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.
Explanation:
Body cells make up the body of any multicellular organism. A body cell contains a complete number of chromosomes and is called a diploid cell while a gamete contains only half the number of chromosomes of its parent cell, and it is called a haploid cell.
Hope it's R8
Step 1: Copy of one side of DNA strand is made (called mRNA, messenger RNA)
step 2: mRNA moves to cytoplasm, then ribosome
step 3: mRNA goes through ribosome 3 bases at a time
step 4: transfer RNA (tRNA) matches up with the open DNA bases
step 5: tRNA releases the amino acid at the top, which joins the chain of amino acids being produced
Answer:
adaptations; anything ( food storage, movement, thermoregulation)
Explanation:
Characteristics that animals inherit to help them survive in their environment are called adaptations.
Along with water conservation, animals also have unique characteristics for food storage, movement, etc; (anything that is a regulatory thing seems to fit here).
Warm and dry is the answer
