The Q5® Site-Directed Mutagenesis Kit (Without Competent Cells) enables rapid, site-specific mutagenesis of double-stranded plasmid DNA in less than 2 hours.
The Q5® Site-Directed Mutagenesis Kit (Without Competent Cells) enables rapid, site-specific mutagenesis of double-stranded plasmid DNA in less than 2 hours.
Non-overlapping primer design ensures robust, exponential amplification, generating a high percentage of desired mutations from a wide range of templates
Intramolecular ligation and transformation into NEB high-efficiency competent cells results in high colony yield
Extremely low error rate of Q5 Hot Start High-Fidelity DNA Polymerase reduces screening time
Hot start polymerase enables room temperature reaction setup
DpnI background reduction permits a wide range of starting template concentrations
Use of standard primers eliminates additional expenses from phosphorylated or purified oligos
Easy-to-use PCR master mix and unique multi-enzyme KLD mix offer convenience and quality
Rapid and direct treatment step proceeds at room temperature in 5 minutes
Allows the use of any chemically-competent E. coli cells suitable for cloning
Use NEBaseChanger to generate primer sequences and an annealing temperature
Materials Required but not Supplied
Chemically-competent E. coli cells
SOC Outgrowth Media
Selection Plates
Advantages and Features
Non-overlapping primer design ensures robust, exponential amplification, generating a high percentage of desired mutations from a wide range of templates
Intramolecular ligation and transformation into NEB high-efficiency competent cells results in high colony yield
Extremely low error rate of Q5 Hot Start High-Fidelity DNA Polymerase reduces screening time
Hot start polymerase enables room temperature reaction set-up
DpnI background reduction permits a wide range of starting template concentrations
Use of standard primers eliminates additional expenses from phosphorylated or purified oligos
Easy-to-use PCR master mix and unique multi-enzyme KLD mix offer convenience and quality
Rapid and direct treatment step proceeds at room temperature in 5 minutes
Allows the use of any chemically-competent E. coli cells suitable for cloning
The Q5® Site-Directed Mutagenesis Kit (Without Competent Cells) enables rapid, site-specific mutagenesis of double-stranded plasmid DNA in less than 2 hours.
Non-overlapping primer design ensures robust, exponential amplification, generating a high percentage of desired mutations from a wide range of templates
Intramolecular ligation and transformation into NEB high-efficiency competent cells results in high colony yield
Extremely low error rate of Q5 Hot Start High-Fidelity DNA Polymerase reduces screening time
Hot start polymerase enables room temperature reaction setup
DpnI background reduction permits a wide range of starting template concentrations
Use of standard primers eliminates additional expenses from phosphorylated or purified oligos
Easy-to-use PCR master mix and unique multi-enzyme KLD mix offer convenience and quality
Rapid and direct treatment step proceeds at room temperature in 5 minutes
Allows the use of any chemically-competent E. coli cells suitable for cloning
Use NEBaseChanger to generate primer sequences and an annealing temperature
Materials Required but not Supplied
Chemically-competent E. coli cells
SOC Outgrowth Media
Selection Plates
Advantages and Features
Non-overlapping primer design ensures robust, exponential amplification, generating a high percentage of desired mutations from a wide range of templates
Intramolecular ligation and transformation into NEB high-efficiency competent cells results in high colony yield
Extremely low error rate of Q5 Hot Start High-Fidelity DNA Polymerase reduces screening time
Hot start polymerase enables room temperature reaction set-up
DpnI background reduction permits a wide range of starting template concentrations
Use of standard primers eliminates additional expenses from phosphorylated or purified oligos
Easy-to-use PCR master mix and unique multi-enzyme KLD mix offer convenience and quality
Rapid and direct treatment step proceeds at room temperature in 5 minutes
Allows the use of any chemically-competent E. coli cells suitable for cloning