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