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xxTIMURxx [149]
3 years ago
11

One spot on the microarray contains sequences unique to a gene for an RNA polymerase subunit. One spot contains sequences unique

to the skeletal muscle myosin gene. Which spot would be expected to contain the myosin gene sequences
Biology
1 answer:
AVprozaik [17]3 years ago
6 0

Answer:

Skeletal muscle myosin gene

Explanation:

A microarray assay (also named DNA chip or biochip) is an approach used in molecular biology to detect simultaneously the expression level of hundreds of genes at the single-cell level. First, the complementary DNA (cDNA) sample is obtained from the total RNA sample. Subsequently, the cDNA is cut with restriction endonucleases and fluorophores are attached to them. Finally. the DNA fragments react with complementary known sequences (also known as probes) in order to identify by fluorescence the genes that are expressed in the sample.

Myosin is a superfamily of proteins responsible for generating the muscle contraction force both in animal and human muscle cells. In this case, the probe corresponds to the complementary sequence of the myosin gene, thereby the binding evidenced the expression of the myosin gene in the cDNA sample.

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How are solar cells used today?
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Thinking creatively about evolutionary mechanisms, identify at least two schemes that could generate allelic polymorphism in a p
Ede4ka [16]

Complete question:

Thinking creatively about evolutionary mechanisms, identify at least

two schemes that could generate allelic polymorphism in a population except natural selection that favors heterozygotes.

<u>Select the two correct answers.</u>

-inbreeding among individuals in the population

-purifying selection against mutational variants of alleles in the population

-continuous migration of individuals with new alleles into the population

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-genetic drift of alleles common in the population

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Answer:

The two events that might favor heterozygotes among the options are  

  • The Continuous migration of individuals with new alleles into the population
  • Mutations that do not severely affect viability and reproductivity.  These might favor heterozygous frequencies.

Explanation:

Due to technical problems, you will find the complete explanation in the attached files.

Download pdf
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2 years ago
What statement best describes what happens to a substrate after it bonds to an enzyme?
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8 0
3 years ago
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I WILL GIVE BRAINLIEST!!!
Nesterboy [21]

Answer:

25%

Explanation:

When looking at a pedigree remember that:

  • squares are males
  • circles are females
  • the solid colored figure represents an individual affected by a disease
  • the empty figure represents a healthy individual

Let us assign the symbol X⁺ to represent the dominant allele linked to the X-chromosome and expressing healthiness, and X⁻ to represent the recessive allele expressing the dissease.

According to this pedigree

  • I1 is a man affected by the disease, YX⁻
  • I2 is a healthy woman X⁺X⁻
  • we can see that among the progeny (generation II) there are two individuals affected (a boy and a girl) and one healthy girl. This means that the mother I2 is heterozygous for the trait.

So, having their genotypes we can know what are the probabilities of getting a son with DMD

Parentals)    YX⁻     x     X⁺X⁻  

Gametes)   Y     X⁻      X⁺     X⁻

Punnett square)

                        X⁺             X⁻

            X⁻      X⁺X⁻         X⁻X⁻    

            Y        X⁺Y           X⁻Y

F1)

  • The probabilities of getting a healthy daughter X⁺X⁻ are 25%
  • The probabilities of getting a healthy son X⁺Y are 25%
  • The probabilities of getting a daughter with DMD X⁻X⁻ are 25%
  • The probabilities of getting a son with DMD X⁻Y are 25%
7 0
2 years ago
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