please answer them as much as possible thanks so much!!
1. What is the basis for separation of DNA fragments using gel
electrophoresis?
2. What is the purpose of a “running buffer”?
3. How many microlitres (µL) are in one millilitre (mL)?
4. If the DNA solutions provided were 10µg/mL and you loaded 5µL on the gel,
how many µg of DNA were loaded in each well?