Answer:
here is the order
Genetics
Allele
Hybrid then law of independent assortment
Law of segregation
Answer: The theory of cheek cells is used for the identification of cheek cells.
Explanation:
The cells of cheek do not have cell wall. They have a cell membrane which allows on certain molecules to pass through it. The nucleus is located centrally in the cheek cells and it stores the DNA. It can be stained with the help of the methylene blue reagent. It appears blue in color which can be observed under the microscope. The cheek cells can be isolated from the buccal cavity by using cotton buds and cotton swabs can help in isolating the cells.
Answer:
The cell interior would experience higher than normal Na+ concentrations and lower than normal K+ concentrations.
Explanation:
Na+/K+ ATPase exists in two forms: Its phosphorylated form has a high affinity for K+ and low affinity for Na+. ATP hydrolysis and phosphorylation of the Na+/K+ pump favor the release of Na+ outside the cell and binding of K+ ions from the outside of the cell. Dephosphorylation of the pump increases its affinity for Na+ and reduces that for K+ ions resulting in the release of K+ ions inside the cells and binding to the Na+ from the cells.
The presence of ATP analog would not allow the pump to obtain its phosphorylated form. Therefore, Na+ ions would not be released outside the cells. This would increase the Na+ concentration inside the cell above the normal. Similarly, the pump would not be able to pick the K+ from the outside of the cell resulting in reduced cellular K+ concentration below the normal range.
The epiglottis is a flap in the back of your tongue that prevents food from entering the larynx. When your mouth is closed, the epiglottis is in place and blocks the larynx opening. If your mouth is open, the flap lifts and the larynx is no longer blocked so you can breathe. This is why it's important to not chew with your mouth open... if you do, then food can go down the larynx by mistake.
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].
