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Easy-Change® XL Site-Directed Mutagenesis Kit

For research use only. Not intended for any clinical use.
Cat.No.
SMK-Y001
Description
Creative Biogene's Easy-Change® XL Site-Directed Mutagenesis Kit allows site specific mutation in virtually any double-stranded plasmid, thus eliminating the need for subcloning into M13-based bacteriophage vectors and for ssDNA rescue. In addition, the Easy-Change® XL system requires no specialized vectors, unique restriction sites, or multiple transformations. This rapid four-step procedure generates mutants with greater than 80% efficiency. The protocol is simple and uses either miniprep plasmid DNA or cesium-chloride-purified DNA.
Applications
• Study of protein structure-function relationships and gene expression;
• Vector modification;
Features
• Designed for more efficient DNA replication and bacterial transformation.
• Allows sitespecific mutation in virtually any double-stranded plasmid.
• Requires no specialized vectors, unique restriction sites, or multiple transformations.
• Rapid four-step procedure generates mutants with greater than 80% efficiency.
Sample Type
DNA
Storage
Store at -20°C. When stored as directed, the product is stable for at least two years.

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Q & A

Customer Reviews

Customer Q&As
What is site-directed mutagenesis?

A: Site-directed mutagenesis is a laboratory technique used to introduce specific mutations or changes in a DNA sequence at a desired site. It involves altering the genetic code of a gene by introducing specific nucleotide changes to study the effects of these mutations on protein structure and function.

What is the efficiency of site-directed mutagenesis kit?

A: A mutagenesis efficiency >80% was consistently achieved in the case of two unrelated plasmids.

What are the benefits of site-directed mutagenesis?

A: Site-directed mutagenesis is a valuable tool for modifying genes and studying the structural and functional properties of proteins based on the structure, function, catalytic mechanism, and catalytic residues of enzymes. Site-directed mutations include single mutations and combination mutations.

Why are the desired mutations missing from my screened transformants?

A: Although this is not a common result, there are several known causes of background transformants: 1) too many plasmids in the PCR, 2) selection against specific DNA structures (such as inverted or tandem repeats), and 3) selection against the recombinant protein by the host E. coli cells.

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Customer Reviews
Worked very well

Extremely low error rate reduces screening time. Good experimental results were obtained.

United States

01/27/2022

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