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1. What proteins are required to move copies of DNA to opposite sides of the dividing cell ?
2. FtsI proteins catalyze what reaction ?
3. What happens to the peptidoglycan precursor during transpeptidation ?
4. With no translational machinery ( ribosomes, tRNAs) encoded by the virus, how does the virus make its proteins ?
5. What is the origin of all antibiotics ?
6. All enzymes secreted by the small intestine?
7. What are all the different enzymes secreted in the small intestine and its function?
The information presented in Problem seven are analyzed using multiple linear regression analysis and the models are shown here. In the models, the data are coded as 1= new.
Discuss two of the non-covalent forces that stabilize tertiary structure in proteins that are affected when the pH is changed.
According to the function of the genes, are they involved in a specific cellular process? If so what process? Does this make sense for gene expression in cancer?
You are a technician in a hospital laboratory. Three members of one family, two kids (ages 4 & 8) and their mother, have presented at the local Emergency Room at 5:00PM with symptoms of double vision,
The chemical equation FeS --> Fe + S is anexample of this kind of reaction. Potential energy can be illustrated by which ofthe following examples?
Determine what features distinguish association cortices from sensory and motor cortices? Consider thalamic input and corticocortical connections.
If you transform bacteria with the plasmid library made in part b above, divide the transformatnts into 20 aliquots and find one has the insert of interest, now how many clones do you need to screen.
q. in the yawncat a rare hypothetical animal the dominant allele r causes solid tail colour and the recessive allele r
During gym class Sally noticed that her friend Melissa always ran faster than her. Sally knew that they exercised equally, so she wondered what could cause Melissa to run so fast.
What is the effect of varying the primary stain and counterstain in acid-fast staining?
q1. you preformed cot analysis using genomic dna samples obtained from a 2 year-old child and a 76 year-old individual.
Why do you think that some of the cells in certain flasks looked healthier than other ones? What is present or absent in the growth media of the different flasks that can make a difference?
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