Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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- Clone number in this case is number 196 which is shown in the images. State whether a BamHI site has been re-created at the forward- and the reverse-end junctions of the human DNA with the plasmid vector band sizes are shown in one of the images. (0.5, 1, 2, 3, 4, 5, 6, 8, 10kb)arrow_forwardAfter Drosophila DNA has been treated with a restrictionenzyme, the fragments are inserted into plasmids and selected as clones in E. coli. With the use of this “shotgun”technique, every DNA sequence of Drosophila in a librarycan be recovered.a. How would you identify a clone that contains DNAencoding the protein actin, whose amino acid sequenceis known?b. How would you identify a clone encoding a specifictRNAarrow_forward24. Sickle-cell anemia arises from a mutation in the gene for the B chain of human hemoglobin. The change from GAG to GTG in the mutant that is located within the cleavage site for the restriction enzyme Mstll, which recognizes the target sequence CCTGAGG. These findings form the basis of a diagnostic test for the sickle-cell gene. Which answer best explains how this test should work? A) In combination with DNA polymerase, application of Mstll will produce long DNA strands with the normal gene but not the mutant gene. B) In combination with DNA polymerase, application of Mstll will produce long DNA strands with the mutant gene but not the normal gene. C) Treatment with Mstll produces DNA fragments from the normal gene but cannot cleave the normal gene. D) Treatment with Mstll produces DNA fragments from the normal gene but cannot cleave the mutant gene. E) Restriction enzymes are non-specific relative to the binding requirements for such a test. 25. The restriction enzymes Kpnl and…arrow_forward
- a.) wanting to clone gene Z into pVector, the gene is amplified by PCR and restriction sites are added to the flanking ends. without realizing that the antibotic resistant gen )tetR) had a Sal1 site, you decide to add EcoR1 and Sal1 recofnition sequencen into the 12-nucleotide primers. Write the sequence of the 2 primers, noting the 5' and 3' ends?arrow_forwardSuppose that you want to assay reverse transcriptase activity. If polyriboadenylate is the template in the assay, what should you use as the primer? Which radioactive nucleotide should you use to follow chain elongation?arrow_forwardCan you help solve this problem?arrow_forward
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