strain cell 中文意思是什麼

strain cell 解釋
應變盒
  • strain : vt 1 用力拉，拉緊，抽緊，扯緊。2 使緊張；盡量使用（肌肉等）。3 強迫，強制；濫用，盡量利用。4 拉傷...
  • cell : n 1 小室，單室；隔間，艙；〈詩〉茅舍；（單個的）蜂窩，蜂房。2 〈詩〉墓穴，墓。3 （大修道院附屬的...
  1. The result showed that this strain have a strong ability to decompose the filter paper cellulose. in the process of degrading fibre, the strain adhere tightly to the fibre through its bacilliform cell

    結果表明該菌具有較強的分解纖維素的能力，菌株在降解纖維素濾紙過程中與纖維素物質緊密結合，同時菌體嵌入到濾紙纖維內部。
  2. The bacteri of strain tl2 were found to be mainly distributed in the intercellular space of sclerenchyma in the root, the intercellular space of collenchyma and vascular bundle in the stem, the stomatal apparatus, the intercellular space of epidermal cell, collenchyma and endodermis in the leaf

    其菌體主要分佈在根部厚壁組織的細胞間隙，莖部厚角組織的細胞間隙、維管束等組織的細胞間隙、葉片的氣孔器附近、上下表皮細胞間隙、厚角組織細胞間隙以及內皮層組織細胞間隙等。
  3. Magical fire ( eye doctor ) looks at well - being cream of sticking drawing tradition traditional chinese medicine formula famous and precious in tsinghua, is tied in wedlock modern up - to - date medicine result of scientific research, the various chinese medicinal crop famous and precious being carefully chosen, adopt the modern nano - technology and target to poison a technology to being given to, let various active material, tiny molecule, nutrition factor glutathione etc. guide medicine it is all right for to go ahead, the brute force passes through blood eye parclose, make pesticide effect reach nidus directly location, prompt the nutrition replenishing an eye with the part ( include ciliary muscle, retina, crystalline lens, optic nerve ), active eye part cell, improve eye part immunocompetence and oxidation resistance, boost an eye part organizing an assimilation of the new and excretion of the old, microcirculation improving and restoring an eye part, thereby reach eliminate look at strain, purpose improving and improving sight

    清華神火視康貼汲取傳統中藥名貴配方之精華，結合現代醫藥最新科研成果，精選多種名貴中藥材，採用現代納米技術和靶向給藥技術，讓多種活性物質、微分子、營養因子谷胱甘肽等引藥上行，強力穿透血眼屏障，使藥效直達病灶部位，迅速補充眼部（包括睫狀肌、視網膜、晶狀體、視神經）的營養，激活眼部細胞，提高眼部免疫能力和抗氧化能力，促進眼部組織新陳代謝，改善和恢復眼部微循環，從而達到消除視疲勞，改善和提高視力的目的。
  4. Initial talking about the temperature compensation of strain gange load cell

    應變片式傳感器的溫度補償淺談
  5. A pair of primers were chemically synthesized based on the cdna sequence of hog cholera virus strain brescia and used to amplify the cdna fragments of envelope glycoprotein e2 gene of hclv which coding the major protective antigen by reverse transcription - polymerase chain reaction ( rt - pcr ) from total intact rna extracted from infected calf testicle cell culture by hclv

    以豬瘟兔化弱毒犢牛睪丸細胞毒（ hclv ）中提取的細胞總rna為模板，以rt - pcr技術，擴增出了完整e2基因的cdna片段。經電泳、酶切分析，證實了所擴增片段為e2基因特異性片段。
  6. This research is a part work of the " 863 " international project - " the technique of producing l - methionine by gene - engineering strain of immobilization cell "

    本項研究是國家「 863 」中試項目「工程菌固定化細胞生產l ?蛋氨酸技術」的部分基礎研究工作。
  7. The e. coli strain jm109 was transformed with resultant plasmid pgex - 4t - 1 / 6 - 4. 4. the transformation was induced with iptg, then the total protein from cell extract was analyzed by electrophoresis on a 8 % sds - page in order to validate the gst fusion protein, and the fusion protein is about 90kd

