插入移位 的英文怎麼說

中文拼音 [chārùyíwèi]
插入移位 英文
insertional translocation
  • 插 : 動詞1. （把細長或薄的東西放進、擠入、刺進或穿入; 插上; 插進） stick in; insert 2. （中間加進去; 加進中間去） interpose; insert
  • 入 : Ⅰ動詞1 （進來或進去） enter 2 （參加） join; be admitted into; become a member of 3 （合乎） conf...
  • 移 : Ⅰ動詞1. （移動） move; remove; shift 2. （改變; 變動） change; alter Ⅱ名詞（姓氏） a surname
  • 位 : Ⅰ名詞1 （所在或所佔的地方） place; location 2 （職位; 地位） position; post; status 3 （特指皇帝...
  • 插入 : insert; infix; run in; break in; patch; insertion; plug in; intercalate; intercalation; intromiss...
  • 移位 : bit shift
  1. The recombinant transfer vector pbacpak - hbmp was constructed by insertion of the hbmp coding sequences into the multiple cloning site of transfer vector pbacpak. 8. bmn cell line was co - transfected with pbacpak - hbmp plasmid and linearized baculovirus bacpak6 dna by dosper agent

    將克隆到的hbmp基因通過適當的酶切插入到轉移載體質粒pbac - pak8的多克隆位點中，獲得重組轉移載體質粒pbacpak - hbmp 。
  2. In addition, the test results also demonstrate that bond - slip response between angle steel and concrete foundation in tension could be reflected with the displacements between angle steel and concrete, because bond stress is obviously decreasing with the cross section shrinking, that is effects of poisson ' s ratio

    另外，試驗結果還表明：在一定的拉應力下，插入角鋼與混凝土之間的粘著力能通過插入角鋼與混凝土之間的位移反映出來。這是由於橫斷面的收縮，使得粘著應力明顯降低，即泊松比效應。
  3. Button to move the insertion point to previous locations in the active document, and the navigate forward button to return to more recent locations

    使用「向後定位」按鈕可將插入點移動到活動文檔中前面的位置，而「向前定位」按鈕則返回到更近的位置。
  4. According to the guidline, two nd : yag lasers have been designed and set up, one is end - pumped by lower output power ld using a selfoc micro lens, and the other is end - pumped by high output power ld using a pair of lenses are designed, and the characteristics such as output power and power stabilization of both solid - state lasers are investigated. thirdly, when an empty liquid crystal cell is inserted in the cavity of the nd : yag laser pumped by high power ld, the laser can operates in single axial mode. finally, according to the relationship between the laser output power and the longnitudinal a ld - end - pumped nd : yag laser sensor for displacement measurement has been investigated theoretically and demonstrated experimently, the results indicate that when the mean radius of pumping inside the laser cavity is far less than that of the oscilating laser mode, the exponential of the output power is a gauss function of the longitudinal positon of focused spot of ld pumping beam, both the measurement range and the sensitivity are dependent on the incident pumping power, as the incident pumping power is increased, the measurement range is enlarged and the sensitivity is improve d

    本文首先介紹了ld泵浦nd ： yag激光器的發展狀況、主要特性及其應用，從四能級速率方程出發，推導了ld泵浦nd ： yag激光器的閾值、輸出功率和斜效率的表達式，並簡述了激光器的工作原理、結構型式和倍頻方法；其次，以空間相關的速率方程為基礎，提出了ld端面泵浦nd ： yag激光器的設計方法，給出了一定泵浦耦合方式下，振蕩光模尺寸、最佳輸出耦合率、泵浦光模尺寸、泵浦光焦斑位置等參數的選取依據，以此為依據，設計了自聚焦透鏡耦合小功率ld泵浦nd ： yag激光器和透鏡組耦合高功率ld泵浦nd ： yag激光器，對激光器的輸出功率和功率穩定性等特性進行了實驗研究；再次，在帶尾纖輸出的高功率ld泵浦nd ： yag激光腔內插入一隻空液晶盒，觀察到了激光器以單縱模運轉；最後，根據泵浦光焦斑端面位置對激光輸出功率的影響規律，提出了ld端面泵浦nd ： yag激光位移傳感新方法，並進行了理論和實驗研究，研究結果表明：當激光晶體內泵浦光平均光斑半徑遠小於振西安理工大學碩士學位論文蕩光束腰半徑時，激光輸出功率的自然指數與泵浦光焦斑的縱向位置成高斯變化規律，測量范圍和靈敏度依賴于泵浦功率，隨著泵浦功率的增加，測量范圍擴大，靈敏度提高，當端面泵浦功率為7 . 24w （最大輸出功率為1 . 926w ）時，激光位移傳感器的測量范圍和靈敏度分別是13 . 045mm和0 . 148mw / pm 。
  5. In explanation, if inserting a character would cause a character to be shifted over into a mask position where it would not be valid, the character insertion will be rejected

