McrBC specifically cleaves DNA containing methyl cytosine (mC: 5-hydroxymethylcytosine, 5-methylcytosine, 4-methylcytosine) preceded by a purine nucleotide (Pu: A or G). DNA cleavage by McrBC requires at least two PumC sites within a distance of 40–2,000 bp.
Overview
Source: recombinant proteins expressed in E. coli
Concentration: 1 unit /µl
Supplied buffer: McrBC
Reaction temperature: 37°C
Substrate for unit definition: pBR322
Effect of DNA methylation: This enzyme specifically cleaves DNA containing methyl cytosine (mC : 5-hydroxymethylcytosine, 5-methylcytosine, 4-methylcytosine) preceded by a purine nucleotide (Pu: A or G). DNA cleavage by McrBC requires at least two PumC sites within a distance of 40–2,000 bp.
Applications
DNA methylation analysis (qAMP: quantitative analysis of DNA methylation using real-time PCR)
Enrichment of unmethylated DNA (CHARM: Comprehensive high-throughput arrays for relative methylation)
McrBC specifically cleaves DNA containing methyl cytosine (mC: 5-hydroxymethylcytosine, 5-methylcytosine, 4-methylcytosine) preceded by a purine nucleotide (Pu: A or G). DNA cleavage by McrBC requires at least two PumC sites within a distance of 40–2,000 bp.
Overview
Source: recombinant proteins expressed in E. coli
Concentration: 1 unit /µl
Supplied buffer: McrBC
Reaction temperature: 37°C
Substrate for unit definition: pBR322
Effect of DNA methylation: This enzyme specifically cleaves DNA containing methyl cytosine (mC : 5-hydroxymethylcytosine, 5-methylcytosine, 4-methylcytosine) preceded by a purine nucleotide (Pu: A or G). DNA cleavage by McrBC requires at least two PumC sites within a distance of 40–2,000 bp.
Applications
DNA methylation analysis (qAMP: quantitative analysis of DNA methylation using real-time PCR)
Enrichment of unmethylated DNA (CHARM: Comprehensive high-throughput arrays for relative methylation)