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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
661. PCR optimization: PCR vs qPCR - (reply: 4)
662. PCR smear for genomic samples - (reply: 4)
663. Smaller band appear under Main product with every primers sets from PCR - (reply: 3)
664. Saliva and GCF DNA purification - (reply: 1)
665. rtPCR working but the elongated product wont gel! - (reply: 1)
666. another primer dilution question - (reply: 2)
667. TaqMan qPCR low-template issues - (reply: 1)
668. qPCR standard curve slope (m) - (reply: 2)
669. 16s double bands obtained-why?? - (reply: 2)
670. Application of RNase - (reply: 3)
671. i need help with virus pcr - (reply: 2)
672. Primer Efficiency - (reply: 2)
673. data analysis for RT_PCR - (reply: 4)
674. Experimental set up for qRT PCR - (reply: 13)
675. What temp the lid of the thermocycler must be set? - (reply: 1)
676. How should I optimize my PCR - (reply: 2)
677. Real time data analysis using 2 machines - (reply: 3)
678. Second round of PCR after gel extraction fails miserably - (reply: 3)
679. urgent help plz with RT-PCR - (reply: 3)
680. having nice sharp bands in PCR but no signal in Real-Time PCR - (reply: 5)
681. LightCycler 480 Melting Curve Assay - (reply: 1)
682. Problems with two step RT-PCR - (reply: 2)
683. Spliced and unspliced form of a gene - (reply: 3)
684. primer dilutions - (reply: 4)
685. Genotyping PCR primers - (reply: 1)
686. Standard curve using plasmid - (reply: 1)
687. How to compare these results? Please comment. - (reply: 5)
688. Primers too dilute - (reply: 1)
689. Amplification curves jagged - (reply: 1)
690. ddCT issue: no endogenous expression in control. - (reply: 4)