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In molecular biology, a hybridization probe is a fragment of DNA or RNA of variable length which can be radioactively or fluorescently labeled. It can then be used in DNA or RNA samples to detect the presence of nucleotide substances that are complementary to the sequence in the probe.DNA probes are stretches of single-stranded DNA used to detect the presence of complementary nucleic acid sequences (target sequences) by hybridization. DNA probes are usually labelled, for example with radioisotopes, epitopes, biotin or fluorophores to enable their detection.
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En biología molecular, una sonda de hibridación es un fragmento de ADN o ARN de longitud variable que puede marcarse de forma radiactiva o fluorescente. Luego puede usarse en muestras de ADN o ARN para detectar la presencia de sustancias nucleotídicas que son complementarias a la secuencia en la sonda. Las sondas de ADN son tramos de ADN monocatenario utilizados para detectar la presencia de secuencias complementarias de ácido nucleico (secuencias diana) por hibridación Las sondas de ADN generalmente están marcadas, por ejemplo, con radioisótopos, epítopos, biotina o fluoróforos para permitir su detección.
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Sadly the peafowl are unable to swim, they have four toes on their feet. Three toes face forward and one toe faces backwards. This unique combination of toes enables the peacock to perch easily on branches of trees. They do not have webbed feet which are necessary for birds to actively swim.
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Here is ur answer.
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The answer is pp
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Steve and Sonya's son genotype is pp. Because an inheritance of autosomal recessive disorder is with recessive allele responsible for the exceptional phenotype. In this case, Steve and Sonya are both heterozygotes, Pp, which means they both have a p allele because each one gave the boy a p, contributing to affect his son. And since we are talking about inheritance of an autosomal disorder, we know that the parents phenotypic proportions are the same.
The answer is a pedigree chart.
<span>Pedigree charts are used to explain the occurrence of particular genes from one generation to the next. It gives enough information about family disease history. They are used in families to find out the probability of inheriting some disease. So, if Maria and Juanita are cousins and the genotypes of other members of their family are known, the pedigree chart could predict their genotypes. Still, it is not as precisely as DNA test.</span>
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A) Resources become scarce.