Answer:
The correct answer would be "Myosin heads attach to sites on actin filaments".
The muscle cell or myofibril consists of two types of protein filaments namely; actin (thin filament) and myosin (thick filament).
The myosin heads attach to the binding sites on the actin filaments and pull it towards the M-line in order to produce contraction.
The hydrolysis of ATP provides energy for this contraction cycle.
Answer:
His body would most likely not become entirely immune to the same pathogen, but there are at least two outcomes that could occur, he can become more susceptible to getting the pathogen again, now that it has already affected his body once, or his body would be more equipped to protect itself against the pathogen.
Answer:
D. A, B, AB, or O
Explanation:
We can start by visualizing all the possible genotypes of the offspring by drawing a Punnett square, which is a visual representation of the different possible combinations of alleles:
Individual 1 = AO, Individual 2 = BO
A O
B AB BO
O AO OO
Here we can see that there are 4 possible genotypes: AB, BO, AO and OO based on the alleles of the parents. Now we can match the genotypes to phenotypes to answer the question:
A and B are codominant, meaning that both will be expressed equally if both are present. Therefore the genotype AB will result in an AB phenotype.
Next, since A and B are both dominant over O, they are the alleles that will be expressed in the phenotype if paired with an O. This means that the genotype AO will result in an A phenotype, and likewise, genotype BO will result in phenotype B.
Finally in the genotype OO, although O is a recessive allele, there are no dominant alleles here to mask them, therefore O is expressed in the phenotype.
Hence, from the genotypes AO and BO, the possible offspring genotypes are AB, BO, AO and OO, translating to the possible phenotypes: A, B, AB or O.
Hope this helped!
<span>The correct answer is letter A, disorders in individual genes are responsible for Down's syndrome.
This is a human genetic disorder that is associated with physical growth delays, characteristic facial features, and a mild to moderate intellectual disability. This is a condition in which the genes make a copy of the chromosome 21. </span>
