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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
601. Tm variation - (reply: 1)
602. PCR with more than one primer - (reply: 1)
603. RAPD - PCR problem - (reply: 5)
604. Relative fold expression and Normalization fold expression - (reply: 2)
605. Strange Bands - (reply: 2)
606. Recommended tamplate DNA concentration for qPCR - (reply: 2)
607. RT / cDNA synthesis - (reply: 7)
608. How to best store PCR product? - (reply: 2)
609. smearing below band of interest - (reply: 5)
610. RT-PCR primer design - (reply: 1)
611. After PCR, One Band on 1.2% Agarose but 2 bands on 8M Urea, 8% PAGE - (reply: 1)
612. Odd gel run following PCR - (reply: 28)
613. Qiagen PCR Array Reagents? - (reply: 1)
614. Enough checks for gDNA contamination in qPCR? - (reply: 3)
615. plate stuck in ABI7300 - (reply: 7)
616. No or very weak band using 16s primers - (reply: 1)
617. No PCR amplification with b-actin primers - (reply: 1)
618. Is PCR efficiency higher if mutation is in the middle of primer? - (reply: 7)
619. optical qPCR plates - (reply: 1)
620. Fold change significance - (reply: 2)
621. No PCR amplified with long primers - (reply: 10)
622. How many real time-PCR reactions for statistics and how? - (reply: 4)
623. PCR optimization: PCR vs qPCR - (reply: 4)
624. PCR smear for genomic samples - (reply: 4)
625. Smaller band appear under Main product with every primers sets from PCR - (reply: 3)
626. Saliva and GCF DNA purification - (reply: 1)
627. rtPCR working but the elongated product wont gel! - (reply: 1)
628. another primer dilution question - (reply: 2)
629. TaqMan qPCR low-template issues - (reply: 1)
630. qPCR standard curve slope (m) - (reply: 2)