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Summary Separation and Visualisation of Nucleic Acids

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A brief detailed summary of the essentials of nucleic acid quantification. Dive into key techniques like spectrophotometry and fluorometry, and discover how gel electrophoresis plays a vital role in assessing sample integrity. Perfect for students in all years of university. Whether you're preparin...

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  • January 13, 2025
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  • 2024/2025
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Summary Notes

Separation and Visualization of Nucleic
Acids

1. Quantification of Nucleic Acids
 Quantification of nucleic acids, such as DNA and
RNA, determines their concentration and purity in
a sample. This process is crucial for downstream
applications like PCR, sequencing, and cloning.
Common techniques include spectrophotometry
using a NanoDrop (measuring absorbance at 260
nm for nucleic acids and 280 nm for proteins) and
fluorometry, which uses fluorescent dyes specific
to nucleic acids for more sensitive detection.
Example:
Using a NanoDrop, a researcher measures the
absorbance of an RNA sample. The absorbance ratio at
260/280 nm is 1.8, indicating good purity, and the RNA
concentration is 50 ng/μL. This RNA can now be used
for cDNA synthesis in a reverse transcription PCR
experiment.




NanoDrop Device

, 1.1 Gel Electrophoresis
 Separation of molecules based on relative
migration through a gel across an electric field.



Two main types:
1. Agarose gel electrophoresis
- Typically used for separation nucleic acid molecules
ranging from 100 bp to 100 kbp) – static electric field
- Two variants:
~ Pulse field gel electrophoresis (PFGE) & Field inversion
gel electrophoresis (FIGE): used for separating larger
molecules
e.g. from 50 to 1000 kb
2. Polyacrylamide gel electrophoresis
(PAGE) < 100bp
- resolution to the base pair.


~ While spectrophotometry (e.g., NanoDrop) and
fluorometry measure concentration and purity, gel
electrophoresis complements these methods by
assessing the integrity and size of nucleic acids.


How They Are Linked:
~ Integrity Assessment: Gel electrophoresis helps verify if
the DNA or RNA is intact or degraded, which is crucial for
accurate quantification. For example, smeared RNA on a
gel indicates degradation, even if spectrophotometric
measurements suggest high concentration.
~ Verification of Results: After quantifying nucleic acids,
running a gel ensures the sample is free of contaminants

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