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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
1681. no pcr amplification product - (reply: 9)
1682. Primer Dimer in NTC Only? - Primers Dimers show up in NTC but not template wells (reply: 4)
1683. less steep curve and high Ct value! - (reply: 2)
1684. Question about site directed mutagenesis - (reply: 1)
1685. Amplfication of fungal DNA - (reply: 8)
1686. PCR problem - (reply: 4)
1687. mRNA level in transgene cell line or knocking down cell line - (reply: 3)
1688. differently behavioring replicates in real-time PCR - (reply: 1)
1689. Multiplex PCR - (reply: 1)
1690. No amplification in PCR using gDNA extracted from formailin fixed paraffin embed - (reply: 3)
1691. optimal template dna concentrations - (reply: 1)
1692. reconstitution of primers - (reply: 2)
1693. Mysterious PCR Contamination - (reply: 13)
1694. RT-PCR Help - Protocol provided (reply: 4)
1695. Endogenous control in bacterial RT-qPCR - (reply: 4)
1696. Mutagenesis PCR and undesired amplification - (reply: 2)
1697. PCR-how to set 'Extension: ramping from 55 to 72 for 5min' - (reply: 4)
1698. primer dimer - (reply: 2)
1699. Genotyping conditioning-where to start? - (reply: 1)
1700. Marker migrates slower depending where is loaded - (reply: 2)
1701. PCR on degraded templates - (reply: 2)
1702. PCR help needed - (reply: 3)
1703. want to purify PCR product from agarose gel but have primer dimer - (reply: 3)
1704. Tm difference - (reply: 2)
1705. Genotyping - PCR not working (reply: 6)
1706. RT qPCR Newbie, Weird Results - (reply: 1)
1707. Low qPCR efficiency with plasmid template, why? - Low qPCR efficiency with plasmid template (reply: 5)
1708. light bands, dark smear, dark dimers - (reply: 2)
1709. PCR, followed by sequencing... - why ?? (reply: 3)
1710. qPCR and varying cDNA concentrations - (reply: 1)