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寡核的英文

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"寡核"怎么读用"寡核"造句

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  • oligonucleotide

例句与用法

  • The accuracy and stability of the typing result typing results match the set results , and in 5 hybridization , the repeated rate is 91 . 2 %
    3寡核营酸芯片分型结果的准确性与稳定性分型结果与dna测序相符合,重复5次杂交重现率91 . 2 % 。
  • Then hydrate and roast " to fix the probes , ready for use 6 . block and hybridizate block and wash the prepared slides by the method developed in our lab
    6 .封闭与核酸分子杂交按本室方法,将制备好的寡核昔酸微阵列,清洗,封闭。
  • 2 . the optimize of the oligonucleotide probes preparation the optimal condition is to resuspend the probes in ph = 9 , 0 . 1 m carbonate buffer to 100 m . 3
    2 .寡核昔酸探针制备条件的优化以ph二9 , 0 . im的碳酸盐缓冲液,重悬为100林m探针为最优条件。
  • These results show that cdna expression library has an excellent quality and lays solid foundation for further screening . in addition , the library is also used for screening other breast cancer relevant genes
    同时由于该文库包含了此乳腺癌细胞系的全部基因信息,因此也可以用其他的抗体或寡核昔酸探针筛选乳腺癌的相关基因。
  • Then the effect of turning channel has been studied . 7 . this detection system has been used to dna segments separation experiments ; the results showed that it has met the need for dna separation
    将该微通道电泳芯片系统应用于不同荧光标记寡核苦酸、 dna片段的分离分析,实现了寡核着酸的单碱基分辨,同时应用于结核杆菌基因组pcr产物的分析,实验结果表明此系统可以实现dna片段的快速高效分析。
  • 5 . prepare the oligonucleotide microarray add 16 prepared probes into 384 - pole plate , meantime , add p2 , low homologic probes and probe buffer in the same concentration as positive control , blank control and negative control respectively . spot microarray as designed by the spotting machine
    5 .寡核昔酸微阵列的制备以同等浓度的反义链引物咫作为阳性对照,以探针缓冲液作为空白对照,以无关探针作为阴性对照,与制备好的16条寡核昔酸探针,同时加人384孔板。
  • The effects of glp - 1 ( 7 - 36 ) nh2 on insulin secretion glp - 1 ( 7 - 36 ) nh2 with the concentration of 2 . 5nmol / l , 5 . . 0nmol / l , l0 . 0nmol / l , 20 . 0nmol / l , 40 . 0nmol / l respectively were added to the medium as different experimental groups , 24 hours later , insulin amount are 68 . 76 ? 1 . 71 72 . 30 ? 3 . 13 104 . 16 ? 5 . 57 110 . 98 ? . 29 111 . 58 ? 0 . 65miu / l respectively , and the insulin account is 55 . 53 ? . 63miu / lin the control group . there was no significant difference between the groups with 2 . 5nmol / land 5 . 0nmol / l glp - 1 ( 7 - 36 ) nh2 respectively ; and there was not significant difference among the groups with lo . onmol / l , 20 . 0nmol / l and 40 . 0nmol / l glp - 1 ( 7 - 36 ) nh2 respectively . but the difference is significant between experimental groups and control group ( p < 0 . 05 ) . the data show that with the rising concentration of glp - 1 ( 7 - 36 ) nh2 , there is an increasing amount of insulin
    对照组培养液中不含g廿一1 ( 7一36 ) nhz ,实验组培养液中含有20nmol / lglp一1 ( 7一36 ) nhz ,培养24h后,用0 . 25 %胰蛋白酶消化胰岛分散细胞,涂片后利用针对胰岛素mrna的寡核甘酸探针进行细胞原位杂交, dab显色,高清晰度病理图文分析系统( highpathologiealimageanalysissystem , hp认s )对细胞着色的平均光密度( mean即tiealdensity , mod )量化分析,观察实验组和对照组胰岛素mrna的表达情况。
  • That is to add a special fluorescence - based dna internal standard in the telomerase elongated ts primers , then do pcr amplification after a step of refinement ( hydroxybenzene / chloroform extracting , and deposited by ethanol ) . sequencing analysis of pcr product was done on 310 gene scan analysis ? . 1 . 2 dna sequencer to determine telomerase activity . notably , this method eliminated the restraining factors of taq dna polymerase , making it possible to erase the sample differences met in pcr and eradicate the annoying phenomena of pseudo negative results
    在kim等开发的端粒重复扩增分析法( trap )的基础上进行改进,即通过对端粒酶延伸ts寡核昔酸反应产物的精制,消除了pcr扩增中抑制taq酶活性的因素,从而减少了样品之间pcr扩增上的差异和假阴性现象的发生,提高了判断样品端粒酶阴、阳性的准确率和定量的准确性。
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