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pcr analysis造句

"pcr analysis"是什麼意思  pcr analysisの例文  
造句與例句手機版
  • Studies on cultivar classification of osmanthus fragrans by issr - pcr analysis
    技術在桂花品種分類研究中的應用
  • After that we determined the presence of angiostatin gene in the putative recombinant virus with pcr analysis
    之后利用pcr分析是否獲得重組angiostatin的桿狀病毒。
  • 2 . 3 gene expression identification of neural related genes by semi - quanti - tive rt - pcr analysis
    3半定量rt - pcr在mrna水平檢測escs 、神經干細胞及神經細胞相關基因。
  • Rt / pcr analysis showed that ams gene expresses in leaves , stems and flowers . the expression was n ' t detected in roots
    Rt pcr分析表明ams基因在葉片、莖和花中表達,而在根中沒有表達。
  • Rt - pcr analysis was used to determine the levels of grp78 and grp94 mrna during the different phase of mouse development 2
    Rt - pcr方法檢測發育不同時期小鼠胚胎腦組織中grp78 、 grp94mrna表達情況2
  • Pcr analysis and southern blotting all confirmed that the ced - 9 gene has been integrated into the chromosomal dna of these transgenic plants
    對所得到96株再生苗進行pcr檢測,結果表明,陽性苗比例為34 。
  • Given limitation existing in all those methods , pcr analysis , an efficient method for rapid screening and diagnosis , has been used more and more
    因此,目前作為快速篩查和診斷的另一種有效方法? ? pcr分析方法? ?正在越來越多地被應用。
  • Pcr analysis showed rip gene has integrated into rice genome primarily . the positive tran - sgentic plants with lba4404 ( p3301rjp ) is dongnongv - 10 2 and fushiguang 2
    Lbamp330lrip )轉化水稻的pcr檢測陽性株數為:東農v102株,富士光2株。
  • Purple clones were picked out from the plate , which show br was expressed . pcr analysis told us that the mutant br gene was transformed into l33
    Br基因的定點突變改造和突變基因在嗜鹽菌中表達系統的建立使我們可以研究br的各種突變蛋白。
  • Gus examinaton showed that the rate of transgene was higher . and pcr analysis , pcr - southem and southern analysis all showed that chs was intigrated into quamocliy pennata chromosome successfully
    同時,還以dig標記的camv35s上的一段為探針進行southern點雜交和pcr - southern雜交。
  • It's difficult to see pcr analysis in a sentence. 用pcr analysis造句挺難的
  • Pcr analysis of resistant seedlings with nptii gene primers showed that 6 out of 12 seedlings detected had the 700bp fragment specific to the plasmid pig121 , indicating that t - dna had been integrated into the genome of sweet cherry
    L ,負壓的適宜處理是lmmxio次。 6 、通過p r擴增,初步證明證明外源基回己轉入甜櫻桃。
  • Restriction enzyme digestion analysis and pcr analysis showed that these two plant expression vectors constructed were correct . 49caixin , one cultivar of the brassica campestris l . ssp . chinensis , was transformed by vacuum infiltration method
    通過真空滲入和花序浸漬法,將上述雙抗和單抗基因分別導入白菜不結球類型? ? 49菜心中,獲得了7棵抗性株。
  • Northern blot and rt - pcr analysis show that sh2a gene is ubiquitously expressed in many tissues with three transcripts . the aberrant expression of sh2a gene in some cancers was found . it suggests that sh2a gene relates to tumors
    Rtpcr及northern印跡雜交發現sh人在多種組織中有表?二?達,有3個轉錄本,而且在癌及癌旁組織的比較中發現,腫瘤組織中表達較高,初步證明與腫瘤的發生有關。
  • As sampling of bioaerosols in natural environments is likely to be associated with substantial contamination by a range of microorganisms commonly existing in an ambient air , an investigation of the specificity of detection by targeted pcr analysis is required
    于真實環境中采樣生物性氣膠往往會被一般大氣中常存之優勢微生物所污染,故需針對特定微生物發展其特定聚合酵素反應技術相關條件。
