Denaturing Gradient Gel Electrophoresis
Yvonne Wallis
Abstract
Yvonne Wallis
Abstract
Denaturing gradient gel electrophoresis (DGGE) is a powerful mutation detection technique described by Fisher et al. in 1983 (). It allows the resolution of relatively large DNA fragments (usually polymerase chain reaction [PCR] products) differing by only a single nucleotide. DGGE is most frequently employed for the detection of unknown mutations. A related technique referred to as constant denaturing gradient gel electrophoresis (CDGE) is used for the sensitive detection of known mutations (),(). More recently a modified version of DGGE known as 2-dimensional DGGE has been employed for the simultaneous analysis of several PCR fragments (). PCR fragments are initially separated by size on a polyacrylamide gel prior to loading onto a conventional denaturing gradient gel system, as will be described in this chapter.
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Denaturing gradient gel electrophoresis (DGGE) is a powerful mutation detection technique described by Fisher et al. in 1983 (). It allows the resolution of relatively large DNA fragments (usually polymerase chain reaction [PCR] products) differing by only a single nucleotide. DGGE is most frequently employed for the detection of unknown mutations. A related technique referred to as constant denaturing gradient gel electrophoresis (CDGE) is used for the sensitive detection of known mutations (),(). More recently a modified version of DGGE known as 2-dimensional DGGE has been employed for the simultaneous analysis of several PCR fragments (). PCR fragments are initially separated by size on a polyacrylamide gel prior to loading onto a conventional denaturing gradient gel system, as will be described in this chapter.
Key concepts: Temperature gradient gel electrophoresis, Gel electrophoresis, Gel electrophoresis of nucleic acids, Molecular biology, Molecular-weight size marker, Electrophoresis, Polyacrylamide gel electrophoresis, Polymerase chain reaction