Answer: The options are not included.
But the sites are;
Interaction with ribosomes.
Interaction with aminoacyl tRNA
synthase.
Attachment of the specific Amino acid.
Interaction with codon.
Explanation:
Transfer RNA is a type of RNA that help to translate messenger RNA sequence into protein. Each tRNA have two major areas; the anticodon and region for attaching specific Amino acids.
tRNAs function at specific sites in the ribosomes during mRNA deciding.
The four specific recognition sites of trna that must be inherent in it's tertiary structures in order for it to carry out it's role are;.
Interaction with ribosomes.
Interaction with aminoacyl tRNA synthase.
Attachment of specific Amino acid.
Interaction with codon.
Flower bearing that is simple my step mom drinks it!
Part 1.
The correct answer is option 2.There are two alleles for freckles.
According to the condition of the occurrence of the freckles, it can be concluded that the freckle is an autosomal dominant condition. The freckle can only be inherited, if there is at least one dominant allele in any of the parent. If both the individuals are heterozygous for the trait, they can produce an offspring without freckle by passing down the recessive alleles to the progeny. So, the freckles are controlled by two alleles, which can be either dominant or recessive.
Part 2.
The correct answer is option 4. P generation and F2 generation.
In this case, it is given that true bred homozygous recessive plant is crossed with true bred homozygous dominant plant. The true bred recessive plant always shows the recessive phenotype. When true bred homozygous recessive plant is crossed with true bred homozygous dominant plant, the F1 generation would produce all the heterozygous individual and exhibit dominant phenotype. When the F1 generation is self crossed, it result in 75% dominant phenotype and 25% recessive phenotype.
A possible cross for this case is given in the picture.
The answer is Glomerulonephritis, the patient would show data that suggest they have the presence of that disorder.
Answer:
e is correct
Explanation
:
Phosphorus is critical because this element is required for enzymatic activities that take place during glycolysis, in the metabolism of glutamine to form ammonia (ammoniagenesis) and also in oxidative phosphorylation, where the cells produce energy from the generation of ATP from ADP.
In serum (blood plasma), the inorganic phosphate is combined with oxygen (O2) to form diverse types of phosphates (PO4) molecules that play key functions in muscle activity, nervous system development, and bone growth.
Serum phosphate is a critical buffer that maintains the acid‐base balance in the urine. The serum phosphate level in an adult must be in the range of 2.5 to 4.5 mg/dl, being higher levels indicative of hyperphosphatemia. This inorganic phosphate has important functions during the ATP synthesis, cyclic AMP, post-translational modification (i.e., protein phosphorylation), and also as an intracellular buffer.
