氯蛋白 的英文怎麼說
中文拼音 [dànbái]
氯蛋白
英文
chloralbacid-
Approach on sapk mediated the effect of cadmium chloride on apoptosis of adrenocortical cells
應激活化蛋白激酶介導氯化鎘致腎上腺皮質細胞凋亡作用探討A study on apoptosis and activity of sapk jnk in adrenocortical cells induced by cadmium chloride
氯化鎘誘發腎上腺皮質細胞凋亡與應激活化蛋白激酶活性的研究Clinical prove with the experiment, the rhizome of large - headed atractylodes can promote gastric bowel to secrete wriggle with alleviation stomach bowel, enhance diuresis, platoon sodium is chloric, increase albumin synthesis, fall blood sugar, and protective liver cell and prevent glycogen yuan reductive action
臨床與實驗證實，白術能促進胃腸分泌與緩和胃腸蠕動，增強利尿、排鈉氯，增加白蛋白合成、降血糖，以及保護肝細胞和防止肝糖元減少的作用。Conclusion the concentrations of cefoperazone sodium, chloromycetin, ciprofloxacin lactate and gentamycin sulfate showed significant influence on the coagulation time and detection rate of fibrinogen in plasma
結論頭孢哌酮鈉、氯黴素、乳酸環丙沙星、硫酸慶大黴素等抗菌素及其濃度變化對血漿中纖維蛋白原的凝固時間和檢出率有顯著影響。Methods add the cefoperazone sodium, chloromycetin, ciprofloxacin lactate and gentamycin sulfate at different concentrations into plasma and determine the coagulation time and content of fibrinogen
方法採用凝固法，以加入抗菌素后血漿中纖維蛋白原的凝固時間為指標，觀察不同濃度的頭孢哌酮鈉、氯黴素、乳酸環丙沙星和硫酸慶大黴素對血漿纖維蛋白原的影響。However, the detection rate of fibrinogen increased with the decreasing concentrations of chloromycetin, gentamycin sulfate and ciprofloxacin lactate, but decreased with the decreasing concentration of cefoperazone sodium
隨著氯黴素、硫酸慶大黴素、乳酸環丙沙星濃度降低，血漿中纖維蛋白檢出率升高；隨著頭孢哌酮鈉濃度降低，血漿中纖維蛋白原檢出率亦降低。Results the coagulation time of fibrinogen in plasma increased with the decreasing concentrations of chloromycetin, gentamycin sulfate and ciprofloxacin lactate, but decreased with the decreasing concentration of cefoperazone sodium
結果隨著氯黴素、硫酸慶大黴素和乳酸環丙沙星濃度的降低，血漿中纖維蛋白原的凝固時間延長；而隨著頭孢哌酮鈉濃度的降低，凝固時間反而縮短。The secret is engineering them to produce light - activated proteins that pump chloride ions outside of the cells, briefly desensitizing them
這項工程的秘密在於訓練它們產生一種可由光來激活的蛋白質，可以向神經元細胞外面排放氯離子，簡單地說，就是降低它們的感光性。Chlorotyrosine was not elevated in patients with high mpo or carbonyl levels
Mpo或蛋白質羰基升高的病人3 -氯酪氨酸並不升高。It is the optimal time for subjecting creatine to the medium when cultured to 12h and the concentration of creatine was 0. 75 %. creatine, sarcosine and choline chloride could induce the creatinase production and creatine was the optimal inducer, but creatinine and urea could not induce the creatinase production. 3 purification of creatinase the process of creatinase purification was performed as follows : first the enzyme was completely precipitated in the range of 40 - 80 % of saturation with ammonia sulfate fraction precipitation
最佳氮源為玉米漿和蛋白腖，最佳比例為2 ： 3 ，最佳濃度為1 . 6 ；加入其它碳源時有助於菌株穩定產酶； 100ml搖瓶的最佳裝液量為15ml ；肌酸、肌氨酸和氯化膽堿都能誘導菌株產酶，其中肌酸誘導產酶的效果最好，而肌酐和尿素不能誘導菌株產酶；誘導物肌酸的最適加入時間為接種培養12小時后，最適加入量為0 . 75 。Methods : hyperosmotic pressure animal model was established by administering 3 % sodium chloride as drinking water to rats or increasing osmotic pressure of the culture medium. osmoregulation positions in the brain, reciprocal projection pathways between the medullary visceral zone ( mvz ) and supraoptic nucleus ( son ) or hypothalamic paraventricular nucleus ( pvn ), oscillation of intracellular calcium in cultured neurons and astrocytes were studied by means of anti - fos, glial fibrillary acidic protein ( gfap ), tyrosine hydroxylase ( th ) or vasopressin ( vp ) multiple imrnunohistochemical staining, immuno - electronic microscope, wga - hrp retrogradely tracing and cell culture methods. results : ( 1 ) fos positive neurons within the mvz, parabrachial nuclei, locus ceruleus, pvn, son, subfomical organ increased markedly
