Learning Task 1: Let's Compare. Directions:
1. Study carefully the sequence of the amino acid.
2. Given are the sequence of amino acids in the cytochrome C of the human, chimpanzee, gorilla,
Rhesus monkey, horse, and kangaroo.
Note: Cytochrome C is a respiratory enzyme located inside the mitochondria.
3. Identify the differences using the amino acid sequence of human as
reference. Refer to table 1 for your answer.
4. Supply the missing amino acid sequence of chimpanzee, gorilla, Rhesus
monkey, horse, and kangaroo to complete Tables 2, 3, and 4 in a separate sheet of paper.
5. Complete Table 5 to show the number of amino acid differences and the position which they vary,​

answer by yourhope:

hi! : )

in which structure in the nucleus are ribosomes made?

b) nucleolus!

: )

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.

the correct answer is option d.

an appositive is a noun, noun phrase or noun clause which follows another noun or noun phrase in order to describe it or name it another way. they are usually used between commas, brackets or dashes.

the example sentence with the correct use of commas is the following:

her uncle, the man over there in the red shirt, owns the hardware store in town.