Answer:
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Explanation:
Nucleotides are A & T and G&C you see in DNA and in RNA T is Replaced by U. The reason they must be balanced between G&C and T&A is because G has to bond with A in DNA and G with C so if there is more G than C that means there is mismatches between the DNA nucleotides same thing for A and T. In RNA you follow the same rule. If we have lets say 27% of our DNA as A we have to have 27% as T leaving 23% as C and 23% as G. If there was lets say 29% T while one 27% A then there was a error in DNA replication and could lead to errors in RNA synthesis if not corrected
The answer to this is Lipids, nucleic acids, proteins, glycerol and fatty acids.
Dominant' traits will actually disappear faster if they are disadvantageous.
Think about it: if everyone who has even a single copy of a particular allele is at a disadvantage (manifests the phenotype, in this case six fingers), then even single copies are selected against.
In the case of recessive traits, selection occurs only against homozygous carriers, who may be very rare if the allele itself is rare.
A concrete example would be something like Tay-Sachs disease. If the allele that causes this were dominant, every carrier would die before adulthood, and it would occur only as a very rare de novo mutation. But because it is recessive, it persists for now; heterozygous carriers have no disadvantage.
The right lung<span> has </span>both<span> more </span>lobes<span> and segments than the left. It is </span>divided into <span>three </span>lobes<span>, an upper, middle, and a lower, by </span>two<span> fissures, one oblique and one horizontal. The upper, horizontal fissure, separates the upper from the middle </span>lobe<span>.</span>
Answer:
<em>This question includes the following options:</em>
<em>A.</em><em>1 - </em><em>B.</em><em>3 - </em><em>C.</em><em>6 - </em><em>D</em><em>.8 -</em><em> E.</em><em> 12</em>
PCR which stands for <em>"Polymerase Chain Reaction"</em> is a molecular biology procedure to quickly multiply a small sample of DNA into millions or billions of DNA copies for studying purposes.
<em>"Unlinked"</em> signifies that the markers are present in 6 various chromosomes, but to amplify those markers we would need <em>(</em><em>12</em><em>)</em> unique primer sequences, due to it is required to have the reverse and forward primers for every marker; thereby the answer is <em>(</em><em>E.</em><em>)</em>
