The true statement of chemical bonds is covalent bonds share electrons between two atoms.
In conclusion, covalent bonds share electrons between two atoms.
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Explanation:
They are two types of simple columnar ephitelia. Simple columnar ephitelia with microvilli secrete digestive enzymes and absorb digested food.
The simple ephitelia with cilia aid in the movement of mucus and reproducitve cells.
Answer: They are examples of Simple Columnar Epithelia.
Explanation:
For example:In female reproductive organs, the epithelium lines together with the fallopian tubes, endometrium and the inner part of the cervix (endocervix)
B. Oceanic crust is denser than continental crust.
C. Oceanic crust is less dense than continental crust.
D. Oceanic crust is older than continental crust.
Answer:
B.) Oceanic crust is denser than continental crust.
Explanation:
Oceanic crust is denser, so it is subducted under the continental crust. The less dense magma then rises up through the continental crust, then it's further increasing the size of the continental crust and then maintaining it's lower density than the oceanic crust, which then causes subduction.
I hope this helped. I am sorry if you get this wrong.
Answer:
B.) Oceanic crust is denser than continental crust.
Explanation:
I just did it and got it right :)
b. False
The answer is true. Addiction is a chronic, often relapsing brain disease that causes over time challenge an addicted person's self-control and hampers his or her personality. Drugs are chemicals that tap into the brain’s communication system and disrupt the way nerve.
Answer:
Mixed inhibition refers to the combination of two reversible types of enzyme inhibition, competitive inhibition and non-competitive inhibition. The term mixed is used when the inhibitor can bind both the free enzyme and the enzyme-substrate complex. In mixed inhibition the inhibitor is in a different place from the active site where the substrate is found.
Mathematically, mixed inhibition occurs when both alpha and alpha-prime factors (introduced in the Michaelis-Menten equation representing competitive and non-competitive inhibition respectively) are present (they are larger than unity).
In a special case of mixed inhibition, the alpha and alpha-prime factors are the same, then non-competitive inhibition occurs.
With this type of inhibition Km depends on the affinity of the inhibitor to join E or ES and Vmax decreases.
Enzymatic inhibitors are molecules that bind enzymes and decrease their activity. Since blocking an enzyme can kill a pathogen or correct a metabolic imbalance, many medications act as enzyme inhibitors. They are also used as herbicides and pesticides. However, not all molecules that bind to enzymes are inhibitors; Enzymatic activators bind to enzymes and increase their activity.
The binding of an inhibitor can prevent the substrate from entering the active site of the enzyme and / or hinder the enzyme from catalyzing its corresponding reaction. The inhibitor binding may be reversible or irreversible. Normally, irreversible inhibitors react with the enzyme covalently and modify their chemical structure to the level of essential residues necessary for enzymatic activity. In contrast, reversible inhibitors bind to the enzyme in a non-covalent manner, resulting in different types of inhibitions, determined whether the inhibitor binds to the enzyme, the enzyme-substrate complex or both.
Many medications are enzymatic inhibitors, so their discovery and improvement is an active field of research in biochemistry and pharmacology. The validity of a medicinal enzyme inhibitor is usually determined by its specificity (its inability to bind to other proteins) and its potency (its dissociation constant, which indicates the concentration necessary to inhibit an enzyme). A high specificity and potency ensures that the medication will have few side effects and therefore a low toxicity.