The answer is 25%
When you make a punnet square 1/4 boxes has rr which is the only one that is a wrinkled seed
Answer:
TEs are repetitive and mobile elements, thereby it is hard to trace their origins
Explanation:
Repetitive elements are patterns of nucleotide sequences in the DNA characterized to have multiple copies throughout the genome. DNA mini-satellite and Transposable Elements (TEs) are some examples of highly repetitive DNA. TEs are repetitive mobile elements that have the ability to jump within the genome and occupy a major part of eukaryotic genomes. For instance, there is a type of TEs called retrotransposons which mobilize through a copy-and-paste mechanism, thus increasing their number in a genome. In consequence, TEs represent highly repetitive and dynamic genomic sequences, and thereby it is hard to trace their evolutionary histories.
B.False
Because starch is the storage form of glucose in plants, and glycogen as the storage carbohydrate in animals
Answer:
Gamete of organism has a haploid number of chromosomes.
2n = 30
n = 15
A diploid cell containing 30 chromosomes will result in 15 chromosomes in each of the 4 daughter cells after meiosis occurs.
After first nuclear and cellular division (Meiosis I), each daughter cell will only have 15 chromosomes as homologous chromosomes are broken apart at Anaphase I of meiosis I. Chromosomal number is halved. After the second nuclear and cellular division (Meiosis II), each daughter cell will also have 15 chromosomes. This time, instead of the chromosomal number being halved, their chromosomal contents are halved. Sister chromatids are separated at Anaphase II of Meiosis II, resulting in daughter chromosomes each.
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Explanation:
Answer:
A single nucleotide changes in CCG which will result in missense mutation can be many possibilities.
Explanation:
Missense mutations
CCG codes for Proline amino acid
• Mutation in first nucleotide codes for
UCG specifically encodes Serine
ACG specifically encodes Threonine
GCG specifically encodes Alanine
Missense mutation
• Mutation in second nucleotide specify for coding
CUG specifically encodes Leucine
CAG specifically encodes Glutamine
CGG specifically encodes Arginine
• Mutation in Third Nucleotide will not result in missense mutation because any point mutation in third nucleotide of codon will encode same amino acid i.e Proline.
