Gel electrophoresis - eco r1 digest with lambda

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In summary, an Eco R1 digest of lambda produces six fragments, two of which are almost the same length. Since these two fragments produce the same band on a .8% agarose gel, the 21.2 kb fragment is not visible.
  • #1
kazz143
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just want to know why if there are six fragments present in an Eco R1 digest of lambda then why are there only five bands visible on a .8% agarose gel? so where have the 21.2 kbp gone? is it to big to migrate therefore has not show up on the gel? can someone explain to me please? thankyou
 
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  • #2
A few possibilities come immediately to mind, but no way for me to know if any of them are what happened in your case. You may have gotten an incomplete digestion, you might have run the gel too long or too short of a time so either ran a band off the end or didn't get full resolution of all the bands, you might have had insufficient ethidium bromide, or it wasn't uniformly mixed through your gel, so couldn't detect a band, or your band might have been too faint to see.
 
  • #3
Larger fragments are usually easier to see (more EtBr incorporation). However, 21.2 kb is pushing a 0.8% agarose gel. As a rule of thumb, the maximum resolution to be expected for a 0.8% gel is around 0.5-5 kb. Did you run a marker with a relevant size?Also consider that the overall gel size is also an issue. In mini-gels it is kinda tricky to resolve that size.
If the agarose is of good quality you can try to go down to 0.6%.
 
  • #4
hey thanks for ur posts. i understand now the 21.2 kbp is not the missing one. its becasue in an ecor1 digest of lambda it produce 6 fragments two of which are alomost the same length i.e the 5.6 and 5.8 kbp therefore we can only see 5 bands not 6 becasue the have migrated at the same pace to almost the same place donw the gel resulting in oine large band hard to tell that dere is actually two bands. thanks heaps newase
 

1. What is gel electrophoresis?

Gel electrophoresis is a laboratory technique used to separate and analyze DNA, RNA, or protein molecules based on their size and charge. This is achieved by applying an electrical current to a gel matrix, causing the molecules to migrate through the gel at different rates.

2. How does eco r1 digest work in gel electrophoresis?

Eco r1 digest is a restriction enzyme that recognizes and cuts specific DNA sequences. In gel electrophoresis, eco r1 digest is used to digest the DNA sample, creating fragments of varying sizes. These fragments are then separated and visualized on a gel to analyze the DNA sequence.

3. What is lambda in gel electrophoresis?

Lambda (λ) is a commonly used DNA marker in gel electrophoresis. It is a standard reference DNA fragment of known size that is used to compare and determine the sizes of other DNA fragments in the sample.

4. What is the purpose of using eco r1 digest with lambda in gel electrophoresis?

The combination of eco r1 digest and lambda in gel electrophoresis allows for accurate sizing and comparison of DNA fragments in the sample. The restriction enzyme creates fragments of different sizes, and the lambda marker provides a reference for determining the sizes of these fragments.

5. What are the applications of gel electrophoresis - eco r1 digest with lambda?

Gel electrophoresis - eco r1 digest with lambda is commonly used in molecular biology and genetics research for DNA analysis, such as identifying genetic mutations, studying gene expression, and analyzing DNA sequences. It is also used in medical diagnostics, forensic science, and biotechnology industries.

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