pcr扩增的英文

• pcr amplification

• pcr    PCR ＝polymerase chain reacti ...
• 扩    expand; enlarge; extend
• 增    increase; gain; add
• 扩增    amplification; augmentation; pcr
• 等位特异性pcr,等位基因特异性扩增技术    allele specific pcr
• as-pcr    等位基因特异性多聚酶链反应
• pcr    PCR ＝polymerase chain reaction 【生物化学】聚合酶联锁反应〔此项技术可用以复制犯罪现场发现的DNA小样，从而有助于破案〕。
• dna 扩增    dna amplification
• dna扩增    dna amplification
• rdna 扩增    rdna amplification
• rdna扩增    rdna amplification
• 扩增子    amplicon
• 酶扩增    enzymatic amplification
• add-on pcr    加端pcr
• alu pcr    alu聚合酶链式反应
• anchor pcr    锚定pcr
• anchored pcr    锚式聚合酶链（式）反应，锚式pcr; 锚式聚合酶链反应; 锚式聚合酶链式反应
• asymmetric pcr    不对称pcr
• competitive pcr    竞争（性）
• degenerate pcr    退化性聚合链反应
• hbv-pcr    乙肝病毒
• in situ pcr    原位聚合酶链式反应
• inverse pcr    反向聚合酶链反应; 反向聚合酶链式反应
• irs-pcr    pcr]技术; 散在重复序列pcr[整条染色体基因组dna; 散在重复序列pcr技术
• lm-pcr    连接反应介导的pcr

• The fragments of gapdh gene and the potassium channel gene were amplified using the genomic dna of the four animals as a template
  以基因组dna为模板，进行pcr扩增。扩增gapdh基因片段的大小约为300bp ，扩增钾通道基因片段的大小约为940bp 。
• Search the snps in wnk4 genomic sequences design the primers to get the unique pcr products of wnk4 gene which cover the full length genomic sequences
  Dna的pgem一t载体为模板，用含有ha标签及酶切位点的上下游引物进行pcr扩增，酶切pedna3
• When plants were grown , dna were extracted and transgenic lettuce plants were identified by pcr amplifying . seeds of transgenic plants were obtained . 4
  本论文中获得的再生生菜植株通过gus染色和pcr扩增，证明导入了外源mbrazzein基因。
• 2 . ginlfyand ginndly gene were obtained from the leaf genomic dna of the male tree of ginkgo cultivar dafushou in the mid - april through pcr
  Dafushou )雄株基因组dna为模板，通过pcr扩增，获得两个银杏雄株leafy同源基因ginlfy和ginndly基因。
• Detection of transgenic plants . the pcr assay of kan - resistant plants showed that the target gene had been integrated into tobacco accompanying with npt ii gene
  转基因pcr检测pcr扩增npt11基因，证明thaumatin基因己导入烟草中，转化率为引
• 4 . genomic dna was extracted from some animal products provided by nanjing customs . partial mitochrondrial dna cytochrome b ( cyt b ) gene was amplified and sequenced
  对南京海关送检的部分动物产品进行基因组dna提取， mtdnacytb基因的中文摘要pcr扩增和序列测定。
• Confirmation of transformant . integration of sag - ipt into chrysanthemum genome was confirmed in two thirds of the putative tansgenic plantlet be pcr amplification
  通过pcr扩增表明，转基因植株中可以检测出有目的基因( ipt基因)的存在，目的基因已成功地插入菊花的基因组中。
• Through in situ hybridization and colony pcr , a positive recombinant plasmid was isolated from the genomic library and sequenced . the inserted dna fragment was about 4 . 3 kb
  将pcr扩增片段用地高辛标记探针，利用原位杂交和菌落pcr从基因文库中获得含有阳性信号的重组质粒。
• On the base of construction of pbi121vp7 , we constructed the fusion gene expression vector pbi121ctbvp7 by the same sigle cloning site ( ndei and xbai ) of vector puc19ctb and pbi121vp7
  设计具有ndei和saci单限制性酶切位点的vp7基因引物，通过pcr扩增出vp7基因并经测序验证。
• Plant defensin afp ( 238bp ) was amplified with six long complementary primers after two rounds of pcr amplification and plant expression vector peafp was constructed . 3
  通过合成六条长链引物，经两次pcr扩增，获得了238bp的植物防御素afp基因全长，并构建了植物表达载体peafp 。