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My DNA insert size is 746bp. I have designed the primers with the EcoR1 and Sal1 enzyme sites at 5'.
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I used initial denaturation at 95 for 10 min followed by 94 for 45 sec. Temperature gradient for annealing temp from 62 to 73 at 1 min. Extension time : 68 for 6 min and further 68 for 10 min....
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I just narrowed it down to the specific exon of gene of my interest but I am not sure how to make multiple gRNAs for the same gene target? What points should be kept in mind while designing the gRNAs?
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I am new to this and need to order for my experiment work. Please elaborate from the basics
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