Answer:
Voltage-gated Ca2+ channels
Explanation:
Modulation of Ca+2 channel Epinephrine also causes an increase in cAMP that stimulates PKA that is protein kinase A, which in turn phosphorylates the voltage-gated Ca+2 channel that is the L channel. This phosphorylation results in a protein conformational change that enchances the channels activity.
Answer:
Translation
Explanation:
The translation is the process during which the nucleotide sequence of the mRNA is read in the form of genetic codes. The nucleotide sequence of mRNA is complementary to the template DNA strand. According to the sequence of the nucleotides in the mRNA, the amino acids are added in a specific order to make the polypeptide chains. The process occurs on ribosomes. The ribosomes move along the mRNA to read its sequence and the tRNA brings are amino acids to be added to the polypeptide chains.
Answer:
Gated ion-channels
Explanation:
These ion channels are protein molecules that act as a passageway which span across the cell membrane allowing the movement of ions from one side of the membrane to the other. They possess the ability to open and close in response to either chemical or mechanical signals.They possess a fluidic pore, which becomes available to ions after a conformational change in the protein structure has been activated causing the ion channel to open. Based on the stimulus to which they respond, ion channels are divided into three groups: voltage-gated, ligand-gated and mechano-sensitive ion channels. Channels responding to electrical (voltage-dependent ion channels), mechanical, or chemical (ligand-gated ion channels) stimuli open and allow rapid ion movement into or out of the cell, and this movement creates an electrical signals.
Answer:
Cross-pollination.............
Answer: His genes contain a mutation that prevents red blood cells from proper functioning.
Explanation:
Hereditary anaemia is a type of disorder that are genetically transmitted to the offsprings by the parents . These type of anaemia are inherited from the parent including sickle cell anaemia.
The offsprings inherent Gene mutation that cause abnormalitiies. They inherit abnormal haemoglobin that can reduce the life span of red blood cells thereby affecting their proper functioning of carrying oxygen in the blood, leading to anaemia.
