硝酸纖維 的英文怎麼說
中文拼音 [xiāosuānxiānwéi]
硝酸纖維
英文
cellulose nitrate-
The colonies are replica-plated onto nitrocellulose filters.
將菌落影印接種在硝酸纖維素濾膜上。The nitrocellulose filters are then placed on wet filter paper containing alkali, which denatures the dna.
再將硝酸纖維素濾膜置於含堿的濕濾紙上，堿的作用是使DNA變性。Products include chlorides, oxides, iodide, sulfate, and nitrate, as well as ayurvedic and homeopathic formulations
-生產和經營硝酸鈉硫酸銨，依康酸，聚丙烯睛基碳纖維等基礎化工原料。This experiment passing to grope for the carbon source constitutes of the culture medium and using t. reesei rut c - 30 induced the expression of # - mannanase ( # - 1, 4 - mannan mannohydrolase ec 3. 2. 1. 78 ). in this experiment i put the constant carbon source ( lactose and locust bean gum ) in the foundation culture medium ( mandels nourishment liquid ) of t. reesei rut c - 30, then proceeded the variable carbon source ( dragon spruce fiber, com rush pith fiber, wheat straw fiber, wheat straw xylan, corn rush pith xylan, dragon spruce mannan ) to single factor, double factor, three factor, four factor and five factor orthogonal experiment. 1 determined the activity of p - mannanase using locost bean gum as substract by the 3, 5 - dinitosalicylic acid method, and observed the growing situation of the gernic at the end i selected the directions for the inducement expression of the # ? mannanase from trichoderma reesei rut - c30 that contained the dragon spruce fiber, wheat straw xylan, dragon spruce mannan
在里氏木霉rutc - 30的基礎培養基（ mandels營養液）中加入固定碳源乳糖和槐豆膠，然後將可變碳源（雲杉纖維、玉米芯纖維、麥桿纖維、麥桿木聚糖、玉米芯木聚糖、雲杉甘露聚糖）進行單因子、雙因子、三因子、四因子、五因子的里氏木霉rutc - 30正交培養實驗，並以槐豆膠為底物用3 ， 5二硝基水楊酸法測定培養液中?甘露聚糖酶的活力。從而確定了酶活最高且菌體生長良好的含雲杉纖維、麥桿木聚糖和雲杉甘露聚糖的誘導培養基為最佳培養基，用該培養基培養的里氏木霉（ t . reesei ） rutc - 30使其轉錄的-甘露聚糖酶（ - 1 ， 4 - mannanmannohydrolaseec3 . 2 . 1 . 78 ） mrna量能夠滿足rt - pcr的要求。Standard guide for soluble nitrocellulose base solutions
可溶性硝酸纖維素基溶液的標準指南Results showed that in the water body of xizi lake, annual average of culturable planktonic ammonifiers and nitrogen fixers were 510 and 236 cfu / ml, respectively ; ammonia oxidizers, nitrite oxidizers, nitrate reducers and denitrifiers were 8. 5, 16, 587 and 16 mpn / ml, respectively ; inorganic phosphate solubilizing bacteria ( 1pb ) and organic phosphorus mineralizing bacteria ( opb ) were 89 cfu / ml and 37 mpn / ml, aerobic and anaerobic cellulose decomposers were 7 and 5 mpn / ml, respectively
水體中可培養異養細菌（氨化細菌）和固氮菌的年平均值分別為510和236cfu ml ，氨氧化細菌、亞硝酸氧化細菌、硝酸鹽還原菌和脫氮菌的數量分別為8 . 5 、 16 、 587和16mpn ml ；無機磷和有機磷分解菌分別為89cfu ml和37mpn ml ；好氧性纖維素分解菌和厭氧性纖維素分解菌只有7和5mpn ml 。The capture of the labeled antibody ? analyte complex for signal generation can be achieved with the antibody immobilized in a defined area of nitrocellulose membrane as mentioned
對產生信號的標記抗體抗原復合物的捕獲，是用抗體固定在已經提到的硝酸纖維素的特定區域內來達到的。Dab served as chromagen. western blot thirty micrograms of protein extracted from untreated and bfgf, atra - induced mmscs cultures were separated on a 8 % gradient acrylamide gel and eletrophoretically transferred to a nitrocellulose membrane. the blot was probed for nse expression
4westernblot檢測誘導后細胞的nse表達情況從未經處理和經過bfgf ， atra誘導的細胞中提取30爬蛋白在8的sds一聚丙烯酸胺凝膠上電泳並轉移到硝酸纖維素膜上， 4 5脫脂奶粉封閉過夜。Standard test method for dilution ratio of active solvents in cellulose nitrate solutions
