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引物设计和Primer-BLAST的应用

Primer-BLAST 2. 3. 4. Polymerase Chain Reaction 1971 Khorana 1985 KaryMullis PCR1986 5 Mullis The Cold Spring Harbor Laboratory CSHL PCR 1. DNA PCR PCR Inverse PCR IPCR PCR anchored PCR RACE Rapid Amplification of cDNA Ends PCR ligation-mediated PCR LM-PCR 2. PCR nested PCR 3. PCR PCR real-time quantitative PCR RQ-PCR G+C 40%-60% 4 18-27 3bp 3bp 3 Tm Tm 5 C Tm 10 C3 3 G C 3 NNGC NNCG GC rich AT rich 3 T/C A/G Primer Premier 6 P6 Beacon Designer 8 DB Oligo 6 Vector NTI Suit Primer Express PCR *Omiga* serpine1 NCBI Reference Sequence: Primer Premier

附3:微滴式数字PCRDroplet Digital PCR,ddPCR) ddPCR系统在传统的PCR扩增 前对样品进行微滴化处理,即将 含有核酸分子的反应体系分成数 万个纳升级的微滴,其中每个微 滴或不含待检核酸靶分子,或者 含有一个至数个待检核酸靶分子。 经PCR扩增后,对每个微滴的荧

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Transcription of 引物设计和Primer-BLAST的应用