Good day, I hope you are all doing well.

I was designing primers for Caspase 9 and sometimes, the designed primers in NCBI have transcript variants for the same gene (Caspase 9) but at the same time they have unintended templates for completely random genes, such as cyclin D, Zinc Finger proteins, protocadherin, phosphtidyl inositol, etc as well as multiple transcript variants of these. Why does this happen?

I assume that you should only pick the ones that are transcript variants for your own gene of interest for gene expression?

Is it because the primer combination can also bind to these random genes?

The primers are for quantitative reverse transcription PCR and are designed within exon regions.

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