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