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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
631. Smaller band appear under Main product with every primers sets from PCR - (reply: 3)
632. Saliva and GCF DNA purification - (reply: 1)
633. rtPCR working but the elongated product wont gel! - (reply: 1)
634. another primer dilution question - (reply: 2)
635. TaqMan qPCR low-template issues - (reply: 1)
636. qPCR standard curve slope (m) - (reply: 2)
637. 16s double bands obtained-why?? - (reply: 2)
638. Application of RNase - (reply: 3)
639. i need help with virus pcr - (reply: 2)
640. Primer Efficiency - (reply: 2)
641. data analysis for RT_PCR - (reply: 4)
642. Experimental set up for qRT PCR - (reply: 13)
643. What temp the lid of the thermocycler must be set? - (reply: 1)
644. How should I optimize my PCR - (reply: 2)
645. Real time data analysis using 2 machines - (reply: 3)
646. Second round of PCR after gel extraction fails miserably - (reply: 3)
647. urgent help plz with RT-PCR - (reply: 3)
648. having nice sharp bands in PCR but no signal in Real-Time PCR - (reply: 5)
649. LightCycler 480 Melting Curve Assay - (reply: 1)
650. Problems with two step RT-PCR - (reply: 2)
651. Spliced and unspliced form of a gene - (reply: 3)
652. primer dilutions - (reply: 4)
653. Genotyping PCR primers - (reply: 1)
654. Standard curve using plasmid - (reply: 1)
655. How to compare these results? Please comment. - (reply: 5)
656. Primers too dilute - (reply: 1)
657. Amplification curves jagged - (reply: 1)
658. ddCT issue: no endogenous expression in control. - (reply: 4)
659. Convering 1:5 serial dilutions to logarithm scale for efficiency curves - (reply: 3)
660. No PCR product in site-directed mutagenesis - (reply: 4)