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You could use other enzymes or use a higher percetage of agarosa to make your gel (so they will have a better chance of separating). Or try polyacrilamide. It should solve those bands even better.

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Q: What could be done to resolve the fragments?
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Two small restriction fragments of nearly the same base pair size appear as a single band even when the sample is run to the very end of the gel What could be done to resolve the fragments?

Increase the density of the gel. This will slow down the denser fragment while speeding up the less dense fragment. The down side is that the denser fragments near the beginning of the gel near the DNA well will be seen as a single band.


Are moon fragments part of a moon?

Moon fragments could be part of the moon as well as external bodies that have hit the lunar surface such as asteroids and meteorites.


Why would a scientist use a higher versus a lower percent agarose solution when preparing a gel to separate DNA?

Different percentages have different resolving powers. There is no one agarose percentage that is suitable for all sizes of DNA - you must chose the percentage best for resolving the sizes of DNA you are examining. If your agarose concentration is too dense for the size of your DNA fragments, the DNA will barely migrate through the gel. If the agarose concentration is too dilute for the size of your DNA, it will run straight through the gel without resolving into sharp bands. Generally speaking you use higher percentages if you want to resolve smaller DNA fragments and lower percentages if you want to resolve larger DNA fragments. Small DNA fragments need high percentages or else they'd run straight through the gel without being resolved into bands. Large DNA fragments need low percentages to permit them to migrate into the gel.


Can mudstone fragments be easily seen?

No. The fragments in mudtsone are microscopic if not submicroscopic.


What are two examples of sediment?

1. mineral fragments 2. rock fragments

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What could be done to resolve two fragments that are nearly the same base-pair length and did not appear on the electrophoresis gel?

You could use other enzymes or use a higher percetage of agarosa to make your gel (so they will have a better chance of separating).


Two small restriction fragments of nearly the same base pair size appear as a single band even when the sample is run to the very end of the gel What could be done to resolve the fragments?

Increase the density of the gel. This will slow down the denser fragment while speeding up the less dense fragment. The down side is that the denser fragments near the beginning of the gel near the DNA well will be seen as a single band.


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What could be a sentence with the word resolve?

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Configure the users with a higher security macro setting.


Are moon fragments part of a moon?

Moon fragments could be part of the moon as well as external bodies that have hit the lunar surface such as asteroids and meteorites.


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What can be done to help resolve the gender issue in the computing field?

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