Recombinant DNA Technology Which of the following is correct in terms of determination of location of genetic traits? None of these Known protein coding sequences are too far apart to allow linkage determination for most new genes Restriction sites allow DNAs to be digested Protein-coding genes are always associated with a restriction pattern None of these Known protein coding sequences are too far apart to allow linkage determination for most new genes Restriction sites allow DNAs to be digested Protein-coding genes are always associated with a restriction pattern ANSWER DOWNLOAD EXAMIANS APP
Recombinant DNA Technology Which type of restriction enzymes do not usually require ATP? Type IV Type I Type II Type III Type IV Type I Type II Type III ANSWER DOWNLOAD EXAMIANS APP
Recombinant DNA Technology In order to insert a foreign gene into a plasmid, both must __________ have identical DNA sequences be cut by the same restriction enzyme be of the same length originate from the same type of cell have identical DNA sequences be cut by the same restriction enzyme be of the same length originate from the same type of cell ANSWER DOWNLOAD EXAMIANS APP
Recombinant DNA Technology The order for the construction of a cDNA fragment from mRNA is to bind oligo-dT, treat with reverse transcriptase, digest with RNase, add G residues to the 3' end, bind oligo-dC, treat with DNA polymerase bind oligo-dC, treat with reverse transcriptase, digest with RNase, add G residues to the 3' end, bind oligo-dT and treat with DNA polymerase digest with RNase, add G residues to the 3' end, treat with reverse transcriptase, add G residues to the 3' end and treat with DNA polymerase treat with reverse transcriptase, digest with RNase, add G residues to the 3' end, bind oligo-dC, treat with DNA polymerase and bind oligo-dT bind oligo-dT, treat with reverse transcriptase, digest with RNase, add G residues to the 3' end, bind oligo-dC, treat with DNA polymerase bind oligo-dC, treat with reverse transcriptase, digest with RNase, add G residues to the 3' end, bind oligo-dT and treat with DNA polymerase digest with RNase, add G residues to the 3' end, treat with reverse transcriptase, add G residues to the 3' end and treat with DNA polymerase treat with reverse transcriptase, digest with RNase, add G residues to the 3' end, bind oligo-dC, treat with DNA polymerase and bind oligo-dT ANSWER DOWNLOAD EXAMIANS APP
Recombinant DNA Technology In gel electrophoresis, DNA molecules migrate from __________ to __________ ends of the gel. negative ... positive positive to negative basic ... acidic long ... short negative ... positive positive to negative basic ... acidic long ... short ANSWER DOWNLOAD EXAMIANS APP
Recombinant DNA Technology Which of the following techniques can be used to determine the defective gene and for developing cancer? Eastern blot Southern blot Northern blot Western blot Eastern blot Southern blot Northern blot Western blot ANSWER DOWNLOAD EXAMIANS APP
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