    4 .用工ptg誘導含pgex一4t一1 / 6一4的轉化菌，提取初提物中的總蛋白，進行sds一聚丙烯酞胺凝膠電泳，檢測表達的融合蛋白大小越為gokd 。
  8. 4. engineering dhqase ( arod ) - deficient e. coli mutant with a second copy of the arob gene gene targeting technique was used to disrupt the arod gene in e. coli chromosome. the mutant 31bk was engineered, in which homologous recombination of the arobkanr gene cassette into the arod locus ( arod : : arobkanr ) of the e. coli strain atcc31884 genome utilized the helper plasmid pkd46 with red system. the host cell 31bk lacked catalytic activity of dhqase ( arod ) and had a second copy of the arob gene, so it improved carbon flow into the quinic acid biosynthesis direction

    構建宿主菌基因精確定位突變株31bk （ arod : : arobkan ~ r ）為了改變代謝途徑脫氫奎尼酸（ dhq ）分支點上的代謝流量，使之充分流向目的產物奎尼酸合成方向，利用基因打靶技術構建了31884宿主菌arod基因精確定位插入突變體，使dhq脫水酶（ dhqase ）失活，阻斷了碳代謝流流向芳香氨基酸生成的方向，同時用同源重組的方法將arob基因定位整合入染色體上，解除了限速酶對碳代謝流通過共同途徑到達dhq的阻遏影響，並減輕代謝負擔。
  9. Halocin c8 appeared to have a very wide activity spectrum, including most haloarchaea and even some haloalkaliphilic rods, but it showed no inhibitory activity against bacterial strains tested. when a sensitive strain of halorubrum saccharovorum atcc29252 was exposed to halocin c8, the treated cells swelled at the initial stage, the cell wall appeared to be nicked and the cytoplasm was extruded out afterwards, and the whole cell was eventually completely lysed

    將敏感菌株halorubrumsaccharovorumatcc29252的細胞用嗜鹽菌素c8處理后，採用電鏡觀察，發現處理2小時后細胞開始腫脹、膨大，接著在細胞的兩端出現裂口，細胞內容物開始向外溢出，隨著時間延長，裂口越來越大，發生這種變形的細胞也越來越多，最後，幾乎所有的細胞完全裂解。
  10. In this stlidy, g5 serotype a gidup poreine rotavha stanha strain osu was propagated on ma - l04 monolayer cell

    本研究用恆河猴胚腎細胞（ ma - 104細胞系）繁殖並擴增了a群prvg5型標準毒株osu 。
  11. Instead of using an adhesive bond strain gauge, laser spots are used to achieve an atomic bond between the deformation body and measuring cell

    使用激光點焊代替膠結技術應變測量儀來實現變形體和測量元件的原子連接。
  12. From dead chicken which infected infectious stunting syndrom of our province, one virue was isolated using spfeggs, chicken embryo fibroblast, mdck18, and vero cell. this virus was unable to agglutinate chicken erythrocytes. in order to definite the pathogeny of infectious stunting syndrom. physical and chemical specific property, types of the nucleic acid of the isolated virus, recurrent infection and other biological property determination and indirect elisa test proved it as a parvoviruses like strain of chicken

    為確定該病的病原，對所分離病毒進行了理化特性測定、病毒核酸型別測定、動物回歸試驗等生物學特性測定，證明該分離病毒與細小病毒科（ parvovirdae ）細小病毒屬（ parvovirus ）的雞細小病毒（ chickenparvovirus ）特性基本相符，核酸型為dna型。
  13. Es cell line ; c57bl 6j strain ; conditioned media of rat myocardial cells ; chimera ; immortalization

    Es細胞系c57bl 6j小鼠品系大鼠心肌條件培養基嵌合鼠永生化
  14. Technology and key craft of high - temperature strain gauge load cell

    高溫應變式稱重傳感器技術與關鍵工藝
  15. Technology and key craft of high - temperature strain gauge load cell receive last issue

