The two ways by which we can detect that gene editing have occurred in the bacteria are;
A) WESTERN BLOT; Here,the gene that is edited will not be able to synthesize the protein.With this,if we do western against the already edited protein,no band will eventually appear in the western blot,and this indicates/confers that the gene have been edited.
B) PCR FOLLOWED BY SEQUENCING; IN PCR,there is amplification of the region with the use of flanking end primers that is edited.
However,mean primers will actually be used in a way that one primer is upstream to site of editing and the other primer to the downstream.
From this stage,the PCR product that is amplified will be sent for sequencing,and this sequency result will further confirm if the gene has been edited or not edited.
Restriction enzyme can also be used if the place where the gene has been edited is known.
If actually the gene has been edited,the nucleotide sequence will get changed.Having to choose such enzyme that cut only one's wide type wild type DNA but not actually gene that is edited,the result will further be compared inorder to confirm whether the gene has been edited or not.
The two experiments that can be done to detect gene editing including
Western blot and PCR(polymerase chain reaction)
DNA contain all the genetic properties of a cell and comprises of nucleotides with unique protein(amino) sequences. Western blot helps to detect specific protein through the sequences from a protein sample and helps to detect if editing took place.
Polymerase chain reaction(PCR) helps in the amplification of DNA which
helps to verify where editing took place if any.
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