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Thanks for the great video. Would you please share the reference for the formula?
If you would use a PCR thermocycler, why not set the temp to 4 degrees and then up to 16, and then cycle down again for a few cycles? Wouldnt that give the best results..?
My DNA is in TE buffer..Must I use water in my ligation reaction?
Thanks for the great video. Would you please share the reference for the formula?
If you would use a PCR thermocycler, why not set the temp to 4 degrees and then up to 16, and then cycle down again for a few cycles? Wouldnt that give the best results..?
My DNA is in TE buffer..Must I use water in my ligation reaction?