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661. No or very weak band using 16s primers - (reply: 1)
662. No PCR amplification with b-actin primers - (reply: 1)
663. Is PCR efficiency higher if mutation is in the middle of primer? - (reply: 7)
664. optical qPCR plates - (reply: 1)
665. Fold change significance - (reply: 2)
666. No PCR amplified with long primers - (reply: 10)
667. How many real time-PCR reactions for statistics and how? - (reply: 4)
668. PCR optimization: PCR vs qPCR - (reply: 4)
669. PCR smear for genomic samples - (reply: 4)
670. Smaller band appear under Main product with every primers sets from PCR - (reply: 3)
671. Saliva and GCF DNA purification - (reply: 1)
672. rtPCR working but the elongated product wont gel! - (reply: 1)
673. another primer dilution question - (reply: 2)
674. TaqMan qPCR low-template issues - (reply: 1)
675. qPCR standard curve slope (m) - (reply: 2)
676. 16s double bands obtained-why?? - (reply: 2)
677. Application of RNase - (reply: 3)
678. i need help with virus pcr - (reply: 2)
679. Primer Efficiency - (reply: 2)
680. data analysis for RT_PCR - (reply: 4)
681. Experimental set up for qRT PCR - (reply: 13)
682. What temp the lid of the thermocycler must be set? - (reply: 1)
683. How should I optimize my PCR - (reply: 2)
684. Real time data analysis using 2 machines - (reply: 3)
685. Second round of PCR after gel extraction fails miserably - (reply: 3)
686. urgent help plz with RT-PCR - (reply: 3)
687. having nice sharp bands in PCR but no signal in Real-Time PCR - (reply: 5)
688. LightCycler 480 Melting Curve Assay - (reply: 1)
689. Problems with two step RT-PCR - (reply: 2)
690. Spliced and unspliced form of a gene - (reply: 3)
662. No PCR amplification with b-actin primers - (reply: 1)
663. Is PCR efficiency higher if mutation is in the middle of primer? - (reply: 7)
664. optical qPCR plates - (reply: 1)
665. Fold change significance - (reply: 2)
666. No PCR amplified with long primers - (reply: 10)
667. How many real time-PCR reactions for statistics and how? - (reply: 4)
668. PCR optimization: PCR vs qPCR - (reply: 4)
669. PCR smear for genomic samples - (reply: 4)
670. Smaller band appear under Main product with every primers sets from PCR - (reply: 3)
671. Saliva and GCF DNA purification - (reply: 1)
672. rtPCR working but the elongated product wont gel! - (reply: 1)
673. another primer dilution question - (reply: 2)
674. TaqMan qPCR low-template issues - (reply: 1)
675. qPCR standard curve slope (m) - (reply: 2)
676. 16s double bands obtained-why?? - (reply: 2)
677. Application of RNase - (reply: 3)
678. i need help with virus pcr - (reply: 2)
679. Primer Efficiency - (reply: 2)
680. data analysis for RT_PCR - (reply: 4)
681. Experimental set up for qRT PCR - (reply: 13)
682. What temp the lid of the thermocycler must be set? - (reply: 1)
683. How should I optimize my PCR - (reply: 2)
684. Real time data analysis using 2 machines - (reply: 3)
685. Second round of PCR after gel extraction fails miserably - (reply: 3)
686. urgent help plz with RT-PCR - (reply: 3)
687. having nice sharp bands in PCR but no signal in Real-Time PCR - (reply: 5)
688. LightCycler 480 Melting Curve Assay - (reply: 1)
689. Problems with two step RT-PCR - (reply: 2)
690. Spliced and unspliced form of a gene - (reply: 3)