You denature the above molecule (i. e. separate the double helix into two single-stranded dna molecules), allow the primer 5’gggagtcgaat 3’ to hybridize (hydrogen bond) with one of the two strands, and add the resulting molecule and dna polymerase to your assay system. write the complete sequence of the new strand of dna (excluding the primer and template sequence) that will be synthesized in the above reaction. be sure to label the 5’ and 3’ ends of this sequence.