Answer: c) amino acid
Explanation: A codon is an mRNA sequence which contains three nucleotides that codes for a particular amino acid. The codons on the mRNA are read by the ribosome during translation and the amino acid coded for by each codon is used to make a protein. There are 64 different codons in existence, each amino acid is coded for by at least one codon. Some amino acids have more than one codon. For example, the amino acid Leucine is coded for by six codons: UUA, UUG, CUU, CUC, CUA and CUG while the amino acid phenylalanine is coded for by two codons: UUU and UUC.
OK so I'll give you two examples you can catch it if someone who is infected coughs or sneezes so basically it can be spread via airborne or you can even get it from sharing food or drinks also the best way to get rid of strep will be antibiotics/over the counter medicines or gargling warm salt water
Answer:
RNA polymerase binds to the promoter
Polymerase initiates RNA synthesis at the start point on the template strand
RNA polymerase moves downstream unwinding the DNA
RNA transcript is released and polymerase detaches from the DNA
The pre-RNA undergoes processing
Explanation:
The promoter is the specific DNA sequence that serves as a binding site for RNA polymerase. The enzyme RNA polymerase recognizes the promoter sequence and binds to it to begin the process of RNA synthesis. The process of RNA synthesis begins at the start site where the process of the unwinding of DNA duplex is initiated.
The unwinding separates the two DNA strands at the start site where RNA polymerase begins the process of synthesis of the new RNA strand. The newly formed RNA strand and RNA polymerase are released from the template strand after the termination of the process.
In eukaryotes, the primary RNA transcript undergoes the process of splicing of introns, the addition of poly-A tails and 5' cap which in turn transform it into the mature mRNA.
Answer:
These bands represent different confirmation of DNA
Explanation:
pGLO DNA is a plasmid DNA that is used as a vector for genetic engineering. Plasmid DNA is found in supercoiled confirmation in vivo. The double helix forms extra twists to easily fit inside the cells. During isolation of plasmid from the cell, nicks can be introduced in the DNA due to harsh isolating methods or contamination by nuclease. As a result the supercoiled confirmation is changed into circular confirmation. It is bulkier than the supercoiled form and travels more slowly. When both DNA stands get cut at the same place, the DNA gets liner confirmation. In the end, supercoiled DNA runs the fastest on gel followed by linear DNA and then the circular DNA.
