Answer:
fatty acid and lipids
Explanation:
buttons always drop down this is easy kids
The answer is <span>Anaphase I separates homologous chromosomes and anaphase II separates sister chromatids into daughter cells.</span>
Meiosis is a cell division which results in the reduction of chromosome number by half - from diploid to haploid - in daughter cells. It consists of meiosis I and meiosis II. Meiosis I produces two haploid cells. Meiosis II is analogous to mitosis, so in total, meiosis results in four haploid cells. So, in meiosis, there are two anaphases - the anaphase I in meiosis I and the anaphase II in meiosis II.
<span>In anaphase I, the sister chromatids separate from each other to the opposite sides of the cells. In meiosis I there are 46 chromosomes in duplicate, which are present as pairs of sister chromatids. In anaphase of meiosis II, since the cell is haploid, there are 23 chromosomes in duplicate, which are present as sister chromatids.</span>
Answer:
The genotype for each of the parents must be
parent 1 : Gg
parent 2 : Gg
Explanation:
Please note that a dominant trait is a trait that is expressed phenotypically in a heterozygous state, while a recessive trait is a trait that can only be expressed in a homozygous state.
Now, since gray face (G) for Oompa Loompas is dominant, and orange face (g) is recessive, for an offspring to be orange faced, it means that the genotype of the offspring must be 'gg'. Also, since both parent contribute an allele in the pair of alleles in the offspring, both parents must have the recessive (g) in their genotype. Moreover, we are told that both parents are gray-faced, meaning that their genotypes were 'Gg' and 'Gg'. To confirm, let me do the cross
G g
G GG Gg
g Gg gg
from the cross above, we find out that out of 4 offspring, 3 were gray face (GG, Gg ) while one was orange face (gg).
People with two copies of the sickle cell gene have the disease. People who carry only one copy of the sickle cell gene do not have the disease, but may pass the gene on to their children. Abnormal hemoglobin, called hemoglobin S, causes sickle cell disease (SCD). The problem in hemoglobin S is caused by a small defect in the gene that directs the production of the beta globin part of hemoglobin. This small defect in the beta globin gene causes a problem in the beta globin part of hemoglobin, changing the way that hemoglobin works.
Carbon dioxide is the compound in photosynthesis, I'm pretty sure
