載重量表 的英文怎麼說

中文拼音 [zǎizhòngliángbiǎo]
載重量表 英文
dead weight scale
  • : 載Ⅰ名詞(年) year : 一年半載 six to twelve months; six months to a year; 三年五載 three to five ...
  • : 重Ⅰ名詞(重量; 分量) weight Ⅱ動詞(重視) lay [place put] stress on; place value upon; attach im...
  • : 量動1. (度量) measure 2. (估量) estimate; size up
  • : Ⅰ名詞1 (外面;外表) outside; surface; external 2 (中表親戚) the relationship between the child...
  • 載重 : load; carrying capacity
  • 量表 : scale量表程序 scalogram
  1. The physicochemical properties of cx - 2 correspond to cytodex - 3 mc produced by pharmacia, including of color, loss of drying, area, density, size, soakage, dilation, stability, size distribution, mechanical strength, surface structure, etc., but its cost of manufacture is lower than cytodex - 3 " s

    通過優化工藝制備的cx - 2微體,在色澤、乾燥失、比面積、成球率、密度、直徑、吸水、溶脹度、粒度分佈、面結構、機械強度、穩定性等理化指標與pharmacia公司cytodex - 3微體相當,但成本價格要低得多。
  2. By the check - out, inspection and measurement to start construction the industrial art to this test pile with the examination between stake body mass and bearing power, made sure the stroke reasonable operation method drilling under the dissolved cavern geology term ; the pier foundation loading test expressed the lading and rub the lading that resistance drag a glazing for of relation, and to the borehole cast - in - place concrete pile in the karst terrain deliver with break the mechanism, the characteristic of bearing power, proceeding the spot test job of the full of result ; the test data expresses the stake side friction resistance to rises with a bat batch terminal friction resistance very important function, the of tip of pile resistance drag occupies the proportion very few

    通過對本次試樁施工工藝的檢測和樁身質及承力的檢驗,確定了沖擊鉆在溶洞地質條件下的合理使用方法;基樁承實驗明了荷與摩擦阻力之間的關系,並對巖溶地區的嵌巖灌注樁的荷傳遞和破壞機理、承力特性,進行了富有成果的現場測試工作;試驗數據明樁側摩阻和支盤端阻起很要的作用,樁端阻力所佔比例甚少。這與設計樁基時的計算模式相差很大,承力也較設計增加;使用力學數值分析方法和有限單元法,對鉆孔灌注樁樁端下的巖體強度和結構穩定性方面進行模擬計算和定研究。
  3. By recombinant dna techniques, the vp2 gene of gpv hi strain was fused in frame with 6his gene of prokaryotic expression vector pproex - htb. the recombinant expression plasmid of goose parvovirus vp2 gene pproex - htb - vp2 was transformed into e. coli dh5a and induced with iptg. sds - page analysis showed an induced expression product band about 72ku, which correspond to the sizes of vp2, reported in the literature

    利用dna組技術,將其結構蛋白vp2基因亞克隆至原核體pproex - htb , iptg誘導后成功達出與預期大小相符的約72ku的融合蛋白,光密度掃描對達產物進行初步定達產物約占菌體總蛋白的14 。
  4. Honeycomb ceramic has high surface and lighter weight. it is good at the heat insulation, so it is suitable for various kinds of catalyst carriers. it is widely used for automotive emissions control, stationary emissions control, chemical processing and refining industries

    蜂窩陶瓷材料具有比面積大、隔熱性較好及較輕的特點,因此它適用於各種用途的催化劑體,現已被廣泛應用於汽車尾氣凈化、固定氣體排放的凈化、化學工藝、精練工業等方面。
  5. Banks assume no liability or responsibility for the form, sufficiency, accuracy, genuineness, falsification or legal effect of any document, or for the general and or particular conditions stipulated in the document or superimposed thereon ; nor do they assume any liability or responsibility for the description, quantity, weight, quality, condition, packing, delivery, value or existence of the goods represented by any document, or for the good faith or acts and or omissions, solvency, performance or standing of the consignors, the carriers, the forwarders, the consignees or the insurers of the goods, or any other person whomsoever. article 14 - disclaimer on delays, loss in transit and translation

