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Where agarose gels are best for running larger molecules, like DNA, SDS-PAGE is better suited for running smaller ones, like proteins.

SDS-PAGE has a number of uses, which include:

* Establishing protein size

* Protein identification

* Determining sample purity

* Identifying disulfide bonds

* Quantifying proteins

* Blotting applications

SDS-PAGE stands for sodium dodecyl (lauryl) sulfate-polyacrylamide gel electrophoresis. The SDS portion is a detergent. You may recognize it if you read the ingredients lists on your shampoo, soap, or toothpaste. The purpose of the SDS detergent is to take the protein from its native shape, which is basically a big glob, and open it up into a linear piece. It's kind of like taking a wadded up ball of string and untangling it into one straight, long piece. This will allow it to run more efficiently down the gel and will get you better results, since it's easier to compare two linear pieces of something rather than two wads of the same thing.

In more scientific terms, it is an anionic detergent that binds quantitatively to proteins, giving them linearity and uniform charge, so that they can be separated solely on the basis if their size. The SDS has a high negative charge that overwhelms any charge the protein may have, imparting all proteins with a relatively equal negative charge. The SDS has a hydrophobic tail that interacts strongly with protein (polypeptide) chains. The number of SDS molecules that bind to a protein is proportional to the number of amino acids that make up the protein. Each SDS molecule contributes two negative charges, overwhelming any charge the protein may have. SDS also disrupts the forces that contribute to protein folding (tertiary structure), ensuring that the protein is not only uniformly negatively charged, but linear as well.

The polyacrylamide gel electrophoresis works in a similar fashion to an agarose gel, separating protein molecules according to their size. In electrophoresis, an electric current is used to move the protein molecules across a polyacrylamide gel. The polyacrylamide gel is a cross-linked matrix that functions as a sort of sieve to help "catch" the molecules as they are transported by the electric current. The polyacrylamide gel acts somewhat like a three-dimensional mesh or screen. The negatively charged protein molecules are pulled to the positive end by the current, but they encounter resistance from this polyacrylamide mesh.

The smaller molecules are able to navigate the mesh faster than the larger one, so they make it further down the gel than the larger molecules. This is how SDS-PAGE separates different protein molecules according to their size. Once an SDS-PAGE gel is run, you need to fix the proteins in the gel so they don't come out when you stain the gel. Acetic acid 25% in water is a good fixative, as it keeps the proteins denatured. The gel is typically stained with Coomasie blue dye R250, and the fixative and dye can be prepared in the same solution using methanol as a solvent. The gel is then destained and dried.

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Why p53 is run as 53 kda on sds page?

p53 is detected as approximately 53 kDa on SDS-PAGE because it is a 53 kilodalton (kDa) protein. SDS-PAGE separates proteins based on size, so the molecular weight of p53 corresponds to the band observed at 53 kDa on the gel.


What is sds-page used for?

SDS-PAGE (sodium dodecyl sulfate polyacrylamide gel electrophoresis) is a common technique used to separate proteins based on their molecular weight. It denatures the proteins and binds a negative charge to them, allowing for separation solely based on size. It is often used in biochemistry and molecular biology research to analyze protein composition and purity.


What is Laemmli gels?

Laemmli gels are a type of polyacrylamide gel used in protein electrophoresis. They are commonly used in the separation of proteins based on their size during techniques such as SDS-PAGE. Laemmli gels are named after the scientist who developed the gel electrophoresis technique, Ulrich K. Laemmli.


Why to use dissolving gel in SDS-PAGE?

Dissolving gel in SDS-PAGE serves to separate proteins based on their size, allowing for effective analysis of protein samples. The gel matrix, composed of polyacrylamide, provides a porous environment that facilitates the migration of proteins when an electric current is applied. By using a dissolving gel, researchers can achieve higher resolution in protein separation and facilitate subsequent applications such as Western blotting or mass spectrometry for protein identification. Additionally, it ensures the proteins are denatured and uniformly charged, which is crucial for accurate size determination.


Are SDS and SDS-plus bits the same?

