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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
631. Real time PCR sudenly not working - (reply: 1)
632. Buffer-composition One-Step RT-PCR - (reply: 4)
633. Two reverse primer sequences for a single forward primer - (reply: 1)
634. Tm variation - (reply: 1)
635. PCR with more than one primer - (reply: 1)
636. RAPD - PCR problem - (reply: 5)
637. Relative fold expression and Normalization fold expression - (reply: 2)
638. Strange Bands - (reply: 2)
639. Recommended tamplate DNA concentration for qPCR - (reply: 2)
640. RT / cDNA synthesis - (reply: 7)
641. How to best store PCR product? - (reply: 2)
642. smearing below band of interest - (reply: 5)
643. RT-PCR primer design - (reply: 1)
644. After PCR, One Band on 1.2% Agarose but 2 bands on 8M Urea, 8% PAGE - (reply: 1)
645. Odd gel run following PCR - (reply: 28)
646. Qiagen PCR Array Reagents? - (reply: 1)
647. Enough checks for gDNA contamination in qPCR? - (reply: 3)
648. plate stuck in ABI7300 - (reply: 8)
649. No or very weak band using 16s primers - (reply: 1)
650. No PCR amplification with b-actin primers - (reply: 1)
651. Is PCR efficiency higher if mutation is in the middle of primer? - (reply: 7)
652. optical qPCR plates - (reply: 1)
653. Fold change significance - (reply: 2)
654. No PCR amplified with long primers - (reply: 10)
655. How many real time-PCR reactions for statistics and how? - (reply: 4)
656. PCR optimization: PCR vs qPCR - (reply: 4)
657. PCR smear for genomic samples - (reply: 4)
658. Smaller band appear under Main product with every primers sets from PCR - (reply: 3)
659. Saliva and GCF DNA purification - (reply: 1)
660. rtPCR working but the elongated product wont gel! - (reply: 1)