In the disease, Cystic Fibrosis (CF), a chloride channel (CF…

In the disease, Cystic Fibrosis (CF), a chloride channel (CFTR) is defective which results in reduced Cl− and water movement across the plasma membrane. In the lungs this is serious because mucus builds up leading to colonization by infectious bacteria. If you learn that the CFTR is a member of the family of ABC transporters, what might you conclude about the CFTR?

In your lab you are given the following components: 1) C16:0…

In your lab you are given the following components: 1) C16:0 palmitic acid            6) triacylglycerol 2) Sphingosine                        7) serine (an alcohol head group) 3) C18:1 Δ9 oleic acid            8) glucose 4) glycerol                               9) oligosaccharide (glucose-mannose-galactose-N-acetyl neuraminic acid) 5) cholesterol                         10) choline (an alcohol head group) What components are needed to form phosphatidylserine, a glycerophospholipid?

Do not answer this question until your exam has successfully…

Do not answer this question until your exam has successfully uploaded. To confirm that you have successfully submitted your assessment in Examplify and received the green upload screen answer the questions below and then click “Submit” to finish the Canvas quiz.  If you are unable to upload your exam in Examplify contact Dr. Ramey