Answer:
Lysosomes.
Explanation:
HEXA (Hexosaminidase A) is the functional enzyme and encoded by the HEXA gene. The main function of this enzyme is the hydroxylation of the gangliosides.
The mutation in this gene leads to the lysosomal storage disease. The GM2 starts accumulating in the lysosomes and causes Tay Sach's disease. This is a genetic disorder that leads to the breakdown of the cells of the spinal cord and the brain.
Thus, the answer is lysosomes.
Answer:
sporopollenin
While the exine is composed of sporopollenin, a complex and highly resistant biopolymer containing fatty acids, phenylpropanoids, phenolics and carotenoids, the intine is largely composed of pectin and cellulose.
Explanation:
Its the epidermis because it is subdivided into two layers.
Answer:
Chromosome 17 is made of over million (80) base pairs.
Approximately how many genes are found on chromosome 17?
1600
Explanation:
took on edge2020 and got it right
hope this helps :)
The graph that is represented is a line graph.