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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
631. RT / cDNA synthesis - (reply: 7)
632. How to best store PCR product? - (reply: 2)
633. smearing below band of interest - (reply: 5)
634. RT-PCR primer design - (reply: 1)
635. After PCR, One Band on 1.2% Agarose but 2 bands on 8M Urea, 8% PAGE - (reply: 1)
636. Odd gel run following PCR - (reply: 28)
637. Qiagen PCR Array Reagents? - (reply: 1)
638. Enough checks for gDNA contamination in qPCR? - (reply: 3)
639. plate stuck in ABI7300 - (reply: 8)
640. No or very weak band using 16s primers - (reply: 1)
641. No PCR amplification with b-actin primers - (reply: 1)
642. Is PCR efficiency higher if mutation is in the middle of primer? - (reply: 7)
643. optical qPCR plates - (reply: 1)
644. Fold change significance - (reply: 2)
645. No PCR amplified with long primers - (reply: 10)
646. How many real time-PCR reactions for statistics and how? - (reply: 4)
647. PCR optimization: PCR vs qPCR - (reply: 4)
648. PCR smear for genomic samples - (reply: 4)
649. Smaller band appear under Main product with every primers sets from PCR - (reply: 3)
650. Saliva and GCF DNA purification - (reply: 1)
651. rtPCR working but the elongated product wont gel! - (reply: 1)
652. another primer dilution question - (reply: 2)
653. TaqMan qPCR low-template issues - (reply: 1)
654. qPCR standard curve slope (m) - (reply: 2)
655. 16s double bands obtained-why?? - (reply: 2)
656. Application of RNase - (reply: 3)
657. i need help with virus pcr - (reply: 2)
658. Primer Efficiency - (reply: 2)
659. data analysis for RT_PCR - (reply: 4)
660. Experimental set up for qRT PCR - (reply: 13)