核性別鑒定 的英文怎麼說

中文拼音 [xìngbiéjiàndìng]
核性別鑒定 英文
nuclear sexing
  • : 核構詞成分。
  • : Ⅰ名詞1 (性格) nature; character; disposition 2 (性能; 性質) property; quality 3 (性別) sex ...
  • : 別動詞[方言] (改變) change (sb. 's opinion)
  • : Ⅰ名詞1 (鏡子 古代用銅製成) ancient bronze mirror2 (可以作為警戒或引為教訓的事) warning; objec...
  • : 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...
  • 鑒定 : 1 (評語) appraisal (of a person s strong and weak points) 2 (評定) appraise; identify; auth...
  1. Constructing human colorectal cancer cell line with stably down - regulated grp94 ( 1 ) the plasmid prc / rsv - ribol that contains specific grp94 - targeting ribozyme and the control plasmid prc / rsv were miniprepared, respectively, cleaved by endoenzyme pvuii

    下調grp94的人大腸癌細胞克隆株的構建( 1 )分對含有特異打靶grp94酶的質粒prc rsv - ribo1和對照組質粒prc rsv進行小量提取、 pvu酶切
  2. In this paper, first strand cdna of 3abc gene was synthesized using template rna extracted from cells infected with fmdv. the complete 3abc gene about isoobp was amplified by pcr and ligated into pgem - t easy vector. after transforming e. coli dh5 a, ampicillin resistant colonies were isolated and plasmid dna was prepared and analyzed by restriction analysis and pcr. presence of the full length 3abc gene was verified by nucleotide sequence analysis and the plasmid containing the expected sequence was named as pgem - 3abc. comparing the aquired sequence of 3abc with that of reference strains, the homology is more than 99 percent. the pgem - 3abc was digested with sal i and bgl ii and ligated into xho i and bgl ii - digested expression vector ptriex - 4 neo. lt was identified by restriction analysis and pcr and sequencing that this fragment had a 17bp deletion hi the nucleotide sequence 708bp of 3abc gene, which happened to form a terminator codon behind 3ab gene, but it contained the complete open reading frame ( orf ) of 3ab gene. positive clones were selected and induced with lmmol / l isopropyl - d - galactoside ( iptg ), bacteria were detected by sds - page and western blotting after properly treated. the results showed that the 3ab gene expressed successfully in e. coli and 33. 5ku fusion protein can be recognized by the positive bovine serum of fmdv. the amount of target protein is over 26 % of the total bacteria protein by gel thin layer scanning analysis

    擴增產物連接到pgem - teasy載體中,轉化大腸桿菌dh5菌株,篩選氨芐青霉素抗菌落,提取質粒經酶切、 pcr分析以及確證測序證明,所克隆的1500bp左右的片段含有完整的3abc基因,與國外參考序列相比,同源在99以上。將重組質粒pgem - 3abc和表達載體ptriex - 4neo分用sal和bgl與xho和bgl消化后,亞克隆3abc基因至原表達載體ptriex - 4neo中,通過酶切、 pcr擴增以及序列分析,發現克隆到ptriex - 4neo載體上的片段於3abc基因708bp處出現了17bp的缺失,碰巧在3ab基因后形成一終止密碼子,但3ab基因的閱讀框架完整,選出含有3ab基因完整閱讀框架的陽克隆,用iptg誘導表達,收集菌液進行sds - page電泳、 westernblotting分析,結果表明, 3ab基因在大腸桿菌中成功表達,其表達產物為分子量33 . 5ku的融合蛋白,並能被口蹄疫病毒陽血清識。經薄層掃描分析,表達量占總蛋白量的26以上。
  3. This article contains three parts, five chapters. the first part introduces the incentive models of actual bonus stock synoptically, analyses the stock on hand, option shares and stock option, the three kind of important incentive models, on rights and incumbencies, value and the incentive guidance by contrast. the second part discusses the difficulties and influential factors in the design of technical bonus stock, quests for the incentive models of technical bonus stock, analyses superiority and inferior position in action, difference and interosculation between them, discusses the need and significance for the technical bonus stock reanimation in the middle - small technicalfilms. in order to make use of the technical bonus stock distribution mechanism fully, inspire the talent of technologists, encourage their devotion to films, we have some important discussion on the technical bonus stock distribution policy, introduce the distributed models of technical bonus stock, point out the questions in the excutive course, and offer the solution correspondingly. in the third part, we discuss the technical stock option design on middle - small technical films, and consider the logical thoughtfulness in the course of reanimation as follows : the more outstanding achievement for the powered man the more increase on special target the lower price on technical option premium the more profit the more effective reanimation. in the parameter, a set of detailed program is designed, which includes establishment of incentive fund, institution of merit system for the plan ' s grantors, award of stock option, determination of premium, so as to reduce random in the incentive course, have a great effect on the mormative management for the

