檢定標記 的英文怎麼說

中文拼音 [jiǎndìngbiāojì]
檢定標記 英文
verification marks
  • 檢 : Ⅰ動詞1 （查） check up; inspect; examine 2 （約束; 檢點） restrain oneself; be careful in one s c...
  • 定 : Ⅰ形容詞1 （平靜; 穩定） calm; stable 2 （已經確定的; 不改變的） fixed; settled; established Ⅱ動詞...
  • 標 : Ⅰ名詞1 [書面語] （樹梢） treetop; the tip of a tree2 （枝節或表面） symptom; outside appearance; ...
  • 記 : Ⅰ動詞1 （把印象保持在腦子里） remember; bear in mind; commit to memory 2 （記錄; 記載;登記） writ...
  • 檢定 : docimasy; docimasia; verification; calibration; appraisal檢定報告 probation report; 檢定滴定管 [...
  • 標記 : （標志; 記號; 貨物標記） tab; sign; stamp; peg; label; mark; flag; blip; notation; fleck; track; ...
  1. In the present study, aflp ( amplified fragment length polymorphism ) markers was used to examine population of abies yuanbaoshanensis in order to understand the level of population genetic variation and genetic structure. the result would help to evaluate its evolutionary potentiality and the degree of being endangered and could provide scientific basis for making right protection strategy. high - quality dna was extracted using ctab method from those tender leaves of forty - three fully - developed trees in population abies yuanbaoshanensis

    本研究選用一種高效的檢測遺傳變異的分子標記? ? aflp技術來分析元寶山冷杉種群的遺傳多樣性，旨在了解該種群在分佈區內的遺傳變異水平和遺傳結構情況；研究結果將有助於更清楚地認識這一瀕危類群的生存潛力和瀕危程度，而且可以為制定何種挽救和保護措施提供科學的依據。
  2. Test 3 : detected activity of serum and immunoglobulin samples by indirect elisa test, rabbit antibody against foxes ' igg and hen ' s labeled with hrp igy was used in indirect elisa test

    試驗三：間接elisa檢測的抗體活性。用過氧化物酶標記的兔抗狐igg和雞igy抗體進行間接elisa測定獲得的樣品的活性。
  3. As analyzed, ( 1 ) the rapd technique is highly sensitive to investigating genetic diversity in t. lepturus and e. muticus. t. lepturus exhibits lower polymorphism and genetic diversity than e. muticus ; ( 2 ) according to the analysis of the partial mitochondrial 16s rrna gene sequences, a very low intraspecific variation and considerably high divergence among species were found, which reveals a dual nature of conservatism and variability in mitochondrial 16s rrna gene ; ( 3 ) five primers generate the species - speeific rapd sites and these sites can be served as the molecular markers for species identification and ( 4 ) it can be proved at dna variation level that t. lepturus and e. muticus are of two species respectively pertainiag to different genera, which supported the nelson taxonomic conclusion

    分析結果表明: （ 1 ） rapd技術研究黃海帶魚和小帶魚的遺傳多樣性具有較高的靈敏度和檢出率，帶魚的多態比例和遺傳多態度均較小帶魚的低; （ 2 ）線粒體165出兇a基因序列在分析兩物種遺傳變異時表現出保守和變異的雙重特性，種內變異極小而種間較大: （ 3 ） 5個隨機引物擴增出種特異的ra衛d帶，可作為種間分子鑒定標記; （ 4 ）研究證實帶魚和小帶魚是不同屬的兩個種，從而在分子水平上支持了nelson分類系統的觀點。
  4. 7. at the first time, the reporter dye, fam was linked to the 5 " - end of the oligonucleotides of the probes, and the tamra was located at the 3 " - end as quencher dye. we use camv35s and fmv promoter, nos terminater, mark gene nptii, and aim gene pat, epsps and cryla ( b ) genes as target sequences, design pairs of sp

    7 、首次以fam熒光素標記探針5 』端作為發光基團，以tarma標記探針3 』端為淬滅基團，以camv35s 、 fmv啟動子、 nos終止子、標記基因nptll 、抗除草劑基因epsps 、 pat 、抗蟲基因cry1a ）為檢狽目標，設計、篩選出特異性引物和探針，優化實驗參數，建立了轉基因植物通用性熒光pcr定性檢測方法體系。
  5. Aiming at the calibration of traffic radar, this paper analyzed shortcomings of conventional calibration method which be used in radar speed gun calibration regulations ( jjg528 - 2004 ) and put forward two new methods to verify it and developed speed standard instrument

