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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
661. qPCR standard curve slope (m) - (reply: 2)
662. 16s double bands obtained-why?? - (reply: 2)
663. Application of RNase - (reply: 3)
664. i need help with virus pcr - (reply: 2)
665. Primer Efficiency - (reply: 2)
666. data analysis for RT_PCR - (reply: 4)
667. Experimental set up for qRT PCR - (reply: 13)
668. What temp the lid of the thermocycler must be set? - (reply: 1)
669. How should I optimize my PCR - (reply: 2)
670. Real time data analysis using 2 machines - (reply: 3)
671. Second round of PCR after gel extraction fails miserably - (reply: 3)
672. urgent help plz with RT-PCR - (reply: 3)
673. having nice sharp bands in PCR but no signal in Real-Time PCR - (reply: 5)
674. LightCycler 480 Melting Curve Assay - (reply: 1)
675. Problems with two step RT-PCR - (reply: 2)
676. Spliced and unspliced form of a gene - (reply: 3)
677. primer dilutions - (reply: 4)
678. Genotyping PCR primers - (reply: 1)
679. Standard curve using plasmid - (reply: 1)
680. How to compare these results? Please comment. - (reply: 5)
681. Primers too dilute - (reply: 1)
682. Amplification curves jagged - (reply: 1)
683. ddCT issue: no endogenous expression in control. - (reply: 4)
684. Convering 1:5 serial dilutions to logarithm scale for efficiency curves - (reply: 3)
685. No PCR product in site-directed mutagenesis - (reply: 4)
686. Giardia/Crypto real time PCR late amplification - (reply: 1)
687. How to dilute the template DNA for PCR - (reply: 7)
688. Desired length of overlap region for OE-PCR - (reply: 6)
689. After I run my pcr on agarose the DNA is still in the well - (reply: 3)
690. Need help for PCR - (reply: 5)