Answer:
A) AUG GAG GGU
B) N-MET-GLU-GLY-HIS
C) 10 amino acids
D) The stop codon here is UAA, instead of UAG. If a tryptophane residue is added where the stop codon is, the GEN polypeptide would be longer
Explanation:
First we must obtain the the complementary chain or mRNA
A) AUG start codon is complementary to DNA TAC triplet, and GAG is complementary to CTC, and GGU to CCA (running from left to right towards 5'DNA direction (AAGCGGATACCTCCCAGTAGATGCTCCGGGGCTAGTGATTTCGAAC-5)
B) TAC corresponds to Methionine, GAG to Glutamate, GGU to Glycine, and CAU to Histidine
C) UAA is the stop codon, that is complementary where the DNA triplet is ATT. From AUG to UAA, we can have 10 amino acids transcribed
D) If a trp is included where the stop codon is UAA, then the mRNA would be longer with a consequent traduction of a longer GEN polypeptide
Answer:
your answer is c
Explanation:
telophase
Mitosis ends with telophase, or the stage at which the chromosomes reach the poles. The nuclear membrane then reforms, and the chromosomes begin to decondense into their interphase conformations. Telophase is followed by cytokinesis, or the division of the cytoplasm into two daughter cells.
hope this help
The distance between peaks of a wave
Answer:
The correct answers are
Question a) "50%".
Question b) "66%".
Explanation:
Achondroplasia is caused by a dominant allele, which means that a person with a "A" allele will develop this condition. In this case, all the people with Achondroplasia are heterozygotes "Aa" because the dominant genotype "AA" causes prenatal death. If a person with achondroplasia "Aa" mates with a person of average height "aa", the expected percentage of children with average height will be 50%, since there are 50% of chances of having "aa" children and 50% chances of having "Aa" children. Also, If two persons with achondroplasia have children ("Aa" x "Aa") , the expected percentage of children with achondroplasia will be 66%. The probability of having children with the "Aa" genotype is 50%, however since the "AA" genotype causes prenatal death, this genotype is not considered in the percentage.