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Ethylene synthesis in plants is tightly regulated and post transcriptionally controlled. Explain. Design an experiment to show that proteasome degradation is involved?
Assume your patient is receiving NPH insulin in the morning and evening The 5 p.m. insulin check is high and is to be treated with regular insulin.
The calculation of interaural time difference (ITD) is often modeled as a cross correlation. Re-write the cross-correlation equation in terms of ITD.
What strategies do other organisms have that allow them to live in environments that are hypertonic to their cytoplasm. What is the pattern in data from Seeley's field experiment.
If the horticulturist breeding gardenias succeeds in having a single plant with a particularly advantageous set of traits, which would be her most probable and efficient route to establishing a line of such plants.
Spiny species of diatoms are found both in warm subtropical waters in addition to in colder areas. Since warm water is less dense than cold water, would you predict any differences between the spines of warm-water and cold-water individuals? Why.
Carbon fixation requires the expenditure of ATP molecules which is generated by A. formation of glucose during the Calvin cycle B. replenishment of chlorophyll C. ETS.
A semipermeable membrane separates two aqueous solutions at thirty degrees C. For each of the following cases, name the solution into which a net flow of water.
The expression and purification of rGFP started with the increase of the bacterial culture and ended with elution of rGFP off the Ni+2 agarose coloumn.
The maltose transporter maltoporin spans the outer membrane of E. coli. It is comprised of 18 successive antiparallel Beta - strands arranged like the staves of a barrel to create a channel through the membrane.
Assume you ingest 20 cells of Salmonella typhimurium in a chicken taco. Some of the bacteria are killed as they pass through the stomach but ten viable cells survive and reach the intestine.
Assume your lab partner leaves in the middle of making a 50mM NaCl solution. You know that they transferred 6mls of a 250mM stock solution into a beaker,
Sanger-based sequencing needs very specific DNA and primer concentrations for optimal performance. For template DNA like plasmids, DNA needs to be at a concentration of 50ng/ul in 10 ul.
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