answersLogoWhite

0

increasing the agarose concentration will enable the separation of smaller fragments of DNA. the structure of the gel (agarose) consists of crosslinks, therefore the higher the concentration of agarose the more crosslinks there will be and smaller size "holes" for the DNA to travel through (also the other way around, with less concentrated agarose)

User Avatar

Wiki User

16y ago

What else can I help you with?

Related Questions

What is a common name for gel electrophoresis?

Agarose gel electrophoresis.


Is agarose gel electrophoresis suitable for only gram negative plasmid DNA?

Agarose gel electrophoresis is suitable for ALL DNA.


What Is Agarose Solution?

Agarose solution is a gel-like substance used in molecular biology and biochemistry for techniques like agarose gel electrophoresis. It is derived from seaweed and forms a matrix in which DNA, RNA, and proteins can be separated based on size. The concentration of agarose in the solution determines the size range of molecules that can be effectively separated.


What gel is typically used in electrophoresis experiments?

The gel typically used in electrophoresis experiments is agarose gel.


Preparation of 1 percent agarose gel or How to prepare 1 percent agarose gel?

Check the answer for How do you make an electrophoresis gel?


What is agarose concentration?

Agarose concentration refers to the amount of agarose powder mixed with buffer solution to make a gel for DNA electrophoresis. Typical concentrations range from 0.5% to 2%, with higher concentrations providing better resolution for larger DNA fragments. The chosen concentration depends on the size of the DNA fragments being analyzed.


What has the author A J Houtsmuller written?

A. J. Houtsmuller has written: 'Agarose-gel-electrophoresis of lipoproteins' -- subject(s): Blood protein electrophoresis, Electrophoresis, Gel electrophoresis, Lipoproteins


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.


What is the purpose of using a buffer in agarose gel electrophoresis?

The purpose of using a buffer in agarose gel electrophoresis is to maintain a stable pH and provide ions that help conduct electricity, allowing the DNA or other molecules to move through the gel.


what is the gel in Gel Electrophoresis?

The gel in gel electrophoresis is typically made of agarose or polyacrylamide. It acts as a matrix to separate DNA, RNA, or proteins based on size and charge as an electric current passes through it. Agarose gels are commonly used for DNA analysis, while polyacrylamide gels are often used for higher resolution protein separation.


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 is the functions of UV transilluminator in genetic laboratory?

to vizualise DNA after Agarose gel electrophoresis