All changes saved 1. Gia, the charge nurse on a busy recovery floor, notices that someone keeps forgetting to reprogram the pump when setting up a
new IV medication. The patient then receives the medication at whatever rate the machine was programed to prior. So far, nothing
dangerous has happened but Gia must make sure this error does not continue to happen. She looks over the records and manages
to narrow it down to one nurse: Hae. Hae should know how important this is, but Gia Imagines it is just carelessness. What would be
the BEST way for Gia to handle this issue?
O
Call a team meeting and tell everyone about the mistake Hae has been making.
Assign another nurse to go behind Hae and double check that the machine is correct.
Speak to Hae one on one to make sure she understands how to reprogram the machine.
O
Put a notice on the nurses' station in large letters reminding everyone to reprogram.

Mouse liver cells were homogenized and the homogenate subjected to equilibrium density-gradient centrifugation with sucrose gradients. fractions obtained from these gradients were assayed for marker molecules (i.e., molecules that are limited to specific organelles). the results of these assays are shown in the figure. the marker molecules have the following functions: cytochrome oxidase is an enzyme involved in the process by which atp is formed in the complete aerobic degradation of glucose or fatty acids; ribosomal rna forms part of the protein-synthesizing ribosomes; catalase catalyzes decomposition of hydrogen peroxide; acid phosphatase hydrolysis monophosphoric esters at acid ph; cytidylyltransferase is involved in phospholipid biosynthesis; and amino acid permease aids in transport of amino acids across membranes. a) name the marker molecule and give the number of the fraction that is most enriched for each of the following cell components: lysosomes; peroxisomes; mitochondria; plasma membrane; rough endoplasmic reticulum; smooth endoplasmic reticulum.

Which is an example of a decomposer? a. bear b.algae c.grass d.bacteria d bacteria

Select the correct answer. tay-sachs disease is caused by a mutation in the hexa gene located on chromosome 15. tay-sachs follows an autosomal recessive pattern of inheritance. with the of the diagram, identify which of the offspring will be an unaffected carrier. a diagram showing the genes of parents who are carriers of tay-sachs disease a. a, b, and c b. b and c c. a and d d. a e. d