaced by 5 - bromo - 2 ' - deoxyuridine - 5 ' - triphosphate ( 5 - bdu ). the higher the concentration is, the stronger its inducing ability is in a certain range

    本研究採用5 -溴尿( 5 - bdu )部分取代( dttp ) ,在pcr的過程中對克隆的野油菜黃單菌的-澱粉酶基因進行了體外誘變,誘變結果表明: 5 - bdu濃度越高,誘變越強;濃度越低,誘變越弱。
  4. 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血清培養,運用[ ~ 3h ] -膽堿摻入法測定ps主要脂質脂酰膽堿( pc )合成量; rt - pcr擴增檢測肺組織中pc合成限速酶膽堿二酰基轉移酶( cct ) mrna含量;透射電子顯微鏡法觀察肺泡型上皮細和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;生化測定肺組織乳氫酶( ldh )釋放量和肺組織勻漿中一化氮合酶( nos )活性、一化氮( no )生成量、超化物歧化酶( sod )水平以及丙二醛( mda )含量。
  5. To make clear the hypothesis, a middle cerebral artery occlusion ( mcao ) and hypoxia and glucose - deprivation ( hgd ) ischemic models were used in in vivo and in vitro study, respectively. we first studied the cellular localization of kvl. 2 and the co - localization of kvl. 2 protein and vegf receptors flk - 1 and flt - 1, observed the effect of mcao on kvl. 2 expression and phosphrylation in the rat brain in vivo, then investigated the effect of vegf on ischemia / hypoxia cell damage and tyrosine phosphorylation of kvl. 2 in sh - sy5y cells. finally, in order to further elucidate the relationship between vegf ' s neuroprotection and its regulation on kvl. 2 phosphorylation, we used a specific antisense oligodeoxynucleotide ( odn ) to knockdown the expression of endogenous vegf to observe its role in ischemia / hypoxia cell damage and regulation of kvl. 2 phosphorylation

    為了驗證上述假設,本文分別在整體和離體水平,採用大腦中動脈缺血( middlecerebralarteryocclusion , mcao )和體外?糖剝奪( hypoxiaandglucose - deprivation , hgd )缺血模型,首先了解了kv1 . 2蛋白的細定位及與vegf受體flk - 1和flt - 1的共存情況,觀察了整體mcao后缺血再灌不同時間大鼠腦內kv1 . 2蛋白的化水平變化,然後通過外源性給予vegf蛋白,在sh - sy5y細株上觀察其對缺血細存活率及kv1 . 2蛋白化水平的影響,最後利用vegf反義寡核( oligodeoxynucleotide , odn )特異阻斷內源性vegf蛋白的表達,觀察內源性vegf蛋白在缺血細損傷及調節kv1 . 2蛋白化中的作用,以進一步明確vegf缺血保護效應與其調節kv1 . 2蛋白化之間的關系。
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