硝酸纖維素溶液中活性溶劑稀釋比的標準試驗方法The diaphragm had the ability to detect the positive serum when it was diluted to 2 ' 11 and so it has good sensitivity ; stored at 4 for at least 7 months, the sensitivity and specificity of the diaphragm did not change, so it has good stability ; when 10 positive serum was detected 3 times, the result is reproducible, so the diaphragm has good reproducible. serums from experimental inoculated piglets was detected. the results showed that when the titer is l : 16, the pigs were infected with streptococcus suis ; and when 1 : 64, the pigs could survive after challege with streptococcus suis. all the results have shown that dot - ppa - elisa was a convenient, rapid, sensitive specific useful method for the detection of antibody
該法以硝酸纖維素膜為固相載體，包被膜載抗原製成的診斷膜片具有良好的特異性：不與仔豬副傷寒、豬巴氏桿菌病、豬大腸桿菌病、豬衣原體病、豬瘟、豬細小病毒病、豬偽狂犬病、豬布氏桿菌、豬丹毒陽性血清反應；膜片具有良好的靈敏性，陽性血清作2 ~ （ - 11 ）稀釋亦能檢出；膜片具有良好的穩定性，在4至少能保存7個月，其靈敏性不變。Storage and handling of cellulose nitrate motion - picture film
硝酸纖維電影膠片的存儲和處置Preparation of alkyd resin modified waterborne nitrocellulose emulsion
醇酸改性硝化纖維素水乳液的制備研究A cellulose nitrate used as a component of smokeless powder
火纖維素硝酸纖維素，用於無煙的炸藥的組成物質The nitrocellulose filters are then placed on wet filter paper containing alkali, which denatures the dna
再將硝酸纖維素濾膜置於含堿的濕濾紙上，堿的作用是使dna變性。Standard test method for quantitative determination of cellulose nitrate in alkyd modified lacquers by infrared spectrophotometry
用紅外線光譜測定法對醇酸天然漆中硝酸纖維素定量測定的標準試驗方法We did the same steps for three times, so we could get the extraction using the steps mentioned. laemmli sample buffer was added to the extracted protein, which were then boiled for 5 min. the protein samples were separated by 12 % sds - page and transferred to nitrocellulose membrane
樣品蛋白經12 % sds一聚丙烯酞胺凝膠電泳分離后，轉印到硝酸纖維素膜上，與第一抗體4孵育過夜，經tbs洗滌后，再與第二抗體室溫孵育2小時， ttbs充分沖洗后，顯色觀察。[ methods ] two phage - epitope libraries were screened with two anti - vegf neutralizing monoclonal antibodies - jh121 and vg189, the clones were tested by dot blotting and elisa
並通過硝酸纖維膜斑點印跡法進行陽性克隆鑒定。 elisa分析陽性噬菌體克隆與抗體的親和力。Cellulose nitrate disc
硝酸纖維質唱片Radiation sensitive films ; cellulose nitrate film ; terminology, properties, utilization, storage
輻射敏感膠卷.硝酸纖維膠卷.術語特性用途貯存The high titer specific ndrg2 antibody is indispensable to reseach deeply the functions or the tissue and subcellular distribution features of ndrg2, ha order to prepare ndrg2 antibody, the whole ndrgl sequence was cloned into prset - a vector and two truncated sequences of ndrg2 were cloned into pgex - 4t - l vector. after induced by iptg, the fusion proteins were expressed in e. coli ; rabbits immunized with the whole length ndrg2 protein were reinforced with two shortened fragments of ndrg2 ; after immunization, rabbits produced high titer antiserum against ndrg2. then antisemm was absorbed using ndrg2 antigen immobilized on nc filters, the purified product of antiserum shows high special to ndrg2 protein, and the separated inclusion body of 6his - ndrg2 will be useful for the further reseach
為制備高效價的ndrgz抗體，分別構建了prset a雌、 pgex4t d唾倉和pgex4tl七三種原核重組表達質粒，並在大腸桿菌中誘導表達出相應的融合蛋白；用全長gstjqdrgz蛋白免疫兔，然後用gst ndrgz人和gstjqdrgze片段加強免疫，經免疫得到了較高效價的兔抗人ndrz多克隆抗血清，利用固定於硝酸纖維素膜上的ndrgz抗原親和吸附純化抗血清，提高了ndrgz抗體的特異性；並對包涵體形式表達的6his ndrgz進行初步的分離純化。分享友人