GENETIC ANALYSIS: AN INTEG. APP. W/MAS
GENETIC ANALYSIS: AN INTEG. APP. W/MAS
2nd Edition
ISBN: 9781323142790
Author: Sanders
Publisher: Pearson Custom Publishing
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Chapter 6, Problem 16P

Suppose you have an rII lysis mutant that maps to segment A2h2 . Use the Series I and Series II deletion mutants identified in the problem above, and fill out the “results” columns with the “+” and “-” designations expected for the A2h2 mutant. Chapter 6, Problem 16P, 16. Suppose you have an lysis mutant that maps to segment. Use the Seriesand Series deletion mutants

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When human hemoglobin undergoes a mutation, the mutant protein usually does not replace all of the normal HbA in the red blood cells or erythrocytes of the individual. The erythro- cytes contain mixtures of varying amounts of both HbA and the mutant protein depending on the mutation and the individual. Hb Yakima is a mutant human Hb with an Asp-(B99)His mutation. The diagram on the right shows that Hb Yakima was separated by DEAE-cellulose chromatography from HbA with a 0 – 0.1 M linear gradient of NaCl buffered to pH 8.3. Why is chromatog- raphy carried out at pH 8.3? If the isoelectric point of HbA is 6.85, what is the change in total charge caused by the mutation?How does the change in charge explain the chromatography elution profile of the Hb Yakima/HbA mixture? 1,5 -Hb-A Hb -Yakima 1.0 0.5- 20 40 60 80 00 Fraction number O.D578 nm
For each of the E. coli strains containing the lacoperon alleles listed, indicate whether the strain isinducible, constitutive, or unable to expressβ-galactosidase and permease.a. I+ o+ Z− Y+/ I+ ocZ+ Y+b. I+ o+ Z+ Y+/ I− ocZ+ Y−c. I+ o+ Z− Y+/ I− ocZ+ Y−d. I−P− o+ Z+ Y−/ I+ P+ ocZ− Y+e. Iso+ Z+ Y+/ I− o+ Z+ Y−
Genomic DNA from a family where sickle-cell disease is known to be hereditary, is digested with the restriction enzyme MstII and run in a Southern Blot. The blot is hybridised with two different 0.6 kb probes, both probes (indicated in red in the diagram below) are specific for the β-globin gene (indicated as grey arrow on the diagram below). The normal wild-type βA allele contains an MstII restriction site indicated with the asterisk (*) in the diagram below; in the mutated sickle-cell βS allele this restriction site has been lost. What size bands would you expect to see on the Southern blots using probe 1 and probe 2 for an individual with sickle cell disease (have 2 βS alleles)?     Probe 1 Probe 2 (a) 0.6kb 0.6kb and 1.2kb (b) 0.6kb and 1.8kb 0.6kb, 1.2kb and 1.8kb (c) 1.2kb 0.6kb (d) 1.8kb 1.8kb   a. (a)   b. (b)   c. (c)   d. (d)

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GENETIC ANALYSIS: AN INTEG. APP. W/MAS

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