Answer:
mitochondria
Explanation:
Both bacteria and mitochondria have their own cell
Answer:
Explanation:
The Genotype of the woman is XCbXN
The man XNY
Since the allele for the color blindness is carried on one of the X -chromosomes of the carrier mother, then the male children will be color blind or carrier deopending on the defective gene they inherited. Since they will receive the defective or normal allele from the mothers,but the female will carriers or normal because they will inherit either defective allele or normal allele from the mother,but normal X allele from the father.
Assuming the colorbind gene was inherited by One of the boys, and the girls take the defective genes
1. XNY vs XCbXN.Then the one of the boys will be colorblind and the one of girls will be carriers. XNXCb, XNXN, XCbY,XNY 50 %
2.If the two boys take the effective genes from the mothers. and none of the girls take the defective alelle
Then the two boys will be colorblind and the girls will be carrries XcbY,XcbY and XNXN XNXN.(normal girls).
The proportions that will be the females since the girls can only take the defective allele from one of the normal and defective allele from the mother. Assuming the girls take the defective allele from the mothers and take normal from the father,they will all be carriers,since the X of the father is normal.
They can not have a color blind girl.Since the father is normal It takes two colorblind X-chromosome to give a girl.
Answer:
When a nerve impulse reaches the end of an axon, the axon releases chemicals called neurotransmitters. Neurotransmitters travel across the synapse between the axon and the dendrite of the next neuron.
Explanation:
The binding allows the nerve impulse to travel through the receiving neuron.
Ans.
The codons show genetic codes, made up of triplet of nucleotides in DNA or RNA that code for specific amino acids. The different codes can code for a same a amino acid. When a substitutional mutation occurs in genetic material, it shows substitution of one nucleotide pair for another and leads to formation of a different codon.
The first mutation that leads to CAU to CAC, it will not show any potential damage as both CAU and CAC codons code for histidine amino acid.
The second mutation that leads to UGU to UGC will also not show any damage to protein as both of these codons code for cysteine amino acid.
The third codon, that results UCU to UUU will cause a potential damage to protein as UUU codes for phenyl alanine (an aromatic, non-polar amino acid) and UCU codes for serine (a polar amino acid).
Thus, the correct answer is 'option C).' as in a protein, substitution of serine with phenylalanine will lead to change in structure and function of that protein.
Maybe it’s not a mineral because it’s just hardened tree resin whereas minerals can be mined and found deep in the earth…?
