Recombinant DNA Technology Under which of the following conditions would population gene frequencies remain the same? Small population size Active migration between groups Random mating Selection for homozygotes Small population size Active migration between groups Random mating Selection for homozygotes ANSWER DOWNLOAD EXAMIANS APP
Recombinant DNA Technology Some genetic diseases cannot be diagnosed by changes in restriction sites. Some of these can be detected by allele-specific oligonucleotide probes. These are PCR-amplified variable numbers of tandem repeats (VNTRs) mutagenized copies of a gene short sequences that will hybridize only to a specific base sequence copies of the gene with an altered sequence so that a restriction site is inserted PCR-amplified variable numbers of tandem repeats (VNTRs) mutagenized copies of a gene short sequences that will hybridize only to a specific base sequence copies of the gene with an altered sequence so that a restriction site is inserted ANSWER DOWNLOAD EXAMIANS APP
Recombinant DNA Technology Which of these genes codes for a protein that plays a role in growth? SCLC6A4 KRTHA1 GH1 DCP1 SCLC6A4 KRTHA1 GH1 DCP1 ANSWER DOWNLOAD EXAMIANS APP
Recombinant DNA Technology The unpaired nucleotides produced by the action of restriction enzymes are referred to have sticky ends restriction fragments single strands ligases sticky ends restriction fragments single strands ligases ANSWER DOWNLOAD EXAMIANS APP
Recombinant DNA Technology The order for the construction of a cDNA fragment from mRNA is to 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 bind oligo-dT, treat with reverse transcriptase, digest with RNase, add G residues to the 3' end, bind oligo-dC, treat with DNA polymerase ANSWER DOWNLOAD EXAMIANS APP
Recombinant DNA Technology Which type of restriction enzymes do not usually require ATP? Type IV Type I Type III Type II Type IV Type I Type III Type II ANSWER DOWNLOAD EXAMIANS APP
EXAMIANS