    銀行對任何單據的格式完整性準確性真實性虛假性或其法律效力或對在單據中明或在其上附加的一般性及或特殊性的條款,概不承擔責任或對其負責銀行也不對任何單據所示的貨物的描述數狀況包裝交貨價值或存在或對貨物的發運人承運人運輸代理收貨人或保險人或其他任何人的誠信或作為及或不作為清償力業績或信譽承擔責任或對其負責。
  6. Banks assume no liability or responsibility of the form, sufficiency, accuracy, genuineness, falsification or legal effect of any document ( s ) or superimposed thereon ; nor do they assume any liability, condition, packing, delivery, value of existence of the goods represented by any document ( s ), or for the good faith or acts and / or omission, solvency, performance or standing of the consignors, the carriers, the forwarders, the consignees or the insurers of the goods, or any other person whomsoever

    銀行對任何單據的格式、完整性、準確性、真實性、虛假性或其法律效力、或對在單據中明或在其上附加的一般性和/或特殊性的條款不承擔責任或對其負責;銀行也不對任何單據所示的貨物的描述、數、質、狀況、包裝、交貨、價值或存在、或對貨物的發運人、承運人、運輸行、收貨人和保險人或其他任何人的誠信或行為和/或疏忽、清償力、業績或信譽承擔責任或對其負責。
  7. In this study, we designed a pair of primers based on the sequence of the upstream and downstream of chicken il - 2 gene. about 600 bp chicken il - 2 cdna fragment was cloned from cona - stimulated chicken splenocytes by reverse transcription - polymerase chain reaction ( rt - pcr ) and was subcloned into puc18 vector. recombinant clone was demonstrated by restriction enzyme digestion and dna sequencing. next, we construct recombinant plasmid pproex ? t - il - 2. the cdna of chicken il - 2 gene was subcloned into bamh i / hind iii sites of vector. the recombinant plasmid pproex ? t - il - 2 was transformed into e. coli dh5a and the bacteria was induced with iptg. it was demonstrated by sds - page and western blot that a 18kda protein which was equal to chicken il - 2 protein in molecular weight was expressed in e. coli dh5a. the expression level was up to 30 % of the total bacterial proteins. the purified protein was used to prepare the antibody against chicken il - 2 protein

    經酶切鑒定及dna序列測定,該基因為雞il - 2基因,其序列與sundick等報道的完全一致。在此基礎上,我們把雞il - 2基因亞克隆到大腸桿菌原核體pproex ~ ( tm ) ht中,構建達質粒並進行確證性序列測定,組質粒測序結果明將編碼雞il - 2成熟蛋白的基因正確地插入到原核體pproex ~ ( tm ) ht的目的位點。組質粒轉化受體菌dh5後用iptg於37進行誘導培養, sds - page和westernblot分析顯示,達的雞il - 2融合蛋白分子約為18kda ,達的融合蛋白經薄層掃描發現目的蛋白約占菌體蛋白的30 。
  8. This method has three merits : first, reduce the harm to the battery ; second, this current is stable ; the last, the current may represent the battery ' s current function better. in order to study this problem, we design a install to make lots of experiments to prove this result. the install can use in the factory as a automation instrument if it be perfected

    此方法和原有方法比較有三大憂點:一是減少了直接短路時大電流放電對電池的損傷:二是此迴路電流值穩定存在,可以對其進行比較準確的測:三是此電流值更能代堿錳電池實際工作時的放電性能c為了本研究的順利實施,本課題提出了一個堿錳電池四參數檢測的實驗平臺,做到對電池的開路電壓、負電壓、電流指標、電池四參數的檢測。
  9. The test results demonstrate that this prototype has excellent comprehensive performances such as small bulk, lower weight, high efficiency, high steady precision, fast dynamic response, wide range input voltage, good output waveforms, strong over - load and short - circuit ability, and strong function with different nature load and three - phase unbalanced load

    試驗結果明,該變流器具有體積小、變換效率高、靜態精度高、動態響應快、輸入電壓變化范圍寬、輸出波形質高、過與短路能力強、帶不同性質負和帶三相不平衡負的能力強等優良的綜合性能。
  10. 6 hours later, the amount of the expression yield of cp accounting for the total protein of the cells was 28. 9 % ( about 2mg / ml cp ). after sds - page, the recovery of cp added the same volume of incomp lete freund adjuvant emulsified completely, injected rabbits by subcutaneous injection. every rabbit was injected 2ml emulsified antigen ( 300ug cp ) once a week