The short answer to your question is "yes". I found myself researching the same question a few days ago and found that the real difference is between SDS/SDS Plus and SDS Max. I don't recall the exact dimension now, so I won't try to quote it, but the Max is a larger size. The answer I found was enough to tell me I used SDS (SDS Plus), and those were the bits I needed to buy. Once I knew that, I didn't need to remember the size of SDS Max...they were too big for my drill. Last point, SDS Plus is sometimes shortened to SDS+.

Related Questions

Why is denaturing sds-page used for running sds-page electrophoresis of egg-white lysozyme and not non-denaturing page?

may be because of toomany disulfide linkages


What are the differences between SDS and SDS Max drill bits and which one is more suitable for heavy-duty drilling applications?

SDS and SDS Max drill bits differ in their size and power. SDS Max drill bits are larger and more powerful, making them more suitable for heavy-duty drilling applications. They can handle tougher materials and larger holes compared to SDS drill bits.


What are the key differences between SDS Plus and SDS Max drill bits, and which one would be more suitable for heavy-duty drilling applications?

The key differences between SDS Plus and SDS Max drill bits are their size and power. SDS Max drill bits are larger and more powerful than SDS Plus drill bits, making them more suitable for heavy-duty drilling applications.


Why p53 is run as 53 kda on sds page?

p53 is detected as approximately 53 kDa on SDS-PAGE because it is a 53 kilodalton (kDa) protein. SDS-PAGE separates proteins based on size, so the molecular weight of p53 corresponds to the band observed at 53 kDa on the gel.


What are the key differences between SDS Max and SDS drills, and which one is more suitable for heavy-duty drilling applications?

SDS Max drills are larger and more powerful than SDS drills, making them better suited for heavy-duty drilling applications. The key differences lie in their size and power, with SDS Max drills being able to handle larger and tougher drilling tasks compared to SDS drills.


What are the key differences between SDS Max and SDS Plus drill bits, and which one would be more suitable for heavy-duty drilling applications?

The key differences between SDS Max and SDS Plus drill bits are their size and power. SDS Max drill bits are larger and more powerful, suitable for heavy-duty drilling applications. They can handle larger holes and tougher materials compared to SDS Plus drill bits, which are smaller and less powerful. For heavy-duty drilling applications, SDS Max drill bits would be more suitable due to their increased size and power.


What are the differences between agarose gel electrophoresis and SDS-PAGE techniques for separating and analyzing biomolecules?

Agarose gel electrophoresis separates biomolecules based on size and charge, while SDS-PAGE separates based on size and mass. Agarose gel is used for larger molecules like DNA and RNA, while SDS-PAGE is used for proteins. Agarose gel uses a gel made from agarose, while SDS-PAGE uses a gel made from polyacrylamide.


What test has replaced the radial immunodiffusion test?

SDS-PAGE method


Who discovered SDS PAGE electrophoresis?

SDS-PAGE electrophoresis was developed by biochemist Ulrich K. Laemmli in 1970. It is a widely used technique for separating proteins based on their molecular weight.


What is difference between sds page and western blotting?

SDS-PAGE is a technique used to separate proteins based on their size, while western blotting is a technique used to detect specific proteins in a sample using antibodies. In SDS-PAGE, proteins are separated by gel electrophoresis, while in western blotting, proteins are transferred from a gel to a membrane for detection using antibodies.


What method could you use to further separate two bands from the same protein fraction after SDS-PAGE?

Electrophoresis is the method that could be used to further separate two bands from the same protein fraction after SDS-PAGE.


What the difference between sds and sds max drills?

SDS (Slotted Drive System) and SDS Max drills differ primarily in their shank sizes and applications. SDS drills typically have a smaller, lighter design suited for light to medium-duty tasks, while SDS Max drills feature a larger, more robust shank, allowing for heavier-duty work and greater impact energy. Additionally, SDS Max tools can accommodate larger drill bits and chisels, making them ideal for more demanding concrete and masonry applications. Overall, the choice between the two depends on the scale and intensity of the project.