  • Pcr analysis showed that approximate 9 % tested plants produced the target band . a few of the 9 % plants produced the band in southern blot analysis . additionally , the number of inserted copies of dsg 10 was different in different transgenic plants
    結果顯示有9的再生苗為pcr陽性,對pcr檢測陽性苗進行southem雜交分析,發現dsg10已整合入煙草的基因組中,而且在這些苗中dsg10片段整合的拷貝數不同,部分pcr陽性苗southern雜交結果卻是陰性。
  • There are four imperfect repeats v - v - e - k - k - n / e - e of which the core sequence is similar to map ib of mouse . rna blot and rt - pcr analysis showed that this gene is expressed specifically in the mature pollen and can be classified as a late gene in pollen development
    計算機軟件分析st901基因核苷酸、氨基酸序列的相似性,結果表明, st901基因編碼區與探針sb401 、與高賴氨酸基因sblr 、與番茄tsb具有較高的相似性,它們可能來源于馬鈴薯的一個基因家族。
  • Northern blot and rt - pcr analysis verified that the expression level of ldplcl was induced in germinating pollen , whereas ldplc2 expression level did not change during pollen germinating process . the interaction between heterotrimeric g proteins and plc was detected in a yeast two - hybrid system
    Northern和rt - pcr分析,發現隨著花粉的萌發, ldplc2的轉錄活性提高,而ldplc1博士學位論文在萌發前后的轉錄水平沒有變化,推測至少ldplcz參與了對花粉萌發的調控。
  • Pcr analysis indicated that all lines had been integrated of ssmapkk . northern analysis revealed the presence of expression of ssmapkk mrna in transgenic lines . in principle , ssvp overexpression can increase proton electrochemical gradients across the vacuolar membranes , which permit the secondary active transport of na + and solute molecules
    理論上, ssop的過量表達可增加轉基因植株細胞跨液泡膜的質子電化學梯度,為次級轉運提供驅動力,從而增加可溶性物質和na十向液泡內的轉運,提高轉基因植株的抗旱和抗鹽性。
  • 4 . after having established genetic transformation system with tomato cotyledons as explant and determined the transformable of preculture time , incubation time and co - culture time , we set up the system of high frequency transformation of tomato cotyledons . then hbmp - 3m gene was transferred into tomato via agrobacterium - mqdiated transformation , and the resistant plants to hyg were obtained . by pcr analysis on part of the putative transformants , we identified that hbmp - 3m gene had been integrated into the genome of part of tomato plants . 5 . transferred hbmp - 3 gene into tobacco via agrobacterium - mediated transformation and obtained the resistant plants to hyg . trans genie tobacco plants were confirmed by instantaneous expression of gus gene in calli detection , growth and bio - morphology analysis , hyg - resistant experiment and pcr analysis
    通過pcr檢測證實部分番茄抗性植株中已導入hbmp - 3m基因;人骨形成蛋白一3成熟膚基因和全長基因分別轉化番茄和煙草的研究5 .通過農桿菌介導法將hbmp一3全長基因導入煙草,并且獲得了hyg抗性植株,通過gus基因瞬時表達檢測、轉化植株的生長情況及形態學分析、 hyg抗性鑒定及pc尺檢測,證明目的基因己經整合到煙草基因組中。
  • The engineering bacterium which carried bcih i - chi and i - glu cdna was pcg - ii . two methods of agrobacterium - mediated and gene gun were used to transformate long ya lillium . the results of pcr analysis and southern dot blotting hybridization demonstrated that the chi a nd glu cdna have been intergrated into host genome . at the same time ; compared agrabactenum - mediated method with gene gun method , the transformation frequency of the former was 16 . 7 % , while the latter was 50 % , so gene gun transformation method was suitable for long ya liiliwn
    用攜帶有幾丁質酶基因和- 1 、 3葡聚糖酶基因的工程菌,通過農桿菌介導法和基因槍轉化法轉化龍牙百合,經pcr和點雜交檢測證明外源基因已經整合到植物染色體中。同時對農桿菌介導法和基因槍法進行比較,發現農桿菌介導法的轉化率為16 . 7 ,基因槍法的轉化率為50 ,因此可能基因槍轉化法更適于龍牙百合的遺傳轉化。
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