    體導入宿主菌e . colibl21 ( de3 ) ,用終濃度為1mmol / liptg誘導, 37培養6小時后, cp基因的達到最高,每毫升菌液含目的蛋白的約為2mg ; uvi光密度掃描分析明cp基因的占細菌總蛋白的28 . 9 。
  11. These load, speed and mass is reference of choice only

    中所列基本額定荷、極限轉速和,僅供選擇參考用。
  12. Based on the new model, the influences caused by soil structure, apparent preconsolidation pressure, the re - compression index, the coefficient of secondary compression, the magnitude of loading, the coefficient of permeability, the rate of loading, the thickness of clay, the self - weight, the layered property etc, in the process consolidation of soil with structure, are analyzed in detail. the difference between the present model and yin & graham model was also given

    基於本文新建模型,分析論述土結構性、觀前期固結壓力、再壓縮系數、次固結系數、荷大小、滲透系數、加荷速率、固結層厚度、自應力隨深度變化和土體成層性等對土固結的影響,比較本文模型與yin & graham模型的異同,闡述土結構性和流變性對軟土固結壓縮行為的影響。
  13. We integrated dh gene into procaryotic expression vector for the first time, which establish foundation for obtaining dh recombinant protein to research the structure and function of dh

    本研究首次將dh基因整合入原核體中達,為大獲取dh組蛋白,研究dh的結構及功能奠定了基礎。
  14. This paper, regarding the asphalt pavement in the zhoukou region as the study object, according to the prevalent norms ( specifications for design of highway asphalt pavement ), with the beginning of the pavement performance and the transportation investigation, totally and systematically analyzes the traffic parameters and the destroying reason of pavement at the early stage in the point of fatigue property and limit strength, gives the concepts and methods of the growth rate of equivalent axle load action time, seasonal modification factor and overload factor, proposes the method of axle load conversion on the condition of heavy loading. on this basis, it proposes the design method adapting to asphalt pavement construction, explains the steps of thickness computation of construction with the combination of engineering example, finally verifies thedesign method in the paper by test road. theory and practice both prove that the reasonability of pavement structure style and the reliability of design method in the paper can adapt to the present heavy loading and overloading traffic conditions, have highly theoretical and practical value

    本文以周口地區瀝青路面為研究對象,以現行《公路瀝青路面設計規范》為依據,從路面使用性能和交通特徵的調查入手,從疲勞特性和極限強度出發分析了路面早期破損的原因,全面系統地進行了交通參數的分析,提出了當軸次增長率、季節修正系數和超系數的概念和方法,並提出了交通的軸換算方法。在此基礎上,針對超交通從結構組合設計、結構厚度計算(包括疲勞強度標準和極限強度標準)等方面提出了適宜的瀝青路面結構設計方法,並結合工程實測,說明了結構層厚度計算的具體步驟,最後通過試驗路驗證本文提出的設計方法。理論與實踐均明,本文提出的路面結構型式合理、設計方法可靠,能適應目前、超交通的狀況,具有較高理論與實用價值。
  15. The vp6 gene was subcloned from recombinant plasmid pmd18 - t - vp6 into expression plasmid pet - 30a. the recombinant plasmid pet - 30a - vp6 was transformed into e. coli bl21 ( de3 ) and induced with iptg. not only a fusion protein about 45ku as we expected was found but also several smaller polypeptides were observed

    組質粒pmd18 - t ? vp6上將vp6基因亞克隆到體質粒pet - 30a ,轉化大腸桿菌bl21 ( de _ 3 ) , iptg誘導以後達出預計的45ku的融合蛋白,同時還有一些小的蛋白達出來,光密度掃描對達產物進行初步定明, 45ku融合蛋白占菌體總蛋白的26 . 5 。
  16. In order to know whether the hau3r gene amplified by pcr had its natural activities, hau3r gene from phz2055 was cloned into phz1060, a streptomyces - e. coli bifunctional expression vector, to give phz2057. when e. coli dh5 a ( phz2057 ) was induced at 42c, large amounts of hau3r protein were produced to form inclusion bodies

