Answer:
The human mitochondrial DNA (mtDNA) is a double-stranded, circular molecule of 16 569 bp and contains 37 genes coding for two rRNAs, 22 tRNAs and 13 polypeptides. The mtDNA-encoded polypeptides are all subunits of enzyme complexes of the oxidative phosphorylation system.
Explanation:
I have math language arts, gym, history/social studies, science, and spanish
Answer:
D Microwaves
Explanation:
It has an electromagnetic radiation with wavelengths ranging from about one meter to one millimeter; with frequencies between 300 MHz (1 m) and 300 GHz (1 mm)
Answer:
50%
Explanation:
Let's assume that the allele "T" gives the normal phenotype while the recessive allele "t" imparts the disease and is lethal in homozygous condition. The genotype of each of the two carrier parents would be "Tt". A cross between Tt and Tt would give the progeny in the following genotype ratio=
Tt x Tt= 1/4 TT: 1/2 Tt: 1/4 tt
Therefore, 1/2 or 50% progeny would be the carrier for the Tay-Sachs disease.
You may be referring to the nucleus. The nucleus controls the cell, and it contains chromosomes (DNA) genetic makeup. Hope I could help|!
