Answer:
There are a number of different methods employed including clot-based coagulation tests, chromogenic assays, immunological tests, and aggregation studies. Today automated machines are designed to be able to perform a number of different methodologies.
Explanation:
Answer:
Differences between Sympathetic and Parasympathetic
1. Anatomical: The location of preganglionic neurons of the autonomic ganglia and the extension of preganglionic and postganglionic fibers are different in these two systems;
2. Pharmacological: In the Sympathetic system we have the presence of Cholinergic fibers (Ach) and in the Parasympathetic system we have the presence of Noradrenergic fibers (NE);
3. Physiological: They act antagonistically, they rarely work harmoniously synergistically in coordinating visceral activity (balance)
All amino acids are structurally the same, in that they contain a central carbon atom, an amine group, a lone hydrogen at. Our DNA is contained in our chromosomes. The thing that is different about each of the 20 amino acids is the make-up of the R group
Answer:
In muscles contraction the correct order of the steps are: A (Nerve impulse reaches the muscle), B (Action potential travels down T-tubules), C (Calcium binds to troponin), D (Tropomyosin moves).
Explanation:
Skeletal muscle contractions are based on different physiological and biochemical phenomena that happen in every cell. These phenomena are due to stimulation produced by somatic motor neurons, which axons get in contact with muscle fibers through a neuromuscular synapse. In rest, attraction strengths between myosin and actin filaments are inhibited by the tropomyosin. When an action potential is originated in the central nervous system, it travels to the somatic motor neuron membrane: the muscle fiber, and activates the calcium channels releasing it in the neuron. Calcium makes vesicles to fuse with the membrane and release the neurotransmitter named acetylcholine (Ach) into the synaptic space in the juncture. Then, Ach binds to its receptors on the skeletal muscle fiber. This causes the ion channels to open, and positively charged sodium ions cross the membrane to get into the muscle fiber (sarcoplasm) and potassium get out. The difference in charges caused by the migration of sodium and potassium makes the muscle fiber membrane to become more positively charged (depolarized). The action potential caused by this depolarization enters the t-tubules depolarizing the inner portion of the muscle fiber. This activates calcium channels in the T tubules membrane, that make the calcium be released into the sarcolemma. At this point, tropomyosin is obstructing binding sites for myosin on the thin filament. When calcium binds to the troponin C, the troponin T alters the tropomyosin by moving it and then unblocks the binding sites. Myosin binds to the uncovered actin-binding sites, and while doing it ATP is transformed into ADP and inorganic phosphate. Z-bands are then pulled toward each other, thus shortening the sarcomere and the I-band, and producing muscle fiber contraction.
Covelent
<span>When electrons are transferred then ionic bond is formed and when electrons are shared then covalent bond is formed.</span>
