Translation requires some specialized equipment. Just as you wouldn't go to play tennis without your racket and ball, so a cell couldn't translate an mRNA into a protein without two pieces of molecular gear: ribosomes and tRNAs.<span>Ribosomes provide a structure in which translation can take place. They also catalyze the reaction that links amino acids to make a new protein.</span><span>tRNAs (transfer RNAs) carry amino acids to the ribosome. They act as "bridges," matching a codon in an mRNA with the amino acid it codes for.</span>Here, we’ll take a closer look at ribosomes and tRNAs. If you're not yet familiar with RNA (which stands for ribonucleic acid), I highly recommend checking out the nucleic acids section first so you can get the most out of this article!Ribosomes: Where the translation happensTranslation takes place inside structures called ribosomes, which are made of RNA and protein. Ribosomes organize translation and catalyze the reaction that joins amino acids to make a protein chain.
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In addition to the local control of blood flow, global control of blood flow including changes in cardiac output and control of arterial BP is mediated by the autonomic nervous system. Global neural control of arterial hypertension is essentially through the sympathetic nervous system (SNS).
Explanation:
From Google
Answer:
A series if reaction break and rrarrange csrbon bonds to release energy ang carbon dioxide.
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A Ligase
B False
C To separate the double‑stranded DNA
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The Polymerase Chain Reaction (PCR) is a technique widely used in molecular biology laboratories in order to make millions of copies of a specific sequence of DNA. PCR requires deoxynucleotide triphosphates (dNTPs) to synthesize new copies of the target DNA fragment, a thermostable DNA polymerase that adds nucleotides to new DNA strands, and primers that attach to complementary ends at each DNA strand. PCR has three phases: 1-Denaturation, where the double-stranded DNA molecule is heated to separate it into two single (separated) strands; 2-annealing, where the temperature is lowered in order to allow the primers to attach each DNA strand, and 3- extension, where the temperature is increased (again), and the thermostable DNA polymerase adds the appropriate dNTPs to new DNA strands. In consequence, annealing occurs at the lowest temperature. Moreover, during the denaturation stage, the temperature is increased at 90–95°C in order to denature the DNA strands into single strands.
