Answer:
The earth moves two ways. It spins and it moves around the sun. The spinning of the earth is called rotation. It takes the earth abut 24 hours, or one day, to make one complete rotation.
Explanation:
The earth moves two ways. It spins and it moves around the sun. The spinning of the earth is called rotation. It takes the earth abut 24 hours, or one day, to make one complete rotation.
Answer:
chromosomes
Explanation:
chromosomes which consist of genes which consist of DNA can pass on traits from parent to child.
it basically works by depending on the gender of the child it can inherit certain traits from its parents
so say the hemophilia is an XX being from the mom and to get the mutation you would need the X that has the mutation and either an X or Y from the dad.
I dont know if hemophilia affects X or Y but that is how the mutation would be passed on.
Answer:
Plasmolysis
Explanation:
In the image 1 the cell is having sufficient quantity of water leading to a turgid cell.
The image 1 plant cell is in a dilute solution in which water enters into cell from external medium.
The image 2 plant cell is exposed to a solution which is high concentrated solution.
Due to this high concentrated solution the water present in the cell is send out by exosmosis.
Due to loss of water from plant cells the protoplasm in plant cell shrinks in which cell membrane gets separated from cell wall.
This shrinkage of protoplasm by loss of water is called plasmolysis.
The answer is; Benedict’s reagent
It is used to test for reducing sugars. In presence of these sugars, the reagent, that is blue in color, turns different shaded of red (to brick red), depending on the amount of reducing sugars in the solution. It is important to note that the solution has to be heated.
With the sequence of the gene-coding regions of the human genome in hand and the development of newer sequencing methods, scientists are able to
1. develop new forensic tests that can help in the identification of the convict.
2. diagnose genetic diseases before their onset.
3. develop customised medicines based on the genetic profile of the patient.
4. therapeutically target the cancer causing genes (oncogenes) in the patients.
5. understand the inheritance of genes especially the rare mutations in a population.
