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Q: Is loading dye same with binding dye in electrophoresis?
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Definition of DNA loading dye?

Loading dye is a substance commonly used in labs and the study of genetics. It causes DNA to become clearer under a microscope by tinting it purple.


What is a sentence using the word dye?

As a verb: I will dye the drapes to match the new furniture. As a noun: I spilled some dye on my best shirt. As an adjective: Be sure all of the skeins of yarn have the same dye lot number.


What is the function of the blue dye added to the sample before the electrophoreses is performed?

The blue dye is usually a combination of glycerol and something else. But I believe the most important part is the glycerol. Glycerol is heavier than the buffer that you actually perform the electrophoresis in.By adding the glycerol to your sample, you give it weight so that it doesn't float around when you're trying to pipette it into your well and so that it will just fall.


Why does dye spread through all the clothes in washing machine?

Dye spreads through the clothes in a washing machine when it starts rinsing. Whilst it is rinsing, the water will pick up the dye and then start it's usual spin, this will cause the dye to go all about the washing machine and the clothes pick it up ( The same principals of getting a stain on your t-shirt ), only when a dye is used the chances are it won't come out in a wash.


How does DNA and gel electrophoresis relate?

Gel electrophoresis separates an individual's DNA fragments from one another according to size. An electric current repels a mixture of the negatively-charged DNA fragments through microscopic pores in the gel from the negative to the positive electrode. Upon completion, the separated fragments of DNA can be visualized as a ladder of small bands in the gel by staining with a methylene blue dye solution or smaller DNA segments move more easily through the gel.

Related questions

What are the functions of the loading dye in electrophoresis how can DNA be prepared for visualization?

First, loading dye is meant to help weigh down the DNA solution, so that it can sink into the bottom of the wells and not float in the buffer solution.Second, two different types of loading dye are used in electrophoresis. One of them moves more quickly than most of your DNA fragments, and the other moves more slowly, helping you determine the relative position of your DNA, as it should be in between the two bars or dye. This also tells you when to stop electrophoresis so that your DNA does not fall out of your agarose gel.Note that loading dye does not bind to the DNA itself and does not allow you to see the bars of DNA usually seen in a complete DNA fingerprint.


What does dye contain?

The loading dye comprises bromophenol blue, Ficoll 400 and water majorly while Xylene cyanol, Tris and EDTA are optional in it. Bromophenol blue is one of the most popular indicators of DNA in agarose gel electrophoresis. Bromophenol blue is a pH indicator.


What is th blue dye added to the sample before the electrophoresis is performed?

In biochemistry labs, the traditional answer for a protein gel (polacrylamide gel electrophoresis) is bromphenol blue. For a DNA gel (agarose gel electrophoresis), traditionally the same dark blue dye bromphenol blue was combined with the lighter, slower migrating blue dye xylene cyanol. Oftentimes nowwe only use the bromphenol blue, or even substitute for it with Orange G, which is a UV-transparent dye that more easily enables the visualization of smaller molecular weight nucleic acids that migrate in the same region.


Definition of DNA loading dye?

Loading dye is a substance commonly used in labs and the study of genetics. It causes DNA to become clearer under a microscope by tinting it purple.


What does loading dye contain?

Some form of dye and glycerol to pull DNA down into the loading wells. A commonly used mixture is 0.25% bromophenol blue and 30% glycerol.


Function of agarose in agarose gel electrophoresis?

Agarose is used in gel electrophoresis to separate nucleic acids (like DNA) by size, charge an other physical properties. Gel electrophoresis uses an electrical current to make particles move. For example, DNA is negative, so it'll travel towards to positive electrode of the gel box. Agarose has small pores through which a DNA can travel. Bigger fragments of DNA travel shorter distances, because it takes longer for them to navigate through the pores of the agarose gel. Identically sized pieces of DNA will travel the same distance, which is why you get bands (DNA with loading dye) after you run a a gel.


Why was it important to stop the gel electrophoresis before the dye ran off the edge of the gel?

You would lose your DNA.


What is the purpose of a stain in electrophoresis?

I think the Question should be " What is the use of a dye in electrophoresis?" to be more specific, The normal dyes that are incorporated into the sample loading buffer in case of agarose gel is bromophenol blue and xylene cyanol.These are used to track the movement of the sample, so that we can stop the electrophoresis when the dye front is nearly 80%(can vary depending on the molecular weight of the sample) away from the well. In case of polyacrylamide gel electrophoresis the dye has many functions: gives density to the sample so that it sits properly in the well. SDS binds to the amino acid and makes it anionic, so that the movement of the sample is based on molecular weight, if not the charge of the protein will also influence the movement. it also helps us to track the movement of the sample. DTT or mercaptoethanol helps in the breaking of cysteine bonds.. That's it.. But the question is too broad and can be specific!!!!!!!!!1


Does DNA loading dye for agarose also contains tracking buffers?

Yes to dilute the dye we use tracking buffer in it some time


How do you dye clothes in a front-loading washing machine?

You dye clothes in a washing machine by buying the packets of dye at a store and then you pour it in and then you let it set and voila it is dyed after you tale it out and dry it.


Is there any difference between DNA and protein loading dye?

Yes, their components are different. Proteins loading dye besides bromophenol component for dying it has TRIS buffer, a reducing agent and SDS, which gives proteins a negative charge that lets them to migrate.


What is the purpose of the glycerol in the loading dye?

It gives density to the sample that we load and also it avoids diffusion of sample