    高溫應變式稱重傳感器技術與關鍵工藝接上期
  16. The hwtx - i gene was chemically synthesized according to its known cdna sequence, the gene was inserted into vector ppic9k which contained aoxj promotor and the sequence of a secreting signal peptide - a - factor, the cloning ppic9k / hwtx - i was constructed and confirmed by two - step pcr and dna sequence analysis, then it was transformed into host strain gs115, a his + muts cell line was screened and multicopy transformants were screened by various g418 concentrations, the multicopy transformant was named gh1. gh1 was cultivated in flasks. after 6 days of induction by 0. 5 % methanol, the supernatant was checked by 16. 5 % tricine - sds page, which showed there was a band in the position of 3. 5 - 6. 1kd, then it was isolated and desalted by ultrofiltration followed by ion exchange of cm column, after reverse phase hplc of ci8 and vacuum drying, the purified rhwtx - 1 was obtained which was proved to be correct recombinant hwtx - i by tricine sds - page, maldi - tof mass spectrometry, amino acid composition analysis, the n - terminal amino acid sequence and its biological activity, the final field of the purified rhwtx - i was about 80mg / l, accounting for 23. 6 % of it total secretory proteins

    將帶有hwtx -基因的ppic9k經blgii線性化后，轉化酵母宿主菌gs115原生質體后經篩選陽性克隆並經表型鑒定為his ~ + mut ~ s酵母菌，進一步用遺傳毒素g418篩選多拷貝的轉化菌株，命名為gh1 ；將gh1甲醇酵母菌用0 . 5的甲醇誘導表達，發酵上清經90飽和度的（ nh _ 4 ） _ 2so _ 4沉澱， yw - 3 （ mwc03000 ）的超濾膜超濾，再經cm陽離子交換， c _ （ 18 ）反相hplc純化得到分子量為4kd左右的組分，其中4289 . 05的組分經質譜鑒定，氨基酸組成分析和序列測定為正確的表達產物，生物學活性表明其活性為天然毒素活性70 % ，表達量為80mg / l 。
  17. Methods serums containing whole wmt and its disassembled formulas, including the formula consisted of warming jing and boosting qi part wenjin yiqi, wy and that of promoting blood circulation part huoxue tongmai, ht, as well as the serum contained high concentration of lipids were prepared conventionally, respectively. the adhesion of monocytes cell strain thp1 to human umbilical vascular endothelial cells huvec was determined by rose bengal stain method, and elisa was used to detect expressions of intercellular adhesion molecule icam1, vascular cellular adhesion molecule vcam1 and p selectin on huvec surface

    方法常規制備溫脈通全方溫經益氣拆方活血通脈拆方含藥血清和高脂血清，採用虎紅染色法檢測藥物血清對高脂誘導的人臍靜脈內皮細胞huvec和單核細胞株thp1黏附的作用用細胞elisa法檢測huvec表面細胞間黏附分子1 icam1血管細胞黏附分子1 vcam1 p選擇素pselectin的表達。
  18. So some methods suitable to large plasmid extraction, including lysis by sds and a method from a literature, were used to try to extract the large plasmid from the strain cell. the lysis reactions in these two methods are gentle, so the large plasmid cannot be injured in the lysis process, opposite to lysis by alkali. it would be helpful to keep the integrality of the large plasmid during the extraction

    因此我們採用了適合於大質粒提取的sds法，和文獻中應用於硝基苯降解性質粒的提取方法，來嘗試對菌株細胞進行質粒提取，這兩種方法裂解反應溫和，不會像堿裂解法那樣，在裂解過程中損壞質粒，可以實現質粒提取的完整性。
  19. To determine the plasmid function, the experiment is done to cure the plasmid from the cell, which will cause some change on the strain physiology. the result show that after curing the plasmid, the strain cell cannot grow on the selective medium containing nitrobenzene

    為了考察質粒的功能，進行了質粒消除實驗，結果表明，質粒消除后的菌株細胞難以在硝基苯選擇培養基上生長，表明這個質粒是與硝基苯的降解代謝過程有關的。
  20. Then the strain cell is detected to determine weather there is any plasmid in the cell. the detection result analysed by gelose gel electrophoresis shows that the cell harbors a plasmid, and this plasmid is relatively large

    應用質粒檢測的方法，對菌株細胞進行質粒檢測，並對檢測結果進行電泳分析，實驗發現，菌體細胞中存在一個質粒，而且質粒較大。
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