    將來自phz2055的hau3 ~ r基因克隆到大腸桿菌?鏈黴菌雙功能體phz1060的啟動子p _ r下游的xba和ecor之間,獲得組質粒phz2057 ,經熱誘導hau3 ~ r基因超達但仍以包含體形式存在。
  17. The fifth chapter experiments on the cushioning performance of the three sets of systems with pid / pdf algorithm. mainly on how to influence the systems cushioning performance while changing the preset input signal frequency and the load mass. and on the systems " repeatability. reappearance and the stability. additionally this chapter compares the pid algorithm with the pdf algorithm in their influence on system cushioning performance. the final experiment results testifies that the thesis successfully realizes the expected cushioning effects of the three different sets of high - speed pneumatic system

    第五章對pid 、 pdf控制策略系統緩沖性能進行了實驗研究,主要研究了給定輸入信號頻率的改變對系統緩沖性能的影響、長時間工作時系統的復性和再現性以及不同負下系統的緩沖性能的實現;同時比較了pid 、 pdf控制策略對系統緩沖性能的影響。最後實驗結果明,本課題用pid 、 pdf策略很好的實現了三套不同類型的高速氣動系統的緩沖,緩沖效果是很不錯的。
  18. In this study, pichia pastoris system had been utilized for expression of fmdv 2c3abc gene which aimed for establishing a sensitive and specific molecular dignosis method. first, 2c and 3abc genes were amplified individually from p2 and 3abc postive clones and ligated together using pcr method, then this 2c3abc product was cloned into pgem - t easy vector and transformed e. coli dh5a competent cell. a postive recombinant plasmid which contained whole 2c3abc gene had been confirmed by pcr, enzyme digestion and sequencing. after that, the 2c3abc gene was sub - cloned into ppiczaa expression vector and transformed e. coli dh5 a competent cell and selected by zeocin ? antibiotic. the postive recombinant expression vector was linerized and electro - transformed pichia pastoris smd1168 competent cell. a recombinant pichia pastoris had been obtained by zeocin ? antibiotics selection and induced with 0. 5 % methanol for target protein expression. the expression product was analysised by sds - page and western blotting assay. the result sh owed that 2c3abc gene was expressed successfully in pichia pastoris and the product was a 95ku fusion protein which could be recognized by anti - fmdv serum. the amount of target protein was over 15 % of the total bacteria protein by gel thin layer scanning analysis. this research had supplied materials for establishing a fmd diagnosis method to differentiate infected animals from vaccinated animals

    首先,用p2和3abc陽性克隆通過連接pcr方法獲得目的基因並將其克隆到pgem - teasy體上,並轉化e colidh5a感受態細胞中,經pcr 、酶切以及測序證明得到了完整的2c3abc基因,並與國內外參考序列進行比較分析。然後,將目的基因亞克隆于ppiczaa體並轉化大腸桿菌dh5a ,以zeocin ~ ( tm )抗性篩選陽性克隆,大提取達質粒並用pme酶線性化后電轉化入畢赤酵母smd1168感受態細胞,通過zeocin ~ ( tm )抗生素梯度濃度篩選,獲得組酵母用0 . 5甲醇誘導達,通過sds - page電泳、 westernblotting分析,結果明, 2c3abc基因在畢赤酵母中成功達,其達產物為一95ku的融合蛋白,並能被口蹄疫病毒陽性血清識別。
  19. I preceded by an appropriate heading consisting of the words ingredients, composition, contents or words of similar meaning, the ingredients shall be listed in descending order of weight or volume determined as at the time of their use when the food was packaged

    I須冠以適當標題,標題中須有「配料」 「成分組合」 「內含物質」的字樣或具類似意思的文字,而各種配料須按其用於食物包裝時所佔的或體積,由大至小依次列。
  20. Pressure gauges of the comprehensive heavy duty range are manufactured on the basis of the modular construction system which brings advantages of quality and price

    壓力廣泛應用於製造業基於模塊化的構建系統,帶來質和價格上的優勢。
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