方法：通過給予大鼠飲用3氯化鈉或提高培養基滲透壓濃度的方法復制高滲刺激模型，主要採用抗fos 、膠質原纖維酸性蛋白（ gfap ）和酪氨酸羥化酶（ th ） （或加壓素? vp ）免疫組織化學多重染色、免疫電鏡、 wga - hrp束路追蹤結合免疫組織化學多重染色、細胞培養等實驗方法，系統觀察了中樞參與滲透壓反射的調控部位、下丘腦視上核（ son ）神經元? ast超微結構的變化、延髓內臟帶（ mvz ）和son及下丘腦室旁核（ pvn ）之間往返投射通路和神經元的性質及其與ast的關系、培養神經元和ast內鈣波的變化。Aminated and hydroxylated polysulfone membranes were prepared by amination and hydroxylation reaction, respectively. then bovine albumin ( bsa ) - fixed membranes were obtained by crossed - linking albumin into porous membrane with 1, 1 ' - carbonyldiimidazole and bisoxirane reagents, respectively. a mathematical model for facilitated transport in asymmetric membranes with fixed site carriers was derived by assuming an instantaneous, microscopic concentraion fluctuation in the membrane
以氯甲基聚碸為基材，通過相轉化法制備出具有底部貫通孔的非對稱膜，通過胺化和羥基化反應，分別制得胺化聚碸膜和羥基化聚碸膜，再採用羰基二咪唑和雙環氧烷兩種活化試劑對其進行活化，將牛血清白蛋白固載在膜內，獲得固定白蛋白促進傳遞膜。The protein binding selectivity of clozapine was discussed
討論了氯氮平蛋白結合作用的選擇性。Manufacturer of nitrates and other inorganics in china. products include sodium, potassium, magnesium, and calcium nitrate, sodium and calcium nitrite, potassium sulfate, ammonium and potassium phosphates, and ammonium chloride
-生產銷售三氯化鋁1 ， 1 ， 1 -三氯乙烷氯化石蠟n -乙基乙二胺n -乙基雙氧哌嗪蛋白腖和硫鐵礦氟石精礦等，包括公司簡介產品介紹等Therefore, we evaluated blood pressure and proteinuria after changeover from amlodipine to benidipine in poorly controlled hypertensive patients
在血壓控制不佳的患者中，我們用貝尼地平替代氨氯地平，而後評估換藥后血壓和蛋白尿。Based on studying the performance of the acrylics - based and poly - vinyl - based milk - protein fibers, the new qualitative identification method about the two kinds of milk - protein fibers is researched with the chemical agent " zncl - i2 "
摘要在研究腈綸基和維綸基牛奶蛋白纖維的性能特徵基礎上，探索了氯化鋅碘試劑定性鑒別兩種牛奶蛋白纖維的新方法。Extraction of large - fragment genomic dna in order to gain dna template of pcr amplification ( long pcr amplification and salvage pcr amplification ) which was high purity and large fragment, three methods were used to extract genomic dna of bacillus subtilis, i. e. low melting - point agarose embedding method, sds - proteinase k - phenol chloroform extraction method and bacterial genomic dna extraction kit method. the genomic dna of bacillus subtilis were gained by these methods, and the operated programs of the methods were improved. the results showed that the genomic dna extracted by low melting - point agarose embedding method were obviously biggest than that of another two methods
大片段基因組dna的提取為了獲得用於pcr擴增（長距離pcr擴增和分段pcr擴增）的高純度、大片段（至少為pcr產物長度的4倍）的dna模板，應用三種方法：低熔點瓊脂糖包埋法， sds -蛋白酶k -酚氯仿抽提法和細菌基因組dna提取試劑盒法，分別提取獲得了枯草桿菌基因組dna ，並對3種方法的操作程序進行了不同程度的改進，結果表明：低熔點瓊脂糖包埋法提取的基因組dna片段明顯大於后兩種方法，採用0 . 5瓊脂糖凝膠電泳3h ，仍然跑不出加樣孔。According to the result showed at 280nm and at 490nm, in the comparison of whether protein absorption top and sugar quantity top overlapped, glycoproteins would be detected preparatorily, and as a result, tubes in two distinct areas had glycoproteins by this method. proteins were precipitated with trichloroaceticacid and with cold acetone, and glycoprotein was determined from sds - gel
再從各收集管的收集液中，用三氯乙酸沉澱蛋白法、冷丙酮沉澱蛋白法相結合濃縮、制備蛋白樣品，進行sds ? page ，對sds膠進行pas糖鏈染色鑒定糖蛋白，並從茶樹葉分級蛋白中準確地鑒定出兩個區域的收集管中含有多種糖蛋白。In young chickens aev induces paralysis, ataxia and muscular dystrophy, while in older chickens, infection is usually subclinical, resulting in a decline in egg production and hatchability. infectivity was shown to remain unaffected by chloroform, low ph, pepsin, trypsin and deoxyribonuclease. magnesium cations were shown to stabilise preparations of the virus against heat inactivation. the buoyant density of virions are 1. 31g / ml. the diameter of the virion was estimated to be 22 to 30nm. the aev can be adapted to grow in chicken embryo. the inability of aev to grow effeciently in most cell cultures
幼雞感染該病毒后，引起麻痹、頭頸震顫甚至共濟失調，而成雞常呈亞臨床感染或導致產蛋量和孵化率下降。病毒的感染性不受氯仿、低ph 、胃蛋白酶、胰酶和脫氧核糖核酸酶的影響，鎂離子可增強病毒對熱的穩定性，病毒的浮密度為1 . 31g ml ，直徑為22 - 30nm ，該病毒主要在雞胚中增殖，在大多數細胞培養物中不生長。Blood and urine with water or the supernatiant of viscera sample being deproteined with 6 % hclo4 solution was add 0. 2ml gdx301 porous polymer bead and shaken to absorb the drugs in specimen. then the bead was packed into a glass column. the column was washed with 10ml water and elution was effected with dichloromethane
血、尿用水稀釋，臟器用6高氯酸沉澱蛋白后，加0衛dgdx301樹脂振搖，濾集樹脂于小層析柱中，用水10inl淋洗，二氯甲烷洗脫，收集洗脫液sml ，揮干後用0分享友人