Our lab has been making RNA libraries using a TruSeq RNA kit v2. Right now we have enough of all of the kit reagents for our libraries, except for the second strand master mix.
Has anyone tried substituting other second strand enzyme mix in this protocol? Or using a different protocol from the one in the kit to convert RNA to cDNA before proceeding with library production?
Has anyone tried substituting other second strand enzyme mix in this protocol? Or using a different protocol from the one in the kit to convert RNA to cDNA before proceeding with library production?
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