5' C ↓ Y C G R G 3'
3' G R G C Y ↑ C 5'

Thermo Scientific FastDigest Eco88I restriction enzyme recognizes the C^YCGRG site and cleaves well within 5–15 minutes at 37°C using universal FastDigest buffer. Isoschiases: AvaI, Ama87I, BmeT110I, BsiHKCI, BsoBI.

Thermo Scientific FastDigest Eco88I is a premium line of fast restriction enzymes that are 100% active in both universal FastDigest and FastDigest Green reaction buffers.

Universal buffer allows rapid single, double or multiple enzyme digestion of DNA in 5–15 minutes without the need for buffer changes or subsequent DNA purification steps. See FastDigest Enzyme Reaction Conditions table for enzymatic activity, heat inactivation, and incubation of this and other FastDigest restriction enzymes time. DNA modifying enzymes (such as Klenow fragment, T4 DNA Ligase, alkaline phosphatase and T4 DNA Polymerase) are 100% active in FastDigest buffer. Therefore, enzymes used in downstream applications can be added directly to the FastDigest reaction mixture.

For convenience, FastDigest Green buffer includes 1 density reagent and 2 tracking dyes for loading digestion reaction products directly onto the gel.

Shorter incubation times and optimized universal FastDigest buffer composition eliminate star activity effects.

Features

• All FastDigest enzymes are 100% active in universal buffers
• 100% buffer compatible with downstream applications< br>• Complete digestion in 5–15 minutes
• Load directly onto gel
• No star activity
• 176 FastDigest enzymes available

Applications

• Molecular cloning
• Restriction site mapping
• Genotyping
• Southern blot
• Restriction fragment length polymorphism (RFLP)< br>• SNP Analysis

Note: FastDigest Green Buffer has the same high performance as colorless FastDigest Buffer in DNA digestion reactions and downstream applications. For applications requiring product analysis by fluorescence excitation (eg determination of concentration under UV light), the use of colorless FastDigest buffer is recommended.

See product specifications for information on methylation sensitivity.