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

• With the improved method of ctab , the genomic dna extracted form plum and other species close to p . mume in genetic relationship could be directly used in pcr amplification , with good results obtained
  选用改良ctab法提取的梅及其近缘种的基因组dna可直接用于pcr扩增分析，且效果良好。
• Cloning , sequencing and identifying two novel cdna fragments related to chordoma are described in the first part and expression of fhit gene in chordoma is in the second part
  Dd一pcr产物应用凝胶系统分离、扫描，切下差异条带，重新进行pcr扩增纯化，扩增体系、条件同dd一pcr 。将纯化的。
• 3 characters of its sequences in the cardamine pcr technique was used to amplify its and the product was directly to be sequenced with two ways sequencing primers on sequenator
  3碎米属植物的ts序列特征采用pcr扩增，混合扩增产物在自动测序仪上双向引物直接测序，测定了碎米荞属( ca厂内。
• The main results are as below . 1 . we extracted rna from narcissus , cloned the cdna sequence of chs gene by rt - pcr and analyzed the coding sequence of gene
  主要结果如下： ( 1 )以即将开放的中国水仙的花蕾为材料，采用异硫氰酸胍-苯酚-氯仿法提取rna ，反转录成cdna后用特异引物pcr扩增出1
• The predicted bands were amplified from both to and ti generation transgenic plants by pcr , indicating that the hygromycin resistance gene ( hpt ) and svde gene were both transferred into tobacco
  Pcr扩增潮霉素抗性基因hpt和svde基因结果显示，在‘转淬回植株t斤t ；代中都分别扩增出互okb和二
• Department of physiology 8 4 . the c6 cells were cultured for 3 days , then total rna was extracted from the cultured cells . 5 . the cdna was synthesized from the above - mentioned total rna , then pcr was used
  将上述总rna反转录成cdna ，在进行pcr扩增，以确定是否有ilzrinrna与itlltna的表达： 6
• ( 2 ) at translation level plant mutual sequence of starting translation aaca was added to start codon of t - pa gene by pcr ampliation and plant expression vector pbet was constructed
  ( 2 )在翻译水平上通过pcr扩增的方式在t - pa基因起始密码子处添加了植物翻译起始共有序列aaca ，构建了植物表达载体pbet 。
• The two genes were in an open reading frame . the fragment of pro3a + crylac10 without terminated structure was inserted into plasmid pbmb1205 when it was digested by bamhi and sphi
  首先pcr扩增去掉终止结构的pro3a + cry ac10片段，用bamh 、 sph酶切pcr产物插入到解离载体pbmb1205上得到中间载体pbmb1205ac 。
• 2 ) screening using pcr . sequencing of pgex - hbrp the plasmid was screened by pcr , and 1 % agarose gel electrophoresis . the results show that there was one band at the respected sites about 750bp
  2 ) pcr鉴定经过双酶切鉴定的质粒dna用pcr扩增，结果可见，在750bp处出现明显的带，表明插人的片段确是外源
• A 358 bp pol ft cdna fragment framed with introduced restrict sites of xho i ( upstream ) and nhe i ( downstream ) was amplified by the method of rt - pcr , and then cloned into a ta - vector
  Rt一pcr扩增得到358hp的pcilpcdna片段，并在其上下游引物中分别引人了h 。 i和ie内切酶位点。 l此片段克隆人ta克隆载体后，经h 。