positive plate 中文意思是什麼
positive plate
解釋
陽極板；正極板-
Construction and expression of yeast engineering yaccine : s14 / gnsag " as transformed to yeast host straln x33 by means of electroporation after ppiczaa s, . aresag " as l ined by saci enzyme. the single fungus, as choose and dibble inocu1ating in we and am plate, the positive fungus was gro ' ing in rm but not in w, and was 6 inoculated in ypd which included zeocine 500ug / ml and 1000ug / ml. 5 transformers were ampl if ied by pcr, three is same with positive control
選取單個菌落分別點種到刪平板和md平板，找出在回d上生長正常， w上生長緩慢或不生長的菌落，即陽性菌落，再以陽性菌落分別塗布zeocine含量500ug加， 1000ug砌l的ypd平板，以高濃度的抗生素篩選高拷貝的酵母工程菌，在含500ug ml高濃度抗生素平板上獲得了15個轉化子，取其中5個進行pcr擴增，有3個擴增產物與陽性對照相同，說明此酵母細胞中已含有s hbsag融合片段，其中之一命名為p -
The distributions of current density and potential on the negative plates with the radiational or expanded grid designs are more uniform than those on the positive plate
輻射式和拉網式負極板在化成開始時電流密度和電位的分佈都比正極板上分佈均勻得多。 -
This rhomboid shaped crystal of calcium pyrophosphate, which appears bluish - white ( weak positive birefringence ) by polarized light with red plate
焦磷酸鈣菱形結晶在紅感光板偏振光下呈藍白色（弱正雙折射） 。 -
Among inorganic salts tested, k2hpo4was more essential to the sclerotia formation and carotenogenesis of strain pt9s than kcl, mgso4 or feso4 it was also shown that the combination of k2hpo4, kcl and mgso4 could produce the best positive cooperation and give the highest sclerotia biomass ( 782mg / plate ) and pigment yield ( 328 g / plate ). all of five carbon sources, i. e
4 .研究了無機鹽和碳氮源對青黴pt95菌株菌核生物量和類胡蘿卜素產率的影響作用，結果表明:供試的4種無機鹽中， kzhpo ;的單因子效應最好; kzhpo4 + kci + mgs04表現出最好的正協同效應。 -
The positive colonies that grew on the ampicillin ( amp ) plate ( lb agar medium contaning 100 g / ml amp ) were screened and identified. sds - page and western blot analysis were performed to study the expression profiles of target gene cein in e. coli
從轉化的平板中篩選出陽性重組子，進行不同iptg濃度和不同誘導時間的表達研究，並利用sds - page電泳和westernblotting蛋白質印跡技術對外源基因cei _ （ 12 ）在大腸桿菌e -
After linerization, the recombinant plasmid was transformed into pic hia pastoris by electroporation, which then were cultured in md plate free of histidine, from which the positive colones were propagated
重組質粒線性化后，用電擊法將重組質粒轉化入巴氏畢赤酵母，在缺組氨酸的md板上篩選陽性菌落，然後用不同濃度的g418 ? ypd板篩選多拷貝插入單菌落。 -
At first, 1. 67 u g per well mcab all was coated on three wells of a plate, and then 1. 5 x 1011 phage virion was diluted and added, after incubating with the target, wash away unbound phage by tbst ( 0. 1 % tween - 20 ), the bound phage was eluted with ph 2. 2 tris - gly buffer and amplified, the specially bound phage was enriched by taking through addition binding / amplification cycles. ln the following cycles, the stringency of panning can be increased by raising the concentration of tbst or decreasing that of mcab all, collecting and titering the washing phage of last time and output phage in each round, the selective ratio and the false positive rate of each round were worked out, the gradually increasing of selective ratio and decreasing of positive rate shows that the panning was effective. after 4 rounds of panning, 11 phage clones were selected after competitive - ellsa, the dna samples of 8 positive clones and 1 negative clone were sequenced and all the foreign peptides inserted was also deduced, a clear consensus binding sequence emerged
在本實驗中，利用隨機12肽庫對抗豬瘟病毒（ classicalswinefeverviruscsfv ）糖蛋白me2的單抗a11進行表位篩選，經過四輪篩選以後，隨機挑取11個克隆作競爭- elisa檢測，結果表明，所挑11個克隆中，有9個克隆能對me2蛋白和a11反應產生抑制作用，抑制率最高可達64 ； dna測序以後經過dnastar軟體分析，發現它們的核心序列為anwralsl ，該核心序列與豬瘟病毒e2蛋白的28 - 35位氨基酸ttwkeysh具有同源性；夾心- elisa檢測和western - blotting試驗均證明所挑陽性克隆能被a11所識別；人工合成含核心序列的多肽經間接elisa試驗證實，也能被a11識別。 -
Then the linked products were transformed into the high competent cell of e. coli dh5a. based on - complementation of the detective - galactosidase, positive recombinant clone were screened from x - gal plate
從引物和基因序列的比對分析結果看， zhyf006序列與上下游引物的配對比例分別為s4 -
Lead storage batteries ; stationary cells with positive plante plates, narrow plate distance ; rated capacities, main dimensions
鉛酸蓄電池.帶有大型正極板的窄板距固定式畜電池.公 -
And it is well known that the non - uniform current and potential distributions on the plate can obviously affect the active mass utilization, especially for the positive plate
而且極板上不均勻的電流和電位分佈會明顯影響活性物質的利用率，尤其是正極板。 -
