Cl 1- has 17 protons and 18 electrons
K 1+ has 19 protons and 18 electrons
S 2- has 16 protons and 18 electrons
Sr 2+ has 38 protons and 36 electrons
Al 3+ has 13 protons and 10 electrons
P 3- has 15 protons and 18 electrons
Si 4- has 14 protons and 18 electrons
56+/54- has a charge of +2
87+/86- has a charge of +1
84+/86- has a charge of -2
50+/46- has a charge of +4
32+/36- has a charge of -4
55+/54- has a charge of +1
12+/10- has a charge of +2
C. Stationary front
Hope this helped !
The segments of the DNA that are transcribed into mRNA and are used to produce amino acids are called EXONS. This segments are coding regions. In the transcription process, the non-coding regions are removed and the only segments that remain are the coding regions. The exons are used to produce amino acids.
so you wont get hurt while doing something
What is Sickle cell anemia?
Sickle cell is an autosomal recessive trait of humans that arises through mutation in normal gene. The gene for this trait is found in recessive form and you need two copies of the gene - one from father and one from mother- to have the trait expressed. If the trait is expressed it causes a disease called sickle cell anemia.
People with the sickle cell anemia disease have red blood cells of crescent or sickle shape. The red blood cells of this shape can cause many complications in body. They get stuck in blood vessels and cause pain. They also die quickly and make a person anemic (pale).
Probability to have a child with sickle cell anemia:
If a mother is normal but a father is carrier for the trait, then the situation will be as:
Here N indicate normal allele, S indicate allele for sickle cell anemia.
Mother ˣ Father
NN NS
Gametes: N N N S
Offspring: NN NS NN NS
50% : Normal
50% : Carrier
0% : Sickle cell anemia
It means that 50 % kids will be normal and 50% will be carrier for the trait and none of the offspring will have disease Sickle cell anemia.
However, those who are carriers can carry the disease to the next offspring if they are married to a carrier or a person with sickle cell anemia.