    本文內容共分為五章三大部分,第一部分概括地介紹了現行股權激勵方式,對現股、期股和期權這三種重要的激勵方式,從權利義務、價值和激勵導向三個方面進行了對比分析;第二部分探討了技術股權設計的難點和影響因素,討論了我國中小科技企業技術股權激勵的方式,分析它們在激勵中的優勢和不足,以及它們之間的區與聯系,並對中小科技企業實施技術股權激勵的必要和意義進行了探討。在文中還重點討論了中小科技企業技術股權分配的策略,介紹了技術股權紅利分配方式,指出在技術股權激勵過程中應注意的問題,並提出相應的解決辦法,目的在於充分利用技術股權分配機制,來激發技術人員潛在的創新能力,激勵他們為企業作貢獻;第三部分著重探討了中小科技企業技術股份期權的方案設計,在激勵方面,按照技術期權獲受人的業績越突出特的指標增長越快行權價越低獲利越多激勵效果越好的邏輯思路進行考慮;在參數設計方面,對技術期權計劃中激勵基金、授予和考、行權價格等參數進行了詳細地分析設計,旨在減少技術期權激勵過程中的隨意,為中小科技企業的規范化管理起到一的指導和借作用。
  4. The sucking mouse brain were inoculated with mdj - 01 strain to make electron microscopic examination, results showed that the virus was a spheral particle with membran which had a diameter of about 40 nm. by indirect fluorescent antibody test mdj - 01 strain was identified with tbev. a part of region encoding e protein was expanded by rt - pcr and sequenced. the nucleotide sequences of two strain viruses were compared with sequences in genbankjsequence homology analyses revealed mdj - 01 strain and senzhang strain had the highest homology with tbev oshima5 - 10, respectively, which were 95 %, 94 %. mdj - 01 strain was identified with tbev again

    應用間接免疫熒光試驗進行血清學,結果表明mdj - 01株為tbev 。通過rt - pcr技術擴增部分e蛋白序列並測序,在genbank上進行同源比較,發現mdj - 01株和森張株與tbevoshima5 - 10株的同源最高,分為94 、 95 ,從分子生物學水平上進一步證明mdj - 01株病毒為tbev 。在的基礎上,本實驗對兩株病毒進行了苷酸全序列測
  5. This article introduces the process and requirements of detection set by iaea in the light of the need for detection, setting of investigation levels and alarm threshold, selection of instrument, location and evaluation of radioactive materials

    本文從探查需求分析、調查水平和報警閾的確、儀器選擇、探測報警、位、等幾個方面介紹了對非法運輸放射物質進行探查的一般過程和要求。
  6. Nonradioactive nucleic probe to tgev was prepared and was applicated to detect tgev at first stage, which established foundational work for differentiating tgev from prcv and investigation on epidemiology of tgev

    制備了tgev非放射標記的酸探針,並初步應用於檢測tgev 。二者為tgev診斷、血清學調查奠了基礎。
  7. These include cell growth characteristics, expression levels, intracellular and extracellular expression, posttranslational modifications, and biological activity of the protein of interest, as well as regulatory issues in the production of therapeutic proteins. in addition, the selection of a particular expression system requires a cost breakdown in terms of process, design, and other economic considerations. section i : construction of pet22b ( + ) / hpk - 5 vector the hpk - 5 gene encoding 82 amino acid residues from c462 to c543 was recombined with the sequence of plasmid pet22b ( + ) for constructed a new expressed vector pet / hpk - 5

    方法在對hpk - 5 ( humanplasminogenkringle5 , hpk - 5 )因子的基因序列和蛋白質序列進行分析的基礎上,利用pcr技術分構建其可溶表達載體和不溶表達載體;用pcr快速檢測法及其基因測序儀測序以pet22b hpk - 5和pbv220 hpk - 5重組質粒,用不同的感受態大腸桿菌( e
  8. This article try to use theory and practice of difference brand to establish a health - care food brand, analysis difference brand - position, abstract core - value, establish brand - identify, make difference brand work plan, research on brand - position, core - value management and brand - identify, offering a way to help those enterprise confront morass on manage brand stratagem this article emphasis on that analysis environment of enterprise, analysis customer, product and competitive, to implement difference brand - position base on brand ' s functionality and sensibility difference, and apply difference brand - position to actualize brand ' s core - value by product - identify, enterprises - identify, individuality - identify and symbol - identify, make a plan of difference work, ultimately achieve a specific position to suit target customer

    本文主要針對企業在實施品牌差異化戰略過程中,品牌差異化位以及與此密切相關的品牌心價值管理和品牌識管理的基本理論和方法展開嘗試研究,通過筆者為一個保健品品牌實施品牌差異化的研究案例,將品牌差異化戰略的理論和實踐密切結合,分析品牌差異化位、提煉品牌心價值、建立品牌識體系、制完整的品牌差異化推廣方案,力圖為面臨品牌創建困境的企業提供一條可借的思路。
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