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pcr analysis造句

"pcr analysis"是什麼意思  pcr analysisの例文  
  • Studies on cultivar classification of osmanthus fragrans by issr - pcr analysis
  • After that we determined the presence of angiostatin gene in the putative recombinant virus with pcr analysis
  • 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
  • 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
  • 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
  • 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
  • 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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