1)Chargaff's rules state that DNA from any cell of any organisms should have a 1:1 ratio of pyrimidine and purine bases and, more specifically, that the amount of guanine should be equal to cytosine and the amount of adenine should be equal to thymine. This pattern is found in both strands of the DNA.
2)DNA structure
DNA is made up of molecules called nucleotides. Each nucleotide contains a phosphate group, a sugar group and a nitrogen base. The four types of nitrogen bases are adenine (A), thymine (T), guanine (G) and cytosine (C). The order of these bases is what determines DNA's instructions, or genetic code.
3)A nucleotide consists of three things: A nitrogenous base, which can be either adenine, guanine, cytosine, or thymine (in the case of RNA, thymine is replaced by uracil). A five-carbon sugar, called deoxyribose because it is lacking an oxygen group on one of its carbons. One or more phosphate groups.
4)DNA replication is said to be semi-conservative because of this process of replication, where the resulting double helix is composed of both an old strand and a new strand. ... Semiconservative replication would produce two copies that each contained one of the original strands and one new strand.
5)The diagram has show in above.
6)complementary base pairing is necessary because the double helix shape would not be the same if not. Doubles would only pair with doubles and the singles to singles.
<u>HOPE</u><u> </u><u>THIS</u><u> </u><u>HELPS</u><u> </u><u>YOU</u><u>.</u>
Answer:
The return of blood to the heart is assisted by the action of the skeletal- muscle pump. As muscles move, they squeeze the veins running through them. Veins contain a series of one-way valves, and they are squeezed, blood is pushed through the valves, which then close to prevent backflow.
Answer:
Hemophilia is a x-linked recessive inherited bleeding disorder. in this disease blood does not clot properly due to the decreased level of blood clotting factor VIII (8) or factor IX (9).
In x-linked recessive condition, the disease is transmitted from father (affected male) to his daughter and mother (affected female) to her son and skip of generation getting affected is also occurs.
- there will be 50% chance of her (S.R.) each son to be affected with hemophilia.
Explanation:
Hemophilia is caused due to mutation of one gene which is responsible for the making of proteins of blood coagulation factor viii or ix. the affected person bleeds continuously from any injury and that can cause serious issues.
here,
grandfather of s.r is affected (xₐy) and grandmother is normal (xx) will produce
↓
s.r's mother who is a carrier (xₐx) [as xₐy and xx will produce 100% carrier xₐx daughter]
↓
s.r's mother is a carrier (xₐx) but her father is normal (xy) will produce,
↓
s.r who has 50% chance of being carrier (xₐx) and 50% chance of being normal (xx) [as she is the only child] and she has a normal (xy) partner, they will give,
↓
- if s.r is a carrier (xₐx) then one of her son will be affected (xₐy) [as xₐx and xy =xₐy]
- if s.r is normal (xx) then her son will be normal (xy) [as xx and xy will give xy]
here,<u> 50% chance of her son to be affected with hemophilia</u> [as S.R of being affected is more considerable].
The carbon that plants need for photosynthesis comes from (carbon dioxide gas in the atmosphere)
The pituitary gland is often called the "main gland" of the body, as it regulates many of the activities of the endocrine glands. ... HET (thyroid stimulating hormone) stimulates the thyroid gland to release T3 and T4 to stimulate metabolism in other cells of the body.