    摘要針對公路交通中雷達測速儀的檢定問題，分析了《雷達測速儀檢定規程》 （ jjg528 - 2004 ）中規定的檢定方法的不足之處，提出了兩種新的雷達測速儀檢定方案測試數據記錄比對法和測試數據實時比對法，並研製了相應的速度標準裝置（測速誤差0 . 5 % ） 。
  6. In this system, the movement of the step - electromotor is controlled by computer, and then the dial pointer is drove by the step - electromotor. at the same time, these images of the analog instrument are took by high precision ccd video, and then these images will be processed by the computer, using some image - processing algorithms such as image segmentations, threshold identification, image binarization, areas labeling, dial center - point identification, useful areas identification & abstracting, and areas thinning, etc. followed this, the dial pointer of the “ circle ” is able to be located. at last, the dial pointer position will be recognized by the computer

    本系統由計算機控制步進電動機的運動，進而驅動指針式儀表表針的運動，並且通過高精度ccd攝像機實時獲取表盤圖像數據，同時進行表盤圖像的相關處理，包括圖像分割，閾值確定，圖像二值化，區域標記演算法，圓心擬合，有效區域識別提取，區域細化等，最終快速識別出表盤指針所處位置;最後，根據國家指針式儀表類檢定規程所制定的演算法計算出該儀表的相關誤差，檢定指針式儀表的各種精度，通過這些數據判斷該儀表是否合格，列印該儀表的檢定結果報表。
  7. Parameters specify whether to use the big - endian byte order, whether to provide a unicode byte order mark, and whether to throw an exception when an invalid encoding is detected

    參數指定是否使用big - endian位元組順序，是否提供unicode位元組順序標記，以及當檢測到無效編碼時是否引發異常。
  8. The experimental method includes selecting pure complexes of histidine - containing or cysteine - containing materials, from c - and n - terminal group of these amino acids to link to a group which have color or fluorescence or ultraviolet absorption, elucidating their binding affinity, fluorescence or uv - visible spectrum properties with zinc at physiological concentration and to elucidate their structure in the solid state via infrared spectroscopy. with the help of the concerned the data, the analysis was done to prove whether it can be applied to the zinc detection, in other words, whether it can be used as a new fluorescence probe for zinc detection

    本實驗首次選用在生物體內與zn ~ （ 2 + ）鍵合能力很突出的物質? ?組氨酸和半胱氨酸，採用類似於多肽合成的方法，在其羧基或氨基分別嫁接上一個帶有標記的基團，生成穩定的共價鍵化合物；在此化合物中模擬生理濃度條件加入鋅離子，通過紅外圖譜、紫外圖譜或熒光圖譜的變化分析鋅離子對標記基團是否產生影響，再結合有關數據分析其是否適合檢測鋅離子，即是否可能作為新的鋅離子熒光探針。
  9. The expressed product was lysised with supersonic wave and purified by sds - page. elisa analysis revealed that the antigenicity of the vpi protein has been detected. the forth part - detection of aev - nh937 strain by in situ hybridization ( 1sh ) - probe was labelled with digoxigenin ( dig ). then the probe hybrid with 5d, 10d, and 20d postinfection brain tissue of chicken. the results of the ish showed that the positive signal was found in 3 cases, while control group was negative. there has been a reasonable correlatien between this method and other detection test

    經超聲波裂解，用尿素溶解包涵體，電泳純化后，利用elisa檢測vp _ 1外殼蛋白，表明具有一定抗原性；第四部分：應用原位雜交檢測aevi用dig標記的探針與sd 、 10d 、 20d的攻毒雞腦組織雜交，來檢測那v的rna 。
  10. Application of microsatellite dna polymorphisms and dna fingerprints to inbred strain mice and rats to screen the exact, dependable, particular genetic monitoring marker method of laboratory animal, the author had studied the application of microsatellite dna polymorphisms and dna fingerprints to inbred strain mice and rats, and compared the two methods with the biochemical marker enzyme method. the study had established the foundation of the molecular genetic monitoring marker method of laboratory animal

    本文通過對dna指紋技術和pcr擴增微衛星dna技術在近交系大、小鼠遺傳檢測中的應用研究，並與生化位點標記分析法進行比較，旨在篩選出具有精確、可靠、特異性好的實驗動物遺傳檢測方法，為建立分子生物學實驗動物遺傳質量監測技術和標準奠定基礎。
  11. Although this method gives high sensitivity, the radioactive labels present many problems such as a potential hazard to analyst and environment, which limited its application in dna diagnostic laboratories. in order to overcome these problems a serious of non - radioactive dna probes such as fluorescent, chemiluminescent and electrochemical probes have been developed. although these new methods display many advantages, they have not been used to take place completely the traditional method because of low sensitivity or complex equipment or other shortcomings

