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Nucleic acid extraction consists of three major processes: isolation, purification, and concentration. Commercial extraction kits are commonly used in the clinical microbiology laboratory [2]. These kits provide the essential requirements for nucleic acid extraction.
Nucleic acids are polynucleotidesthat is, long chainlike molecules composed of a series of nearly identical building blocks called nucleotides. Each nucleotide consists of a nitrogen-containing aromatic base attached to a pentose (five-carbon) sugar, which is in turn attached to a phosphate group.
The two main classes of nucleic acids are deoxyribonucleic acid (DNA) and ribonucleic acid (RNA).
Solution-based methods Cesium Chloride Gradient Centrifugation (with Ethidium Bromide) This method is based on the phenomena of buoyant and specific density. Guanidinium Thiocyanate-Phenol-Chloroform nucleic acid extraction. Cetyltrimethylammonium Bromide nucleic acid extraction. Chelex Extraction. Alkaline Extraction.
Types of nucleic acid extraction Guanidinium Thiocyanate-Phenol-Chloroform Extraction. Cesium Chloride / Ethidium Bromide Gradient Centrifugation. Solid-Phase Extraction. Magnetic bead-based purification.

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The rules of base pairing (or nucleotide pairing) are: A with T: the purine adenine (A) always pairs with the pyrimidine thymine (T) C with G: the pyrimidine cytosine (C) always pairs with the purine guanine (G)
Basic Isolation Procedure Creation of Lysate. The first step in any nucleic acid purification reaction is releasing the DNA/RNA into solution. Clearing of Lysate. Binding to the Purification Matrix. Washing. Elution.
These include PCR, RT PCR, sequencing and blotting. There are also techniques such as EMSA, footprinting, ChIP and probing that detect inter-molecular interactions of nucleic acids. Research in nucleic acids involves the isolation and characterization of DNA and RNA molecules from various cells, tissues, and organisms.

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