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For running a PCR we need different components e.g. 1: PCR Master Mix 2: ddh2O 3: Forward Primer 4: Reverse Primer 5: cDNA I want to know....that what will be the consequences if we increase or...
07 July 2019 6,708 7 View
How can we correctly recognize the promoter region for a gene, specially for those genomes which are not well established and annotated? I have read on many places that its almost 2000 bp before...
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Can we extract DNA and directly use it for qPCR or it is necessary to extract RNA and then convert into cDNA and use?
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Dear fellows, I want to ask a simple question that if a person publishes a research article in 2010 and at that time the impact factor of that journal was 4 and after sometimes it decreases up...
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