Conclusions: Using PCR amplification products to prepare gene chip probe was a quickly, simple effective method.
结论：利用PCR扩增产物制备基因芯片探针是一种快速、简便、实用的方法。
CONCLUSIONS HBV DNA extracted from clinical samples were directly detected using PNA biosensor and PCR amplification was successfully bypassed.
结论利用肽核酸生物传感器成功地绕过了PCR扩增而直接检测出了临床标本中的HBV基因组dna。
Conclusion: By co amplification using fluorescently labeled STR primers and detecting using PE310 genetic analyzer, the PCR products of these nine loci can be significantly distinguished.
结论：采用荧光标记引物进行复合扩增，结合PE310遗传分析仪自动分析，可以有效地区分各位点的扩增产物。
Objective To study the fetal DNA in maternal plasma using multiplex PCR amplification of the short tandem repent (STR) systems.
目的采用短串联重复序列（STR）多态位点的复合扩增方法，研究孕妇血浆中胎儿DNA基因型。
Objective To study the fetal DNA in maternal plasma using multiplex PCR amplification of the short tandem repent (STR) systems.
目的采用短串联重复序列（STR）多态位点的复合扩增方法，研究孕妇血浆中胎儿DNA基因型。
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