I used barcoded primers to amplify 16s rRNA, however, no amplify in my gel with amplification just for positive control, I hope to know main reason for this.
best wishes
I have been getting smears in my negative control and clear bands in the positive control. What could be the cause?
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I am working with 16s rRNA , my amplicon size is 390 bp with 315f-806r , however I have got 350 bp , is it normal? please , if any one know answer , replay to me
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I have problem with my gel i hope to find someone to help me, there is smeared band in with amplification of S16 rNA in whole blood samples. i have put gel picture in attached file , the problem...
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It's an end-point PCR protocol. I'm using 1.5% agarose gel with SyBR Safe dye and TBE as a running buffer, visualization on BioRad XR+ system. I was primarily thinking of primer efficiency,...
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