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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
661. After I run my pcr on agarose the DNA is still in the well - (reply: 3)
662. Need help for PCR - (reply: 5)
663. scorpion probe - (reply: 8)
664. Too low Ct value for reference gene !!! - (reply: 3)
665. unespecific band PCR from mouse genomic DNA - (reply: 9)
666. Help with primer design through PRIMER3 - (reply: 4)
667. Help with unknown band in restriction digest - (reply: 1)
668. how to chose right subsequent for her2(erbb2)gene ? - (reply: 3)
669. 454 sequencing - (reply: 2)
670. Preference for larger of 2 bands? - (reply: 2)
671. Tm of primers - prediction and verification - (reply: 1)
672. acceptable variation for biological replicate - (reply: 2)
673. RT-PCR contamination in negative control. - (reply: 1)
674. PCR malaria diagnosis nested PCR smear and non specific bands - (reply: 3)
675. Technical problem with ABI7300 - (reply: 4)
676. cdna synthesis - (reply: 1)
677. how to do RT-PCR for16srRNA of a certain bacteria? - (reply: 4)
678. Help with primer design - (reply: 3)
679. SPUD Assay Standard Curve "bell-shaped" - (reply: 5)
680. PCR smearing and...problems! - (reply: 7)
681. Message Amount in qPCR - (reply: 1)
682. Running Primers on Agarose Gel - (reply: 6)
683. Explanation needed for melting curve - (reply: 3)
684. cDNA concentration of qPCR - (reply: 1)
685. pGEX vector - (reply: 2)
686. will the template of PCR be added A ? - (reply: 2)
687. qPCR normalization of reference gene - (reply: 1)
688. Primer design: Tm above or below Ta? - (reply: 5)
689. Design primers for expression cloning - (reply: 11)
690. Designing a synthetic gene to serve as the positive control for two separate PCR - (reply: 5)