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creativ13 [48]
4 years ago
5

Ugg sorry posting so much but now I cant edit! Yes this is what the other 2 are

Biology
1 answer:
RideAnS [48]4 years ago
8 0

Enzyme notes :

- Many chemical reactions can be speed up by substances called catalyst.

- Metabolic reaction (chemical reaction) is controlled by enzyme.

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Pedigrees are used to help geneticists understand how traits are inherited between generations. The Romanovs, a Russian royal fa
inysia [295]

Answer:

Waldemar carried the recessive allele.

Explanation:

The carrier is the individual that has the affected allele or mutation but does not express the trait, or might express it in different levels. Although, as the person carries the mutation, she or he might transmit the genetic mutation associated with a disease to the progeny.  In general, these diseases are inherited as recessive traits.

So, in the exposed example we know that:

  • hemophilia is a sex-linked disorder
  • hemophilia is determined by a recessive allele on the X chromosome.
  • Irene is a carrier.
  • Her husband is not a carrier.
  • Her children Waldemar and Henry have hemophilia.

If Irene is a carrier, this means that she is heterozygous and that her genotype is X⁺X⁻ (Being the symbol + the dominant allele, and - the recessive one for that expresses the trait)

The fact that Irene´s husband is not a carrier means that his genotype is X⁺Y

Their boys Waldemar and Henry have hemophilia, so both their genotypes are X⁻Y

The best evidence to prove that Irene was heterozygous for hemophilia is that Alice carried the recessive allele.

  • Alice is Irene´s Mother, and she is a carrier as well. Irene´s father, Louis, is not a carrier, so she could have inherited a dominant allele from her father and a recessive allele from her mother, X⁺X⁻, or she could have inherited two dominant alleles from both her parents X⁺X⁺. This is not proof enough of Irene being heterozygous.
  • The fact that Alexandra, Irene´s sister, was also a carrier does not say anything about Irene´s genotype, because they could both share the same genotype or not. This is not proof of Irene being heterozygous.
  • Frederick (her brother) was hemophilic.  He received a recessive allele from Alice, but this does not say anything about Irene´s genotype.  
  • The fact that Waldemar (her son) was hemophilic, is the best evidence to prove that Irene was heterozygous for hemophilia. Walderman received the Y chromosome from his father and an X chromosome from his mother. The X chromosome that he received from his mother carried the recessive allele for the trait, and this is why he had hemophilia. This means that there is no best evidence for Irene´s genotype than her son´s genotype.

 

6 0
4 years ago
Which type of bond is formed in nitrogen gas?
Nesterboy [21]

Answer:

Covalent bonds are formed in the nitrogen gas.

Explanation:

"<em>Nitrogen atoms will </em><em>form three covalent bonds</em><em> (also called triple covalent) between two atoms of nitrogen because each nitrogen atom needs three electrons to fill its outermost shell</em> (Lumen Learning)."

I hope this helps! Have a great day!

7 0
3 years ago
Read 2 more answers
Hello good afternoon what is mitochondria​
Slav-nsk [51]

Answer:

A mitochondrion is a double-membrane-bound organelle found in most eukaryotic organisms. Mitochondria generate most of the cell's supply of adenosine triphosphate, used as a source of chemical energy. They were first discovered by Albert von Kölliker in 1880 in the voluntary muscles of insects.

6 0
3 years ago
Read 2 more answers
NECESITO AYUDA SINCERA
Leona [35]
Creo que es D (el coleccionismo) porque eso no tiene sentido
3 0
4 years ago
nucleotide substitutions occur by mistake in a segment of ribosomal rna at a constant rate of one substitution every 100,000 yea
harkovskaia [24]

The number of years of divergence from a common ancestor =300,000 years.

<h3>What are mutations?</h3>

Mutations are changes that occur in the DNA of living organisms.

Mutations can be used as molecular clocks if they occur at a constant rate.

Considering the nucleotide substitutions occur by mistake in a segment of ribosomal RNA at a constant rate of one substitution every 100,000 years.

The ribosomal RNA of the two modern-day species have six differences in their sequences.

Number of years of divergence = 6/2 * 100000 = 300,000 years.

In conclusion, changes that occur in nucleotide sequences are known as mutations.

Learn more about mutations at: brainly.com/question/12572634

#SPJ1

4 0
1 year ago
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