You are interested in exocytosis and endocytosis in a line of cultured liver cells that secrete albumin and take up transferrin. To distinguish between these events, you tag transferrin with colloidal gold and prepare ferritin labeled antibodies that are specific for albumin. You add the tagged transferrin to the cell culture medium, and then after a few minutes you fix the cells, prepare thin sections, and react them with ferritin-labeled antibodies against albumin. Colloidal gold and ferritin are both electron-dense and therefore readily visible when viewed by electron microscopy. Additionally, they can be easily distinguished from one another on the basis of size. A) Will this experiment allow you to identify vesicles in the exocytic and endocytic pathways?
B) Not all the gold labeled vesicles are clathrin-coated. Explain this result.

the transfer for conduction is the heat transfering from the liquid to the spoon

the transfer for convection is the heat rising from the liquid to the air

the transfer for radiation is the heat going through the sides of the cup and to the air

at least that is what i would do

an individual’s sex (i.e., whether they are a male or female) is determined by the sex chromosomes. most people have two sex chromosomes, one that is inherited from their mother and one that is inherited from their father. typically, females have two x chromosomes (xx) and males have one x chromosome and one y chromosome (xy). conditions caused by changes (“mutations”) in genes located on the x chromosome are considered x-linked.

x-linked recessive inheritance

most x-linked conditions are recessive. this means that in a person with two x chromosomes (most females), both copies of a gene (i.e., one on each x chromosome) must have a change or mutation whereas in a person with one x chromosome (most males), only one copy of a gene must have a mutation. a female with a mutation in one copy of a gene on the x chromosome is said to be a “carrier” for an x-linked condition. a male with a mutation in a gene on the x chromosome is typically affected with the condition. because females have two copies of the x chromosome and males have only one x chromosome, x-linked recessive diseases are more common among males than females. however, x-linked recessive diseases can occur in both males and females.

for x-linked recessive disorders, an unaffected carrier mother who has a mutation in a gene on the x chromosome can transmit either the x chromosome with this mutation or a “normal” x chromosome to her children. if the father is unaffected, none of her daughters will be affected and all of her daughters will be unaffected—since they will inherit at least one normal x chromosome from their father. however, each daughter will have a 50% chance of being an unaffected carrier like her mother and a 50% chance of both x chromosomes being normal.