Answer:
DNA molecular weight standard controls, also known as DNA ladders
Explanation:
A DNA ladder is a molecular-weight size marker used to identify the size of the PCR products in a gel electrophoresis. The DNA ladder consists of a solution containing double-stranded DNA fragments with different molecular weights including, among others, 50 base pairs (bp), 100 bp, 1000 bp and 3000 bp DNA fragments. The concentration of each DNA fragment in the DNA ladder must be sufficiently high to be visualized on the electrophoresis gel.
Create the inverse DNA<span> or </span>RNA<span> strand. For example, the sequence "ATGC" is converted to "CGTA". Replace thymidine (T) by uracil (U). For example, the sequence "ATUGC" is converted to "AUUGC".</span>
MRNA, is used to transcript DNA codes from DNA molecules and then later exits the nucleus via nuclear pore, then moves to the ribosome. Then, tRNA is activated to bring specific amino acid to the ribosome for translation. Ribosome, which is the site of synthesis of proteins, is composed of rRNA and ribosomal proteins.
A codon is a three-base sequence (three nitrogen bases in a row) on mRNA. An anticodon is a three-base sequence on tRNA. It matches the codon.
Answer:
By 1900, Fingerprint was the evidence which was collected at crime scenes to help positively identify suspects by one particularly unique trait. No two people can have the same type of fingerprints. It is a unique characteristic which is even not common among identical twins. Therefore, was considered as an important evidence for identification of suspects and linking them with the scene of offence. In 1904, the city of St.Louis, Missouri used fingerprint evidence for the first time for criminal identification.