    將拒絕用戶輸入的字元。具體地說，如果插入一個字元會導致某個字元移至使其無效的掩碼位置，將拒絕插入該字元。
  6. The user is trying to input extraneous characters beyond the end of the mask either because the mask has already been filled or the current caret position has been moved to the very end of the displayed input mask string

    用戶試圖在掩碼末尾的後面輸入無關字元，這可能因為掩碼已填充完畢，或者當前插入字元的位置已移至顯示的輸入掩碼字元串的最末端。
  7. In the code editor, move your mouse pointer where you want to insert code. on the tools

    在代碼編輯器中，將鼠標指針移動至要插入代碼的位置。
  8. Inserts a zero bit in the lowest position on each shift

    在每一移位的最低位置插入零位。
  9. Inserts a zero bit in the highest position on each shift

    Shr . un在每一移位的最高位置插入零位。
  10. Based on a 3. 1kb pst i fragment of genomic dna of a wild s. avermitilis, a 1. 5 kb apramycin resistance fragment was inserted into sph i site of avec gene in the 3. 1 kb fragment, then a recombinant plasmid pc05 was obtained by introducing above inactivated avec fragment into mcs region of phjl401. competent cells of et12567 were transformed by recombinant plasmid pid03 and pc05 respectively

    以含有avec基因的3 . 1kb基因組dnapsti片段為基礎，將1 . 5kb的安普黴素抗性基因片段插入到avec基因中的sphi酶切位點，再將此插入失活的avec基因片段連接到具有接合轉移功能（含有orit基因）的鏈黴菌-大腸桿菌穿梭質粒phjl401的多克隆位點區，由此得到重組質粒pc05 。
  11. Finally, it takes a detailed test to the processed millimeter 4 - bit digital phase shifter. the test result is better than expectant guideline : the maximum of the phase error is 10, the insertion loss is better than 10. 74db, the return loss is more than - 14. 88db in the 33. 9ghz 34. 5ghz frequency band. the whole volume of the phase shifter is 80mm 35mm 20mm

    最後，對加工出的毫米波四位數字移相器進行了測試，測試結果完全達到了預定指標要求:在所要求的33 . 9ghz 34 . 5ghz頻帶內，最大相移誤差小於10 ，插入損耗小於10 . 74db ，輸入輸出回波損耗大於- 14 . 88db ，整個電路尺寸為80mm 35mm 20mm 。
  12. To reposition a group within the collection, you must first remove it, and then insert it at the desired index

    若要在集合中對組進行重新定位，必須先將該組移除，然後再插入所需索引處。
  13. A 1. 5 kb apramycin resistance fragment was inserted into nru i site of aved gene and the inactivated aved gene fragment was then introduced into mcs region of phjl401 - an e. coli / streptomyces shuttle vector with conjugation function ( containing orit gene ). as a result of above procedures, a recombinant plasmid pid03 was obtained

    將1 . 5kb的安普黴素抗性基因片段插入到aved基因中的nrui酶切位點，再將此滅活的aved基因片段插入到具有接合轉移功能（含有orit基因）的鏈黴菌?大腸桿菌穿梭質粒phjl401的多克隆位點區，由此得到重組質粒pid03 。
  14. A new e. coli promoter - probe vector phn1005 was constructed by using a red - shift enhanced gfpmut3 as reporter gene and showed the following characters : 1, bamhi at the 5 " end of gfpmut3 structure gene could be used to clone promoter - active fragment and the strength of promoter could be quantitatively assayed. 2, a rrnbtlt2 terminator from rrna gene at the 3 " end of gfpmut3 could permit clone strong promoter. 3, another rrnbt1t2 terminator was inserted upstream bamhi to prevent reading through of promoters from puc19

