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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
631. RT-PCR primer design - (reply: 1)
632. After PCR, One Band on 1.2% Agarose but 2 bands on 8M Urea, 8% PAGE - (reply: 1)
633. Odd gel run following PCR - (reply: 28)
634. Qiagen PCR Array Reagents? - (reply: 1)
635. Enough checks for gDNA contamination in qPCR? - (reply: 3)
636. plate stuck in ABI7300 - (reply: 8)
637. No or very weak band using 16s primers - (reply: 1)
638. No PCR amplification with b-actin primers - (reply: 1)
639. Is PCR efficiency higher if mutation is in the middle of primer? - (reply: 7)
640. optical qPCR plates - (reply: 1)
641. Fold change significance - (reply: 2)
642. No PCR amplified with long primers - (reply: 10)
643. How many real time-PCR reactions for statistics and how? - (reply: 4)
644. PCR optimization: PCR vs qPCR - (reply: 4)
645. PCR smear for genomic samples - (reply: 4)
646. Smaller band appear under Main product with every primers sets from PCR - (reply: 3)
647. Saliva and GCF DNA purification - (reply: 1)
648. rtPCR working but the elongated product wont gel! - (reply: 1)
649. another primer dilution question - (reply: 2)
650. TaqMan qPCR low-template issues - (reply: 1)
651. qPCR standard curve slope (m) - (reply: 2)
652. 16s double bands obtained-why?? - (reply: 2)
653. Application of RNase - (reply: 3)
654. i need help with virus pcr - (reply: 2)
655. Primer Efficiency - (reply: 2)
656. data analysis for RT_PCR - (reply: 4)
657. Experimental set up for qRT PCR - (reply: 13)
658. What temp the lid of the thermocycler must be set? - (reply: 1)
659. How should I optimize my PCR - (reply: 2)
660. Real time data analysis using 2 machines - (reply: 3)