When it is discharged at high - rate, the distributions are also the most uniform at the end of the discharge. this indicates that the positive plate with the red lead has the better discharge performance than the other two kinds of positive plates
含紅丹的正極板在化成初期電流密度和電位的分佈最均勻，極化最小，在高倍率放電結束時，其電流密度和電位分佈也最均勻，表明含紅丹的正極板的放電性能比其它兩種正極板好。 -
During the formation, the positive plates with red lead and bapbo3 additives are easier formed than that without additive, so the current and potential distributions on the plates with additives are more uniform than that without additives in the early stage of the formation. these distributions on the plate with red lead are the most uniform, and the polarization is the smallest
在正極板化成過程中，含紅丹和鉛酸鋇鉛膏的正極板比不含添加劑的正極板更容易化成，所以在化成初期含添加劑正極板的電流密度和電位分佈比不含添加劑正極板上的電流密度和電位分佈更均勻。 -
Amplified in e. coli xi - blue, the eluted phage in the third rounds was poured onto lb / iptg / xgal plate. we selected randomly 18 clones and amplified them, then confirmed positive clones by elisa
經雙抗體（流感病毒的多抗和辣根過氧化物酶標記m13噬菌體抗體）夾心elisa鑒定的陽性克隆有12個，分別將其純化、並進行dna序列分析。 -
The apparent density of reticulated positive current collectors and parameter of the plate were decreased, and the utilization efficiency of pam and the cycle life of the batteries were improved
鍍鉛泡沫碳化矽集流體明顯降低了集流體的表觀密度和陽極板的參數，顯著提高了活性物質的利用率，延長了電池的循環壽命。 -
The assay system of the biological activity of lymphotoxin was established using l929 cell as the sensitive target, lt international standard as the positive control and crystal violet staining method to detect viable cell after treated with lt. the best relationship between dosage and effect could be got if the cell seeding density in cell plate was 1. 6 0. 1 104 the dosage of amd was lug / ml, and the starting concentration of dilution in the plate of lt standard was 10 iu / ml with two fold dilution. the credibility of the established system was detected with rhtnfp developed by r & d
為確定經上述步驟純化后得到的目的蛋自lt 27的生物活性，本研究以l929細胞為靶細胞、淋巴毒素國際標準品為參照，採用結晶紫染色法檢測經淋巴毒素處理后存活的細胞，對淋巴毒素生物活性測定的細胞接種濃度、淋巴毒素標準品板上稀釋的起始濃度和梯度稀釋的倍數、放線菌素d的使用劑量等進行條件實驗后，建立了人淋巴毒素生物活性測定方法。 -
Based on the analysis about the test requirements and the saturated magnetization of the armor plate, the excitation magnetic circuit satisfying the testing condition and a validation system are designed. because the geometric, of the magnetic leakage at the direction of the normal of the roundness fault has the feature of two peaks : a positive and a negative, using the linear regression and the software matlab, two regression equation are proposed : one is about the peak value of the magnetic leakage and the diameter and depth of the roundness fault ; the other is the distance between the two peaks and the diameter of the roundness fault. the result of the validation system proves that the two equations are valid, and an applied method using for quantificationally inspecting the roundness faults is proposed according to the two equations
根據實驗要求，通過對鋼板達到飽和磁化的必要性進行的分析，設計了符合試驗條件的勵磁磁路，並設計了一套實驗驗證系統；根據圓形缺陷法線分量漏磁場幾何圖形正負雙峰值的特點，採用線性回歸擬合的原理和matlab軟體及其統計工具箱中的相關函數，給出了圓形缺陷漏磁場幾何圖形的峰峰值與圓形缺陷的直徑和深度以及峰峰值間距與圓形缺陷直徑的兩個回歸擬合方程，並通過實驗驗證系統驗證了擬合方程的正確性，利用這兩個簡單實用的擬合方程，提出了一種工程定量檢測圓形缺陷的應用方案。 -
The interesting gene fragment with ecori and noti were amplified by overlapping pcr, which inserted into vector plasmid ppic9k after degisted by ecori and noti, and the recombinant plasmid was transformed into competent dh5cc. positive clones were screened by pcr from the lb plate with amp. digesting analysis resulte shows that the interesting gene were inserted into the vector ppic9k with correct direction
目的基因經雙酶切后連接載體ppic9k ，然後導入大腸桿菌dh5中，在含氨卞青霉素（ amp ）的lb板上用pcr反應篩選出陽性菌落，雙酶切結果表明目的基因已插入載體中，且方向正確，測序結果進一步證明人巨細胞病毒重組基因表達質粒成功地克隆了目的基因片段。 -
When the amount of pvdf and acetylene black is 7 ~ 10 % and 8 %, the positive plate obtained possesses optimum properties in our studies
本研究中pvdf粘結劑的添加量在7一10 % ，乙炔黑導電劑的添加量在8 %左右，正極極片的性能最佳。 -
The results give that the positive plate takes on preferable charge - discharge properties only when the amount of additive of pvdf and acetylene black is suitable
結果表明，正極極片中pvdf粘接劑和乙炔黑導電劑的添加量只有適量的時候，正極極片的充放電性能才較好。 -
Lead - acid stationary cells and batteries - specification for the flat positive plate type
鉛-酸固定式電池和蓄電池.平陽極板式電池規范
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