    進一步以紅移且熒光強度提高21倍的gfpmut3為報告基因，構建了大腸桿菌啟動子探針載體phn1005 ，該載體上gfpmut3結構基因5 』端的bamhi位點可用來克隆具有啟動子活性的dna片段並定量分析插入的啟動子強度；其3 』端含rrnat1t2終止子，可允許克隆強啟動子；在bamhi上游同樣插入rrnat1t2終止子以防止載體puc19上的啟動子的轉錄通讀； gfpmut3結構基因上游還插入一段內含子序列使正反六種讀碼框的翻譯均可被終止，可保證gfpmut3以正確的讀碼框翻譯。
  15. The dcb ( double cantilever beam ) met hod to test the interlaminar toughness of fabric - reinforced laminates and the modified compliance calibration method ( mcc ) were adopted in this research. the double cantilever beam ( dcb ) test was executed for stitched laminates to evaluate the interlaminar fracture toughness. the stitch parameters ( stitch line spacing and pitch spacing ) were changed and their effects on interlaminar fracture toughness were examined by means of dcb test by using improved insert type loading fixture

    試驗中採用改進的插入型夾具、雙懸臂梁dcb （ doublecantileverbeam ）試驗方法，測試了載荷?試樣開口位移曲線，依據改進的柔度梁方法（ modifiedcompliancecalibrationmethod （ mcc ） ）計算出了各個試樣的層間斷裂韌性（ r曲線）及層間斷裂韌性的平均值，闡明了縫合工藝參數與層間斷裂韌性（ g _ （ ic ） ）間的關系，以拉伸與彎曲強度為約束條件，以層間斷裂韌性值為目標優化了縫合工藝。
  16. When selected, pressing the esc key undoes the selection and moves the insertion point in the editor to the position where the current selection began

    選定后，按esc鍵將撤消選擇並將編輯器中的插入點移到當前選擇開始的位置。
  17. In dom level 2, renaming and moving nodes from one document to another can be relatively expensive, since these operations involve creating new nodes, copying the contents of those nodes, and inserting nodes at the appropriate places in a tree

    在dom level 2中，重命名節點和將節點從一個文檔移到另一個文檔的代價可能相當高，因為這些操作需要創建新節點，復制那些節點的內容，並將節點插入到樹中適當的位置。
  18. Property is true, the input will overtype the prompt character and insertion point will be moved to the next position in the mask

    屬性為true ，輸入將覆蓋提示字元，插入點將移至掩碼中的下一個位置。
  19. In this study, a 1. 7kb kpni fragment and a lacz gene expression cassette carrying the e. coli lacz gene under the control of sv40 promoter were inserted into the transfer vector pbdtk - uni ( a 277bp acci - accl fragment in the tk gene was deleted ). the new transfer vector was called puni - lacz. the transfer vector puni - lacz and purified genomic dna of strain bartha - k61 were used to cotransfect vero cells using lipofectin transfection procedure

    本研究以呈ge ~ -表型的經典弱毒疫苗bartha - k61株為親本株，在通用prv轉移載體pbdtk - uni的基礎上，在其多克隆位點中插入由sv40早期啟動子控制下的lacz基因表達盒，同時將下游同源臂增加了一個1 . 7kb的kpni片段，使上下游同源臂的長度都超過了1kb ，構建了一個新的轉移載體puni - lacz 。
  20. The gd and ge gene was subcloned into puc18, resulting in pugdge. the fragment from pcdnas. 1 - including hcmv promoter / enhancer, mcs and neomycin resistance gene was inserted into the bamhi and bsteii restrication sites of pugdge, resulting in the universal transfer vector pgd - m - ge. the universal transfer vector pgd - m - ge has deleted the gi gene and 363bp in the 5 ' end of the ge orf of prv. there were 11 restrication sites for insertion of the foreign gene. the upstream and downstream flanking sequences were up to 1. 25kb and 1. 42kb. it will be useful for developing the recombinant prv expressing foreign gene ( s )

    將gd 、 ge基因連接于質粒puc18獲得pugdge ，缺失質粒pugdge的bamh和bste位點間391bp的片段。在此缺失位置插入來自質粒pcdna3 . 1 -的一偽狂犬病病毒gd 、 ge 、 tk基因的克隆與通用轉移載體的構建段含hcmv啟動子。多克隆位點和neo報告基因的片段，構建了通用轉移載體ppd m pe 。
分享友人
分享到 Line

分享到臉書