DNA Extraction and Analysis Quiz

Commonly employed method involving phenol and chloroform to isolate DNA from cells.

The main purpose is to separate DNA from other cellular components for further analysis.

DNA amplification is not a step in the DNA extraction process; it is a separate process.

Ethanol or isopropanol is added to precipitate DNA, separating it from the solution.

Mitochondria are a common source of DNA for extraction due to their distinct DNA.

Buffer solution helps maintain pH and prevents denaturation of DNA during extraction.

Protease is employed to degrade proteins and facilitate DNA extraction.

Polymerase Chain Reaction is a technique to amplify DNA for analysis.

Sanger sequencing is a common method for determining the sequence of DNA bases.

DNA ladder helps estimate the size of DNA fragments in gel electrophoresis.

Bisulfite sequencing is a method used to study DNA methylation patterns.

DNA polymerase in PCR synthesizes new DNA strands during the amplification process.

Southern Blotting is employed to visualize DNA fragments separated by gel electrophoresis.

Northern Blotting is employed to analyze gene expression at the RNA level.

Multiplex PCR enables the simultaneous detection of multiple DNA sequences in a single reaction.

ChIP-seq analyzes DNA-protein interactions based on their affinity and physical association.

Southern Blotting studies DNA-protein interactions based on their affinity and physical association.