Karyotypes can be studied to determine an organism’s chromosomal makeup and to detect genetic defects. Down syndrome is a genetic disorder that is also called trisomy 21. What would trisomy 21 look like in a karyotype?

The dna in a cell’s nucleus encodes proteins that are eventually targeted to every membrane and compartment in the cell, as well as proteins that are targeted for secretion from the cell. for example, consider these two proteins: phosphofructokinase (pfk) is an enzyme that functions in the cytoplasm during glycolysis. insulin, a protein that regulates blood sugar levels, is secreted from specialized pancreatic cells. assume that you can track the cellular locations of these two proteins from the time that translation is complete until the proteins reach their final destinations.for each protein, identify its targeting pathway: the sequence of cellular locations in which the protein is found from when translation is complete until it reaches its final (functional) destination. (note that if an organelle is listed in a pathway, the location implied is inside the organelle, not in the membrane that surrounds the organelle.)

There is a liquid capsule inside a cup full of liquid. the cup full of liquid has salt in it and the liquid capsule has no salt in it. in which direction will the solvent flow? a. the salt does not have to move b. from the capsule to the larger cup c. equally between the capsule and the cup d. from the larger cup to the capsule

Suppose a point mutation, such as a change from an adenine to a guanine, occurs in the genome of a human sperm cell. the mutation could occur in any region of a gene. the effect of the mutation on the phenotype of the offspring will be determined by where the mutation occurs and its effect on the final gene product. in which of the following scenarios could the mutation alter the phenotype of the offspring? select all of the scenarios that apply the mutation occurs in the promoter and affects the rate of gene transcription. the mutation results in a new, dominant allele the mutation occurs in a portion of an intron not responsible for exon splicing the mutation occurs in a gene that controls development and alters differentiation of a cell type during development. the mutation occurs in a codon and alters the function of the final protein e mutation occurs in a codon, and the amino acid sequence of the final protein is unchanged.