Yes. You could do this by adding solvents to break down any cell walls, centrifuge to separate the DNA, if you haven't got much then upscale with PCR, gel electrophoresis could be used to detect the DNA, and Sanger sequencing to find the sequence.
Answer:
False
Explanation:
Introns need to be removed precisely because the reading frame will be shifted if removed even single nucleotide too many or leaving an intronic nucleotide in the spliced mRNA .
Extra amino acids will be inserted if large pieces of introns are left in the mature messenger RNA.
In both cases, aberrant protien will be produced if the RNA splicing is not precise, hence they are needed to be removed by precision.
One affects radicle (root) growth while the other affects plumule shoot growth.