    自20世紀80年代以來，各種非同位素如酶、熒光素、生物素、地高辛標記的化學發光法和熒光分析法以及以電活性物質做標記的電化學方法相繼問世，這些方法雖然在一定程度上克服了同位素標記的缺陷，但由於存在靈敏度不夠高或檢測系統龐雜或儀器價格昂貴或標記物不穩定等缺陷，還不能完全取代傳統方法。
  12. Due to these inherent advantages, ecl method has attracted much attention from all analytical fields, especially from biochemical analysis. in this dissertation we focused on the preparation of a new type of dna probes which were labeled with ecl activated substances. based on coupling with the dna hybridization and immobilization techniques, we have developed new ecl methods for the determination of special dna sequence

    本論文通過研究了多種ecl活性物質的發光性能，並以這些物質為標記物制備了多種高靈敏度的dna - ecl探針，結合dna雜交技術和dna固定化技術，將高靈敏度的ecl檢測手段應用於生命物質dna的序列識別及含量測定，為dna傳感器的研究和基因晶元的開發提供了新的思路和方法。
  13. Compared to sensitive, stable and visible gus histological stain method, luminescent activity of luxab could not be directly detected in nodules marked with luxab

    與標記紫雲英根瘤的靈敏、穩定、可視的gus組織染色法相比，未直接檢測到luxab標記根瘤的luxab發光活性。
  14. Methods according to theory of specific binding of antigen and antibody, at first the anti - a monoclonal antibody ( ma ) and anti - bma were labeled with the fluorescent, then fluorescent - labeled antibodies ( fla ) were bound with corresponding biological material ( such as bloodstain ) in the optimum condition, finally the abo blood type of bloodstain was determined under microscope fluorescent

    方法根據抗原抗體特異性結合的原理，首先對抗a 、抗b單克隆抗體進行熒光標記，然後使熒光標記抗體與相應抗原（血痕）在最佳條件下結合，最後熒光顯微鏡鏡檢，判定血痕的血型。
  15. 6 shipyard sort out the relevant record and fill in test report after anchor equipments and windlass test. and signed by shipyard / classification society / shipowner

    每個錨鏈的標記和鏈尾固定情況應在安裝前進行檢查，棄鏈器設備的檢驗應在錨脫勾時進行。錨鏈全部收好后檢查鏈在錨鏈艙的堆放情況是否完好。
  16. Psa has been shown to be the most effective immunohistologic marker for prostate cancer, and the most useful serologic test in staging and monitoring prostate cancer and in early detection of recurrent disease

    當前研究已證實前列腺特定抗原為前到腺癌最有效之免疫組織標記，也為前列腺癌期別判定、追蹤和早期檢測腫瘤復發最有用之血清檢測。
  17. A pair of primer, dig labeled probe and a taqman probe based on the conserved nucleotide sequence of cp gene of different pnrsv strains were designed and synthesized

    本文根據病毒各株系外殼蛋白基因的保守序列，設計了雜交誘捕探針、 dig標記雜交探針以及確定了最佳誘捕參數和雜交檢測參數，建立雜交誘捕rt - pcr ? elisa 。
  18. After the estimation of labeling efficiency tp was applicated to hybridize the rna of tgev, then was subjected to self - development of x - ray exposed by cspd to show the target nucleic acid

    對標記效率測定后，以帶正電的尼龍膜為介質進行特異性和靈敏性檢測，經非放射性自顯影來顯示靶核酸。
  19. Refrigerating unit system - definitions, testing, marking

    獨立製冷系統.定義檢驗標記
  20. Sinensis and e. j. hepuensis has been found in the sequences of the portions of 16s rdna and pcr / rflp studies of 110 samples, from six river valleys in eastern mainland of china. these subspecies - specific restriction sites allow rapid discrimination with the endonuclease dra i, and therefore can be used as a diagnostic genetic marker for identification of the two subspecies

    通過對中國大陸東部6個水系110個絨螯蟹個體16srdna部分序列的測定和pcr rflp分析，發現在合浦絨螯蟹與中華絨螯蟹之間存在3 4個固定的堿基替代，這種亞摘要種特異性的限制性位點可以通過限制性內切酶dra進行快速檢測，成為2個亞種的分子鑒定標記。
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