Answer:
aorta
Explanation:
The aorta and its branches carries the blood to all the body's tissues.
"27 days, 7 hours, and 43 minutes for our Moon to complete one full orbit around Earth"
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>
The OCA2<span> gene's function is to provide inst</span><span>ructions in the process of making the p protein, hence the former name of the gene as P gene.An example of this process is the manufacturing in the body of melanin. The process of copying of OCA2 is called translation.</span>
Explanation:
A frameshift mutation is an insertion or deletion in a sequence of DNA which disrupts the way the code is read. It occurs when the codons undergo a disruption through the deletion or insertion of one or multiple nucleotides (given that the number removed or added are not multiples of 3) - this alters the open reading frame; the amino acids produced through translation simply occur in a different sequence.
Further Explanation:
During the process of cell division, spontaneous changes within the genome can arise. These mutations are errors occur when copies of the DNA within the cell are made; mutations may range from small changes called single nucleotide polymorphisms, to large scale deletions, and additions which span multiple genes. There are two types:
- somatic: these only occur within certain cells, and arise from environmental factors such as UV light
- hereditary: occur within germ cells of the parent and later the fertilized egg which forms a zygote; these are present within all cells of the new organism.
Learn more about mutations at brainly.com/question/4602376
Learn more about DNA and RNA at brainly.com/question/2416343?source=aid8411316
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