B9027S,  Q5 Reaction Buffer Pack - 6.0 ml

B9027S, Q5 Reaction Buffer Pack - 6.0 ml

E0554S,  Q5 Site-Directed Mutagenesis Kit - 10 rxns

E0554S, Q5 Site-Directed Mutagenesis Kit - 10 rxns

E0552S, Q5 Site-Directed Mutagenesis Kit (Without Competent Cells) - 10 rxns

1.014,48 RON

The Q5® Site-Directed Mutagenesis Kit (Without Competent Cells) enables rapid, site-specific mutagenesis of double-stranded plasmid DNA in less than 2 hours.

SKU
NEB_E0552S

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

 

 

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Description

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