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the answer is central nervous system
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<u>Answer:</u>
A is a DNA sequence that binds regulatory proteins that interact with promoter-bound proteins to activate transcription.
<u>Explanation:</u>
Background Knowledge:
DNA contains genes which is a particular segment of DNA. A gene usually has regulatory regions and a structural region.
Promoter: The regulatory region located to the 5 prime end of coding strand of the gene which is called as promoter that controls the binding RNA Polymerase during transcription.
The Terminator is the other regulatory region, located to the 3 prime end of coding strand of the gene. The terminator region causes RNA polymerase to stop transcription.
Structural region is the region present between the promoter and terminator.
Answer of the question is:
A is a DNA sequence that binds regulatory proteins that interact with promoter-bound proteins to activate transcription.
Answer: Sediment. Hope this helps :^)
Structures in plant leaves that open and close to maintain homeostasis are called stomata. This is where gases would diffuse in and out of the leaf.
Answer:
The stem cells possess two cardinal characteristics, that is, self-renewal and differentiation. The examples are embryonic stem cells and hematopoietic stem cells. The genetically determined immunodeficiency in a person is generally a result of the defective gene in the hematopoietic stem cells that produce red blood cells, white blood cells, and other components of blood.
The examples of genetically determined immunodeficiency diseases are SCID, X-linked Agammaglobulinemia, and others. The individual suffering from genetically determined immunodeficiency exhibits a defective gene in hematopoietic stem cells. There are two methods of treatment, that is, stem cell therapy and gene therapy.
The procedure of stem cell transplantation generally comprises HLA matching, in which the main step is to prevent graft rejection. It is succeeded by harvesting of hematopoietic stem cells from the HLA matched donor. The step of conditioning is performed to eradicate the recipient HSCs by radiotherapy and chemotherapy succeeded by the transfer of harvested donor HSCs to the patient or the recipient.
A person cannot receive his own stem cells as his or her each and every cell is defective in that specific gene accountable for the disease.
